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Human germ/stem cell-specific gene TEX19 influences cancer cell proliferation and cancer prognosis
Molecular Cancer volume 16, Article number: 84 (2017)
Cancer/testis (CT) genes have expression normally restricted to the testis, but become activated during oncogenesis, so they have excellent potential as cancer-specific biomarkers. Evidence is starting to emerge to indicate that they also provide function(s) in the oncogenic programme. Human TEX19 is a recently identified CT gene, but a functional role for TEX19 in cancer has not yet been defined.
siRNA was used to deplete TEX19 levels in various cancer cell lines. This was extended using shRNA to deplete TEX19 in vivo. Western blotting, fluorescence activated cell sorting and immunofluorescence were used to study the effect of TEX19 depletion in cancer cells and to localize TEX19 in normal testis and cancer cells/tissues. RT-qPCR and RNA sequencing were employed to determine the changes to the transcriptome of cancer cells depleted for TEX19 and Kaplan-Meier plots were generated to explore the relationship between TEX19 expression and prognosis for a range of cancer types.
Depletion of TEX19 levels in a range of cancer cell lines in vitro and in vivo restricts cellular proliferation/self-renewal/reduces tumour volume, indicating TEX19 is required for cancer cell proliferative/self-renewal potential. Analysis of cells depleted for TEX19 indicates they enter a quiescent-like state and have subtle defects in S-phase progression. TEX19 is present in both the nucleus and cytoplasm in both cancerous cells and normal testis. In cancer cells, localization switches in a context-dependent fashion. Transcriptome analysis of TEX19 depleted cells reveals altered transcript levels of a number of cancer-/proliferation-associated genes, suggesting that TEX19 could control oncogenic proliferation via a transcript/transcription regulation pathway. Finally, overall survival analysis of high verses low TEX19 expressing tumours indicates that TEX19 expression is linked to prognostic outcomes in different tumour types.
TEX19 is required to drive cell proliferation in a range of cancer cell types, possibly mediated via an oncogenic transcript regulation mechanism. TEX19 expression is linked to a poor prognosis for some cancers and collectively these findings indicate that not only can TEX19 expression serve as a novel cancer biomarker, but may also offer a cancer-specific therapeutic target with broad spectrum potential.
The ability of cancer cells to self-renew and undergo phenotypic changes has led to the postulate that some have similarities to germline cells and/or stem cells [1, 2], leading to the suggestion that a key feature of oncogenesis is a cellular soma-to-germline transition [1, 3,4,5,6]. This is supported by the finding that tumours in Drosophila melanogaster activate a large cohort of germline genes during oncogenesis and that some of these are essential for tumour progression [7,8,9]. Analysis of gene expression in human tumours indicates that a similar pattern of germline gene activation is also apparent, inferring a possible functional requirement .
One major group of germline genes is termed the cancer/testis (CT) genes. These encode cancer/testis antigens (CTAs), proteins that are normally only present in healthy adult testis, but are also found in a wide range of cancers [10,11,12]. Little is currently known about the function in the testis for most of these proteins, but evidence is emerging to indicate that CTAs function in oncogenic processes, supporting the idea of a functional soma-to-germline transition [12, 13]. Examples include regulation of cellular mitotic fidelity [14,15,16,17,18,19,20] and invasiveness [21,22,23,24,25]. These findings offer attractive new avenues for cancer-specific therapeutic targeting via inhibition of oncogenic CTA functions [2, 11,12,13].
Recently, a pipeline for the identification of new CT genes was developed [26, 27]. One of the genes identified was Testis Expressed 19 (TEX19), a mammalian specific gene with a poorly defined function [28, 29]; subsequently, this expression profile was verified  and TEX19 protein was shown to be a CTA .
In rodents, the TEX19 orthologue has undergone duplication to generate a paralogue pair of genes, Tex19.1 and Tex19.2 . Both murine genes are differentially expressed, with Tex19.2 expression restricted to the developing gonadal ridge and adult testis and Tex19.1 being expressed in the adult testis, the placenta and in the early embryo, in a pattern matching the pluripotency marker gene Oct4 , although expression control mechanisms of the two genes is distinct . Tex19.1 is expressed in embryonic stem cells (ESCs) and whilst this might infer a functional role in stemness , Tex19.1-/- ESCs have no overt stemness/ proliferative defects , nor are there any overt phenotypic defects in spermatagonial germ cells . Preliminary analysis of human TEX19 expression indicates it is orthologous to Tex19.1 as it is expressed in human ESCs . Tex19.1 is largely cytoplasmic and appears to be located in spermatagonial germline cells of testis seminiferous tubules, with levels diminishing as cells differentiate during spermatogenesis, suggesting a germline-specific function [29, 33, 34].
Tex19.1 -/- mice are viable with no apparent behavioural defects [33,34,35]. There is a slight increase in mortality of pups older than 5 days post-partum, but this has been attributed to in utero developmental defects linked to placental dysfunction [33, 35]. Female fertility of Tex19.1 -/- mice has been independently reported to be reduced  and normal , with the discrepancy being attributed to distinct genetic backgrounds . Males exhibit sub-normal levels of fertility with considerable inter-individual differences in spermatogenesis indicating a phenotypic variability, the cause of which is unknown [33, 34]. Meiosis in Tex19.1 -/- males has defects, which include impaired meiotic chromosome synapsis, the persistence of unprocessed DNA double-strand breaks, increased apoptosis and post pachytene meiosis I chromosome segregation defects, although these were not uniformly apparent [33, 34]. Analysis of gene expression during early spermatogenesis did not reveal any notable changes to genes that could directly influence meiosis, but there was significant elevation in the expression of the class II long terminal repeat (LTR)-retrotransposon MMERVK10C [33, 34]. Expression of other transposable elements (TEs), such as LINEs, SINEs and IAP retrotransposons did not appear to be altered, indicating TE specific suppressor activity for Tex19.1 in testis, which is proposed to be distinct from the Piwi-mediated pathway for TE regulation .
The proposal that Tex19.1 functions in an independent TE regulatory pathway is further supported by the finding that in murine placenta, where there are alterations to expression levels of some TEs, Tex19.1 is the only known methylation-sensitive genome defense gene that is highly expressed , suggesting it may independently serve to protect placental cells from elevated TE expression . Female Tex19.1 -/- mutant mice also exhibit impaired placental function [33, 35]. Unlike Tex19.1 -/- male testis tissue, Tex19.1 -/- placental tissue exhibits elevated LINE expression and also exhibits some differential expression of protein coding genes . Collectively, these findings suggest that Tex19.1 controls transcription/transcript related mechanisms to protect the germline and placental genomes [29, 33,34,35].
The finding that human TEX19 is a CT gene opens the question of whether TEX19 expression is oncogenic or provides a functional advantage to cancer cells [26, 31]. Expression of germline genes has been linked to poor patient prognosis in cancers, such as lung cancer (for example, see ), so revealing functional roles of these genes, if any, is important to understand the mechanisms of cancer development/progression. In this study we identify a requirement for TEX19 in human cancer cells to drive proliferation that reveal it to be a potential cancer-specific drug target and prognostic indicator.
Cell culture and proliferation/self-renewal assays
Human cacner cell lines used in this study are provided in Additional file 1; Table S1. Cells were cultured in McCoy’s 5A medium (Thermo Fisher Scientific, Runcorn, UK) supplemented with 10% fetal bovine serum (FBS; Life Technologies) or in RPMI medium supplemented with 10% FBS and 2 mM sodium pyruvate (Thermo Fisher Scientific, Runcorn, UK); SW480 cells were cultured in Dulbecco’s modified Eagle’s Medium (Thermo Fisher Scientific, Runcorn, UK).. All cells were cultured at 37 °C in 5% CO2 in a humidified incubator. All cells were authenticated once every 12 months using LGC Standards Cell Line Authentication service (last report number: 710236782; Teddington, UK). Cells were regularly checked for mycoplasma using the LookOut Mycoplama Detection Kit (Sigma, Irvine, UK).
For leptomycin B (LMB) treatment cells were seeded into 40 mm tissue culture dishes and grown to the required density. Cells were then treated with 10 ng/ml LMB (L2913; Sigma, Irvine, UK) and incubated for a further 16 h.
Extreme limiting dilution analysis (ELDA) was performed as previously described [37, 38]. Briefly, sphere-derived cell were collected from 10 cm dishes and diluted into single cell suspension and plated at concentrations of 1000 to 1 cells per 100 μl SCM using repeats of defined experimental conditions in 96 well ultra-low attachment plates (Costar Corning; Sigma, Irvine, UK). Cells were incubated at 37 °C in a 5% CO2 atm for 10 days. Cells were supplemented with 50 μl of stem cell media (SCM) and transfection complexes re-applied after 4 and 8 days of incubation. At the end of 10 days the number of wells showing spheres with more than 20 cells were counted by light microscope. ELDA web tool (hrrp://bioinf.wehi.edu.au/software/elda) was used to determine frequencies of sphere forming cells.
Staining for senescence was carried out using β-galactosidase Staining Kit (Cell Signaling, Leiden, Holland) following the manufacturer’s instructions.
siRNAs used in this study are TEX19 siRNA A (5′-AGGATTCACCATAGTCTCTTA-3′), TEX19 siRNA B (5′-TTCAACATGGAGATCAGCTAA-3′) and a negative control (Qiagen, Manchester, UK, Allstars Negative Control siRNA). Transfection was carried out with HiPerFect (Qiagen, Manchester, UK) following the manufacturer’s instructions. Briefly, 150 ng of siRNA was mixed with 6 μl of HiPerFect and 100 μl of cell specific medium. This mix was incubated at room temperature for 15 min to permit transfection complexes to form and was then added in a dropwise fashion to approximately 1.5 × 105 cells. The number of siRNA treatments per cell culture was dependent upon the specific experiment and siRNA was added to cells at least once every 24 h for proliferation assays over extended periods. Depletion was verified by RT-qPCR and/or western blotting.
Whole cell extraction, fractionation and western blotting
Whole-cell lysates were prepared using M-PER lysis buffer (Thermo Fisher Scientific, Runcorn, UK #78503), Halt Protease Inhibitor Cocktail (Thermo Fisher Scientific, Runcorn, UK) and Halt Phosphatase Inhibitor Cocktail (Thermo Fisher Scientific, Runcorn, UK). Approximately 30 μg of protein extract were used for western blotting (WB). Samples were mixed with 2X Laemmli Buffer (1:1) (Sigma, Irvine, UK; S3401) and boiled at 100 °C for 5 min prior to electrophoresis. Precision Plus Protein Dual Color Standards (BioRad, Watford, UK) was used as a protein ladder. NuPAGE Novex 4–12% Bis-Tris gels (Thermo Fisher Scientific, Runcorn, UK) were used and electrophoresis was carried out in NUPAGE MOPS SDS buffer (Thermo Fisher Scientific, Runcorn, UK) for 90 min at 120 v. Fast Western Blot Kit, ECL substrate (Thermo Fisher Scientific, Runcorn, UK) was used according to manufacturer’s instructions to detect the primary antibodies. Membranes were probed with primary antibodies in 10% dry milk/PBS/0.5% Tween 20. Incubation with secondary antibodies was performed at room temperature for 1 h, followed by a 10 min wash in milk solution and 3 additional 10 min washes in PBS/0.5% Tween 20 at room temperature. Antibody detection was performed using Pierce ECL Plus Western Blotting Substrate (Thermo Fisher Scientific, Runcorn, UK).
Subcellular fractionation was carried out as follows. Following harvesting cells were resuspended in hypotonic buffer [50 mM Tris-HCl (pH 7.4), 0.1 M sucrose, 1 mM AEBSF] and lysis buffer C (1% Triton, 10 mM MgCl2, 1 mM AEBSF) at 1:1 ratio. Following incubation on ice for 30 min tubes were spun at 6000 g for 2 min. Supernatant contained cytoplasmic proteins and the pellet was resuspended in lysis buffer N [50 mM Tris-HCl (pH 7.4), 100 mM potassium acetate, 1 mM AEBSF] to extract nuclear protein.
The following antibodies were used in this study: anti-TEX19 (R & D Systems, AF6319), 1:200 dilution for WB; anti-Lamin B1 (Abcam, AB16048), 1:1000 dilution for WB; anti-tubulin (Sigma, T6074), 1:8000 dilution for WB; anti-cleaved caspase-3 (Cell Signaling, Leiden, Holland; 9664), 1:1000 dilution for WB; cell cycle cocktail (anti-pCDK2, anti-Actin, anti-pH3) (Abcam, Cambridge, UK; AB136810), 1:250 dilution for WB; anti-rabbit secondary antibody (Cell Signaling, Leiden, Holland; 7074), 1:3000 dilution for WB; anti-mouse secondary antibody (Cell Signaling, Leiden, Holland; 7076).
For the chromatin association assay (Ch) protein lysates were prepared consecutively with increased concentrations of NaCl. Protein extracts were subjected to western blotting as described using anti-a-tubulin and anti-histone H3 antibodies in addition to anti-TEX19 antibodies. 10 ng/ml KaryoMAX colcemid (Gibco, Runcorn, UK; 15212-012) was added to the growth medium to synchronize cells in metaphase prior to chromatin extraction.
Reverse transcription quantitative polymerase chain reaction (RT-qPCR)
Total RNA was extracted from appropriate cell cultures using the RNeasy Plus Mini Kit (Qiagen, Manchester, UK) following the manufacturer’s instructions. First-strand cDNA synthesis was carried out using SuperScript III First-Strand Synthesis System (Thermo Fisher Scientific, Runcorn, UK) following the manufacturer’s instructions.
qPCR reactions were carried out using GoTaq qPCR Master Mix (Promega, Southampton, UK) in a CFX96 Real-Time PCR Detection System C100 thermal cycler (BioRad, Watford, UK). All RT-qPCR primers were obtained from Qiagen (Manchester, UK). The exceptions were the HERV primers and primers for PIWIL3 and PIWIL4. PIWIL3 primers were PIWIL3F (5′-TGGCATTGCATTAAGTAAGGG-3′) and PIWIL3R (5′-TTTGAAAAACGCAAACATCG-3′). PIWIL4 primers were PIWIL4F (5′-CTGAAGGATACAGCGGGAAA-3′) and PIWIL4R (5′-AAAGATGCACTCAGCAAGGAC-3′). HERV primers are listed in Additional file 2; Table S2; other RT-qPCR primers are shown in Additional file 3; Table S3. Reactions were carried out in triplicate with PCR primers at a final concentration of 0.2 μM in a final volume of 25 μl. All PCR primers are available upon request. BioRad CFX Manager 2.0 software was used to determine primer efficiency/specificity, threshold cycle values (Ct values) and expression values using default parameters. Results were normalized using two or three reference genes and fold-change values were calculated based on the ΔΔCT method.
RNA sequencing and data analysis
Total RNA was extracted using RNeasy Plus mini kit (Qiagen, Manchester, UK) according to the manufacturer’s protocol. RNA quality was checked on an Agilent Bioanalyzer RNA 6000 nano chip and was assessed to be of high quality (RIN > 9.8). Indexed sequencing libraries were then prepared using the Illumina TruSeq v2 protocol. Briefly, polyA-tailed RNA enriched on oligo-dT beads before fragmentation and random priming. Reverse transcription was carried out with second strand synthesis and the resultant double-stranded cDNA was end repaired, A-tailed and Illumina TruSeq adapters were ligated. Correctly ligated fragments were enriched by performing 12 cycles of PCR with primers complementary to the Illumina adapters. The final libraries were checked and quantified on the Agilent Bioanalyzer DNA 1000 chip and the Life Technologies Qubit High Sensitivity DNA assay system before being pooled to an equimolar concentration of approximately 10 nM. qPCR was performed on a 105 dilution of the multiplex pool (Kapa Biosystems Library Quantification Kit; Sigma, Irvine, UK) before 12 pM of multiplex library was sequenced on one lane of an Illumina HiSeq (TruSeq v3 chemistry) generating 190 million reads passing filter. Reads were demultiplexed and fastq files generated using Illumina CASAVA v1.8.2 software.
Fastq data underwent guided alignment to the human genome (NCBI Build 37.2) using Tophat v2.0.6  with default parameters. Read duplicates were removed using Picard (http://broadinstitute.github.io/picard) and counts per gene generated using HTSeq . Differential expression at both the gene and exon level was carried out in R (https://www.r-project.org/) using the ‘DESeq’ and DEXSeq’ R packages . The resulting P values were adjusted for multiple testing with Benjamini and Hochberg’s  method to control the false discovery rate. Genes with a P value <0.05 and a log2-fold change > 1.0 have been selected as significant. Pathway and gene ontology (GO) analysis was carried out in R v3.2.3 (https://www.r-project.org/) using the ‘GOstats’ R package .
Fluorescence activated cell sorting cell cycle analysis
Following trypsinization cells were fixed in 70% ethanol at 4 °C overnight. Fixed cells were treated with 0.5 mg/ml RNase A (Sigma, Irvine, UK) and stained with propidium iodide (500 nM, Sigma, Irvine, UK). Stained cells were analyzed using a Partec CyFlow Cube 8 and cell cycle analysis was carried out using FCS Express 4 software.
Immunohistochemistry (IHC) and human tissue
Human tissue was obtained from patients following the guidelines of the North Wales Research Ethics Committee – West. All tissues were fixed in formalin, embedded in paraffin and prepared as 4 mm slices. Tumour/normal tissue arrays were obtained from the Cooperative Human Tissue Network (University of Virginia, USA). Staining was automated using the Ventana Benchmark XT instrument. Chromogenic reactions were carried out using 3,3′-diaminobenzidine and slides were counter stained with haematoxylin. The rabbit polyclonal anti-TEX19 antibody (Abcam, Cambridge, UK; 185507) was used for TEX19 staining. Secondary antibody only staining was used as a control. Antigen retrieval consisted of 4 min wash with protease I. All slides were scanned using and Axio Scanner.Z1 Scanner (Zeiss Cambridge, UK).
Tissue/cell immunofluorescence imaging
For staining of cultured cells 105 cells were seeded on a cover slip in a 24-well plate with appropriate medium and grown to the required density. Cells were fixed in 4% paraformaldehyde in PBS for 10 min at room temperature and then washed three times with PBS at room temperature. Cells were incubated for 1 h in 5% FBA/0.3% Triton in PBS at room temperature. Cells were incubated with primary antibodies in 1% BSA/0.3% Triton in PBS at appropriate concentrations overnight at 4 °C. Following three 5 min washes in PBS appropriate concentrations of the required secondary antibody were incubated with the cells in the same buffer for 1 h at room temperature in the dark. Following final washing cover slips were mounted on slides with Vectashiled Hard Set Antifade Mounting Medium (Vector Laboratories, Peterborough, UK) and counter stained with DAPI (Sigma) as required. Images were acquired using a Zeiss LSM 710 confocal microscope and analyzed using ZEN software (Zeiss, Cambridge, UK).
For tissue staining 4 μM paraffin embedded section were deparaffinised and re-hydrated as follows: three times through xylene, two times through 100% ethanol, two times through 70% ethanol, two times through sterile distilled H2O. Antigen retrieval was performed by heating samples in boiling 10 nM sodium citrate buffer (pH 6.0) for 10 min and cooling slides to room temperature. Slides were washed in sterile distilled water and stained as for the cultured cells (see above).
Antibodies used for staining were as follows, anti-TEX19 (Abcam, Cambridge, UK; AB185507), dilution of 1:50; anti-MAGE-A1 (LSBio, Nottingham, UK; LS-C87868), dilution of 1:20; anti-vimentin (LSBio, Nottingham, UK; LS-B7191), dilution of 1:100; secondary goat anti-rabbit (Alexa Fluor 488; Thermo Fisher Scientific, Runcorn, UK; A11034), dilution of 1:1,1000; secondary goat anti-mouse (Alexa Fluor 568; Thermo Fisher Scientific, Runcorn, UK; A11031), dilution of 1:1000.
Mouse tumourgenicity assay
In vivo tumour growth capability of Tex19shRNA-SW480-c3 cells was assessed by sub-cutaneous xenograft into immune deficient NSG mice (Envigo, Derby, UK). Cells were harvested using 1 mM EDTA and re-suspended at a density of 5 × 107 cells/ml in serum free DMEM medium. A total of 5 × 106 cells were injected sub-cutaneously into the flank of each mouse. Cells were allowed to establish for 6 days prior to induction of shRNA expression with doxycycline. To induce shRNA expression, mice were injected with 10 mg/kg intra-peritoneally every 2 days. Mice were then monitored, and when palpable, tumour volume was measured twice weekly with a digital caliper. Relative tumour volume (RTV) was calculated using xy2/2; where x is the longest axis of the tumour and y is the shortest axis of the tumour.
Cancer data sets available from The Cancer Genome Atlas (TCGA; http://cancergenome.nih.gov) were analyzed using R v3.2.3 (https://www.r-project.org/) to assess the association of TEX19 expression and clinical data. Normalized gene RSEM values for all TCGA RNA-seq data sets as well as corresponding clinical data were downloaded from http://firebrowse.org. The survival analysis was carried out on primary tumour samples apart from leukaemia, where the primary blood derived cancer samples from peripheral blood were used. Normalized RSEM values were transformed to log2 counts per million prior to survival analysis using voom  in the ‘limma’ R package . The patients were categorized in to two groups, low and high TEX19 expression in cancer, split by the median value. Overall survival (in years) related to TEX19 expression was computed with the Kaplan-Meier method and compared by the log rank test using the ‘survival’ R package . P values of <0.05 were considered statistically significant.
TEX19 is required for the proliferation and self-renewal of human cancer cells
Given the finding that TEX19 is expressed in a range of cancers (http://cancergenome.nih.gov/)  and the finding that other CT genes play a role in oncogenesis (for example, see ), we set out to determine whether TEX19 contributes to proliferative potential of human cancer cells. We chose colon cancer cell line SW480 as our primary model system as these cells are enriched for cancer-stem-like cells. Other cells lines previously shown to express TEX19 , including an additional colon line (HCT116) as well as a lung cancer line (H460) and an embryonal cancer line (NTERA2), were also employed to assess potential universality of proliferative and/or functional role(s) for TEX19. In these cell lines siRNA-depletion of TEX19 (using independent siRNAs) results in an inhibition of proliferation (Fig. 1a; Additional file 4: Figure S1a-d; siRNA-mediated TEX19 depletion was confirmed by RT-qPCR and western blotting, examples given in Fig. 1a; Additional file 4: Figure S1; western blots also validate the anti-TEX19 antibody).
TEX19 expression is found in germ cells/ESCs, and murine Tex19.1 has been linked to ESC self-renewal . To determine whether human TEX19 functions in self-renewal in cancer stem/progenitor cells, we carried out extreme limiting dilution assays (ELDA) to determine self-renewal ability in sphere-derived SW480 cells and NTERA2 cells . Cultures treated with independent siRNAs had reduced sphere formation from single cells (Fig. 1b; Additional file 5: Figure S2). This demonstrates that TEX19 is required for proliferation/self-renewal of cancer cells, which could infer such a role in germ and stem cells. Over expression of TEX19 in SW480 cells using a doxycycline inducible TEX19 did not further accelerate proliferation (Additional file 6: Figure S3), suggesting the requirement for TEX19 may have an upper threshold.
To determine whether TEX19 plays a role in self-renewal/proliferation in tumours in vivo we developed SW480 and HCT116 cell lines carrying an inducible shRNA cassette. A clone (TEX19shRNA-SW480-c3) was selected and proliferation analysis with and without doxycycline (dox) was carried out (expressing and not expressing TEX19shRNA). Induction of the shRNA resulted in a moderate, but statistically significant reduction in proliferation (Fig. 1c). A similar proliferative inhibition was observed with shRNA induction in HCT116 (Additional file 7: Figure S4). The inducible-shRNA SW480 cells were injected subcutaneously into NSG mice. One cohort was injected with dox, whereas a control population was not. Despite the relatively mild proliferative reduction observed in vitro, TEX19-shRNA induction in mice resulted in significant reduction of tumour volume, indicating that TEX19 expression is required for tumour development (Fig. 1d).
To gain insight into the role that TEX19 plays, we assessed various parameters of cells depleted for TEX19. Whilst proliferation of SW480 cells is inhibited following TEX19-depletion, the cells do not stain with trypan blue, suggesting that they retain viability, at least in the short-medium term. We next tested whether these cells become apoptotic. This was assessed by western blot analysis of cleaved caspase-3, a marker of the caspase-dependent apoptotic programme. No measurable level of cleaved caspase-3 was detected (Fig. 2a), consistent with murine Tex19.1 -/- ESCs . Taken together these two observations indicate that TEX19-depleted cells remain viable and, unlike murine Tex19.1 -/- spermatocytes, are not undergoing measurable programmed cell death [33, 34]. Next we tested siRNA treated cells from the ELDA with β-galactosidase, a measure of lysosome-dependent senescence. No measurable staining was observed, indicating these cells do not appear to be senescent (Fig. 2b). However, when TEX19-siRNA treated cells that failed to proliferate were washed and placed in siRNA-free fresh media, they did not re-initiate proliferation, suggesting that they have entered a non-senescent, non-apoptotic state from which they cannot readily recover, possibly a quiescent-like state.
To assess the cell cycle status of TEX19-depleted cells we analysed DNA content using FACS (Fig. 2c, d). The percentage of cells with a 2C compliment (G1) appears to remain unaltered. However, more cells accrue in S-phase and there are fewer cells with a full 4C compliment (G2) indicating that TEX19-depleted cells appear to have a delay in S-phase progression, albeit limited. We employed western blots on whole cell extracts of TEX19-depleted cells using antibodies to assess cell cycle progression [anti-phopho CDK2 Tyr15 (G1-S transition), anti-phopho histone H3 Ser10 (mitosis), anti-actin (loading control)] (Fig. 2e). There was no notable change in phospho-CDK2, supporting the FACS data, which indicate these cells progress normally into S-phase. There is an apparent reduction in the levels of phopho-histone H3 indicating there are fewer cells entering mitosis, again, consistent with the FACS profile which shows a limited delay in S-phase progression/completion. Collectively, these data indicate that whilst TEX19-depleted cells are viable (in the short-term, at least), the inhibition of proliferation might be linked to a delayed progression through S-phase which does not trigger apoptosis or senescence.
TEX19 is present is both the nucleus and the cytoplasm of human cancer cells
To gain insight into the possible function(s) of TEX19 in cancer cells, we assessed cellular localization. Previous studies on murine cells have reported a predominantly cytoplasmic localization for Tex19.1 [33, 34], but with some nuclear Tex19.1 in placental cells . Immunostaining of TEX19 in sub-confluent SW480 cells showed TEX19 located in both the cytoplasm and the nucleus, with some cells having a stronger nuclear staining than others (Fig. 3a). To further verify that there was a nuclear fraction of TEX19, we carried out western blots on nuclear and cytoplasmic extracts, which demonstrated that the majority of TEX19 is cytoplasmic in sub-confluent SW480 cells, but there is a measurable amount of TEX19 in the nucleus (Fig. 3b). To further verify the finding that some TEX19 is nuclear, we treated SW480 cells with leptomycin B (LMB), an inhibitor of the CRM1-dependent nuclear export pathway. LMB treated cells have a clear accumulation of TEX19 in the nucleus (Fig. 3c). Interestingly, the nuclear TEX19 in LMB treated cells forms clear foci, potentially indicating that TEX19 is forming region-specific complexes within the nucleus. These foci are consistent with chromatin association, so we isolated chromatin from sub-confluent SW480 cells and treated it with increasing concentrations of salt. TEX19 dissociated from the chromatin fraction at low salt concentrations indicating it does not have a strong association with chromatin (under these conditions; Fig. 3d). To determine whether nuclear localization of TEX19 is a common feature of cancer cells, we stained a second cell line, H460 (lung carcinoma). As for SW480 cells, sub-confluent H460 cells have nuclear and cytoplasmic TEX19 (Fig. 3e). We noticed, however, when cells were grown to over-confluence that TEX19 becomes excluded from the nucleus and appears to be solely cytoplasmic (Fig. 3e). To expand this observation, we grew colonospheres from SW480 cells, which are enriched for cancer stem-like cells , and assessed TEX19 localization. In these spheres, where cells are in close contact, TEX19 is predominantly cytoplasmic (Fig. 3f), consistent with the majority of Tex19.1 in murine tissue [33, 34]. Remarkably, in the germline tumour cell line, NTERA2, anti-TEX19 staining is predominantly nuclear (Fig. 3g), which could infer a link to germline/stem capabilities for TEX19.
TEX19 localization in human testis and cancer tissues
Our finding that human cancer cells have both nuclear/cytoplasmic TEX19, led us to investigate the localization in human cancerous tissues. Previous analysis of human TEX19 by immunohistochemistry (IHC) demonstrated that it is not present in normal healthy non-testis tissues, however, analysis of human testes lead to the proposal that TEX19 was located in seminiferous tubule Sertoli cells . This, seems to be in conflict with a direct role for TEX19 in germ cells / stem cells. To explore this further we used immunofluorescence to co-stain human testes with anti-TEX19 and anti-vimentin antibodies; (vimentin is a Sertoli cell marker). TEX19 staining is located to the basal layer, which mostly consists of spermatagonial cells and basal sections of Sertoli cells (Fig. 4a) , indicating that TEX19 staining is in specific cells or specific sub-cellular regions. Co-staining with an anti-vimentin antibody reveals that the high intensity TEX19 staining, whist in close proximity to the vimentin stain, does not directly co-localize (Fig. 4a), possibly indicating that TEX19 is present in a sub-compartment of Sertoli cells or in cells closely associated with Sertoli cells. There does, however, appear to be a low intensity TEX19 staining that that is quite extensive throughout the basal regions, including Sertoli cells, suggesting distinct TEX19 positive regions within the basal areas of seminiferous tubules. Whilst localization was mostly cytoplasmic, we observed foci within large nuclei of cells located within the basal layer of the tubules, possibly spermatagonia (Fig. 4b). Spermatagonia express MAGE genes (known CT genes), so we co-stained tubules with anti-MAGE-A1 antibodies. This appears to show TEX19 foci only within the nuclei of MAGE-A1 positive cells (Fig. 4c). This indicates that there are distinct cellular and sub-cellular TEX19 fractions within the testis, consistent with cancer cells.
We next determined the subcellular localization of TEX19 in cancerous tissue. We used colon cancer tissue and matched histologically non-cancerous adjacent tissue . Immunofluorescence revealed that adjacent, clear margin tissue with a morphologically normal appearance did not stain positive for TEX19 (Fig. 4d). The cancerous tissue, however, had regions of strong TEX19 staining (Fig. 4f) demonstrating that TEX19 encodes an antigen within colorectal cancer tissue. Cancerous tissue has heterogeneous regions that have high levels of TEX19 or none/low levels of TEX19, which fits with emerging models of tumour heterogeneity [49, 50]. The regions of intense TEX19 staining reveal that staining appears to be mostly cytoplasmic (Fig. 4f), consistent with highly confluent cancer cells and the majority of closely associated cells within colonospheres (Fig. 3). We cannot, however, exclude the possibility of low levels of nuclear TEX19 in these cells and we did observe occasional TEX19 foci associated with DAPI stained nuclear material in the tumour tissue (Fig. 4f).
TEX19 is associated with early adenoma stages of colorectal cancer development
To determine the stage of tumour progression at which TEX19 becomes apparent, we used IHC to stain colorectal cancer progression arrays (Fig. 5a). We analysed seven independent colorectal tumour progression arrays. TEX19 was present in all arrays with highest staining observed in the early adenomas (<2 cm), with different levels present in later stage disease tissues (Fig. 5b). This observation indicates that in colorectal cancer development TEX19 is present at an early stage in all array series tested, potentially suggesting a requirement for TEX19 at an early phase.
TEX19 regulates distinct transposable element transcripts in a cell-specific fashion
Previously, it has been demonstrated that murine Tex19.1 represses transcript levels from some endogenous retroviruses (e.g., MMERVK10C) during spermatogenesis, but not other TE transcripts (including LINEs, SINEs and other endogenous retro elements), suggesting that it can differentially regulate TE transcript levels. In contrast, in Tex19.1 -/- murine placental tissue, where Tex19.1 regulates intra-uterine growth, distinct TEs, such as LINEs are up-regulated, whereas expression of the endogenous retrovirus MMERVK10C, which is repressed by Tex19.1 during spermatogenesis, remains unaltered [34, 35]. Murine Tex19.1 -/- ESCs exhibit yet another pattern of TE expression, with up-regulation of MMERVK10C and other TEs, such as LINE-1 . These findings indicate that whilst Tex19.1 regulates TE transcript levels in the mouse, there is heterogeneity that might reflect a tissue or cell type distinction in Tex19.1 function.
TE activation occurs during oncogenesis [51, 52]. Given that human TEX19 might regulate progression through S-phase (see above), and the role for murine Tex19.1 in TE control, it is not unreasonable to postulate that elevated transposition or TE expression caused by depletion of TEX19 might retard S-phase. Given this, we used RT-qPCR to determine whether depletion of TEX19 resulted in alteration in TE RNA levels in SW480 cells. As for murine spermatogenesis, we found no change in LINE or SINE transcript levels. We did, however, find that some HERVK transcripts were altered; unexpectedly, some were down-regulated (e.g., HERVK pro), but HERVK HML2 rec was up-regulated (Fig. 6a). This demonstrates that human TEX19 differentially controls HERVK transcripts in SW480 cells. The reduction in some transcripts was a little unexpected as murine Tex19.1 appears to function in TE transcript suppression . Given that we saw reductions in transcripts, and given the fact that murine Tex19.1 also controls expression of protein encoding genes in the placenta, we questioned whether reduction of human TEX19 might activate the human PIWI pathway, which may then reduce some HERVK transcripts. To assess this, we determined expression levels of human PIWI orthologues (PIWIL1-4). All four were expressed in SW480 cells and PIWIL1-3 are up-regulated following TEX19 depletion (Fig. 6b; PIWIL4 was not).
To test whether PIWI pathway activation could reduce levels of some HERVK transcripts, we carried out single and double gene siRNA depletion of TEX19 and PIWIL1 in SW480 cells. Depletion of PIWIL1 alone results in both an elevation and a reduction of HERVK transcripts (Fig. 6c), indicating a differential suppression and activation role for PIWIL1. Remarkably, co-depletion of PIWIL1 and TEX19 results in no measurable change to HERVK transcript levels, suggesting that the HERVK transcript level changes following depletion of TEX19 in SW480 cells could be PIWIL1-dependent (Fig. 6d). However, if this was simply due to PIWIL1 acting downstream of TEX19, co-depletion of TEX19 and PIWIL1 should result in a PIWIL1-difficient phenotype (e.g., elevation of HERVK pro transcripts), which is not the case. Alternatively, this points to a more complex interplay between TEX19 and PIWIL1 in SW480 cancer cells, possibly indicating that TEX19 and PIWIL1 have opposing and independent roles in regulating TE transcripts (for example, TEX19 positively regulates HERVK pro, whereas PIWIL1 negatively regulates HERVK pro transcripts). This model is supported by the observation that HERVK gag transcripts (for example) are reduced following TEX19 depletion in H460 cells, which do not exhibit measurable expression of PIWIL1 (Fig. 6d). A model in which TEX19 functions independently of PIWI pathway proteins is consistent with observations in the mouse .
To assess the universality of this phenomenon, we explored PIWIL1 expression in other cell lines (Fig. 6e). We could detect no expression in A2780, H460, HCT116 or HeLaS3 cells and virtually no expression in PEO14. In two of the negative lines, H460 and A2780, we analysed the expression of the other PIWI paralogues. We could detect no expression of paralogues in H460, with A2780 expressing PIWIL2 and relatively low levels of PIWIL4; however, the levels of neither were significantly altered by TEX19 depletion, suggesting that TEX19 regulation of PIWI gene expression may not be universal in all cancer cell types (Fig. 6b).
We next addressed whether TEX19 influenced transcriptional activation of HERV genes in other cell lines, including H460 where no PIWI paralogues were expressed. These analyses indicate that there are some changes (for example, see Fig. 6f, g). For example, A2780 shows considerable activation of HERVK gag transcripts in response to a relatively modest depletion of TEX19 (Fig. 6f).
TEX19 regulates protein coding gene transcript levels
To explore the possibility that TEX19 acts as a protein coding gene transcriptional regulator in cancer cells, we carried out RNA sequencing on total polyA-RNA extracted from untreated SW480 cells and cells treated with a TEX19 siRNA. Transcript levels from 80 genes were found to be significantly (P < 0.05) altered (up-/down-regulated), including a reduction in TEX19 mRNA, as expected, and an increase in PIWIL1 mRNA, consistent with our RT-qPCR (Additional file 8; Figure S5). Of the 80 genes, some are known CT genes; for example, we previously reported SEPT12 and RAD21L1 as CT genes , so these genes require TEX19 to control their expression in SW480 cells. Given that we found that PIWIL1 expression regulation is not uniform in all cell lines, we carried out RT-qPCR for 52 of these genes (those with an RNA-seq P value of <0.01; Additional file 3; Table S3) in additional cell lines (H460, A2780, PEO14, NTERA2, and an independent duplicate analysis of SW480). No genes exhibited consistent changes across all cells lines (Additional file 3; Table S3), and distinct analysis of SW480 gave some inconsistencies suggesting a variability due to TEX19 dose (independent siRNA depletion of TEX19 is unlikely to have been uniform in all experiments). However, many gene transcripts did exhibit changes (up or down) indicating that TEX19 can regulate transcript levels of protein coding genes, possibly in a TEX19 dose-dependent fashion. Some of the genes, for example, TSN and MYB, are potential regulators of proliferation [53,54,55,56,57] and so this could indicate that TEX19 is required by cancer cells to drive proliferation by maintaining sufficient levels of oncogenic transcripts.
High TEX19 expression is a prognostic marker in a range of cancer types
Expression of germline genes has previously been reported to be linked to poor prognosis in cancers, for example, lung cancer (for example, see ). Given the finding that TEX19 controls cancer cell proliferation we wished to explore whether TEX19 expression influences clinical progression. We used RNA-seq data from TCGA to determine whether high levels of TEX19 expression were linked to poor prognosis. For each cohort of cancer patients we divided the population into high and low TEX19 expression groups split by the median value and performed survival analysis. 37 data sets for distinct cancer groups were available, of which 27 held sufficient data for analysis (TCGA; Additional file 9; Table S4). High TEX19 expression (as split by the median) is significantly linked to overall survival in seven data sets. For breast invasive carcinoma (BRCA; Fig. 7a), prostate adenocarcinoma (PRAD; Fig. 7b) and the pan-kidney cohort (KIPAN; Fig. 7c) high TEX19 expression is associated with poor prognosis; although the difference is marginal for PRAD. The KIPAN data set consists of data from three distinct renal cancer data sets (kidney chromophobe – KICH, kidney renal clear cell carcinoma – KIRC, kidney renal cell carcinoma – KIRP). Analysis of two independent kidney cancer data sets (KIRK and KIRP) reveals that both show significant reductions of overall survival for the higher TEX19 expression cohort of patients (Additional file 10: Figure S6a/b); KICH is a rare renal cancer, only contributing to approximately 5% of all renal cancers , and it has a better prognosis than more common forms of renal cancer , so limited data excluded it from individual analysis.
Intriguingly, higher TEX19 expression is linked to a better prognosis for gliomas (GBMLGG; Fig. 7d) and brain lower grade glioma (LGG; Additional file 10: Figure S6c). This finding was unexpected as previous studies have indicated germ line gene expression is linked to a poor prognosis.
The use of a single criteria for the cohort split point, such as splitting by the median, limits analyses of this nature. Use of other split points resulted in additional cancer types showing TEX19 expression linked to prognosis; two examples are the data sets for lung adenocarcinoma (LUAD) and cervical squamous cell carcinoma/endocervical adenocarcinoma (CESC) when patients are split into the upper 25% of TEX19 expression vs. the lower 75% expression for cancers where clinical data are available, where a significant (P = 0.039 and P = 0.038 respectively) link to poor prognosis is observed [which is not significant (P = 0.136 and P = 0.236 respectively) when the split is by the standard method of the median] (Additional file 11; Figure S7). Increased data volume and further sub-categorization of tumour types is likely to further resolve which cancer types can be stratified by TEX19 expression profiling, but these initial findings clearly indicate that TEX19 expression is linked to distinct clinical outcomes. In many of the cell line experiments we conducted we used colon cancer cells, yet interestingly, none of the splits we allocated to colorectal cancer data (263 patients; 124 expressing TEX19 at the threshold set for positive expression) indicated a link to prognosis. There could be number of reasons for this, not least of which is the heterogeneous nature of TEX19 distribution to distinct tumour regions in the colon tumour samples we analysed (i.e. the RNA-seq data may have been obtained from tumour biopsy regions that may have had limited/no TEX19 expression); given this, we cannot rule out a link between TEX19 expression and cancer progression for colorectal cancers. The distinct link of high TEX19 expression to positive and negative prognosis is discussed further below.
The idea that cancer cells achieve self-renewal potential by re-activating programmes that regulate the germ/stem like state, and undergo a soma-to-germline transition is gaining traction (for example, see [2, 3, 5]). Germline functions are known to contribute to distinct biological features of cancers [11,12,13], including invasiveness/metastasis (for example, [21,22,23, 25]) and maintenance of proliferative potential (for example, [14,15,16,17,18,19]). Some activities are linked to poor outcomes; for example, elevated expression of SPANX-A/C/D is linked to poor prognosis in breast cancers . Furthermore, germline gene expression in lung cancer has been linked with aggressive, metastases prone disease and can be used for stratification of patients to identify cohorts who might benefit from targeted therapies . Even meiotic chromosome regulators have been shown to contribute to oncogenesis by driving inter chromosomal associations required for oncogenic alternative lengthening of telomeres . So, germline/stem cell factors can make distinct contributions to cancer progression, maintenance and evolution.
TEX19 as an oncogenic driver
Despite the growing evidence for the soma-to-germline transition of tumours, the reported roles of specific germline genes in cancers remains limited. Here we find that TEX19 expression is required to maintain the proliferative potential of a range of different cancer cells. Given that TEX19 is expressed in many cancer types, this might infer that it is an oncogenic factor, indeed, all cell lines / tumour samples we analysed showed evidence of TEX19 expression. This is not the case for all database studies [for example, the Human Protein Atlas (www.proteinatlas.org) reports only limited TEX19 expression], but we have demonstrated that some areas of later stage tumours are more prone to TEX19 expression, suggesting that expression can be regional within an advanced tumour. It is known that tumours can evolve and acquire a high degree of intra- and inter-tumour heterogeneity, and so database samples may also include information acquired from tumour regions that do not express TEX19 [49, 50]. The heterogeneous distribution of TEX19 indicates two possibilities; firstly, TEX19 may be ‘on’ during the early stages of tumourigenesis and becomes deactivated during the evolution of the tumour, or, alternatively, TEX19 only becomes activated in specific regions as the tumour develops and grows. The finding that germline genes are actually required for the early oncogenic process in D. melanogaster l(3)mbt tumours might suggest the former is the case . Our analysis of colorectal tumour progression profiles (Fig. 5) supports this view, as TEX19 was detected in all early adenomas, but was not detected in some samples of later stages of tumour progression which could point to an early ‘on’ later ‘off’ model for TEX19. This suggests that therapeutic targeting of TEX19 might not eliminate all tumour cells in later stage tumours. However, given the fact that TEX19 function is implicated in stemness , it might be the case that the TEX19 positive cells are those that retain stem-like features and thus therapeutic targeting of these cells remains important, as these cells might be driving the poor prognosis/therapeutic resistance .
How does TEX19 modulate proliferation?
We have demonstrated that TEX19 expression is required to maintain proliferation/self-renewal in a range of cancer cell types. Loss of murine Tex19.1 can result in spermatogenic cells entering apoptosis, however, analysis of TEX19-depleted human cancer cells indicates that they are likely to be in a quiescent-like state, which appears to be linked to a failure to proceed through S-phase with normal kinetics. This observation is in contrast to murine Tex19.1 -/- ESCs, which, whilst being defective in self-renewal, do not exhibit any overt S-phase defects . Murine Tex19.1 has been shown to control levels of TE transcripts and, in the case of the female placenta, other protein coding transcripts . We have demonstrated here that TEX19 in SW480 cells can influence TE transcript levels. In SW480 cells this appears to be counteracted by a PIWIL1-dependent mechanism. A model in which TEX19 and PIWIL1 serve in opposing and independent mechanisms for TE transcript control is consistent with murine Tex19.1 acting on TEs in a PIWI-independent fashion . Indeed, in other cancer cells lines we tested PIWIL1 is not expressed and yet TE transcripts exhibit a measurable change upon TEX19 depletion, which supports a TEX19-dependent, PIWI-independent pathway.
The ovarian carcinoma cell line A2780 showed considerable activation of HERVK gag transcript levels upon a relatively moderate reduction of TEX19. A2780 cells do not express measurable levels of PIWIL1 and the PIWI orthologues that are expressed are not altered upon TEX19 depletion. This indicates that in A2780 cells TEX19 appears to operate in a PIWI-independent mechanism for TE suppression, similar to that proposed for murine placental TE regulation . These findings also demonstrated that TEX19 can act in a repressive and activating fashion for some TE transcripts in a cell- and/or dose-dependent fashion.
Given this, we explored protein coding gene changes with an aim of identifying changes common to all cells. This showed that no gene transcripts were consistently altered upon TEX19 depletion. However, coding gene transcripts were altered (up and down) indicating that TEX19 could regulate the transcripts/transcription of a cohort of oncogenic protein coding genes to foster a proliferative state, possibly in a dose-dependent fashion.
SSX2, another CTA, is a chromatin regulator  and it has been inferred that it may regulate cancer cell proliferation through transcriptional regulation . Also, the germline-specific chromatin regulator ATAD2 drives various cancer progression phenotypes via transcriptional regulation and is linked to poor prognoses in various cancers and offers an important potential therapeutic target [62,63,64,65,66,67,68,69,70,71,72]. These findings indicate there are CTAs that can directly modulate transcription, and we postulate that TEX19 could function in a similar fashion controlling cellular transcript levels, either at the transcriptional and/or post-transcriptional levels. As for mouse Tex19.1, TEX19 in cancer cells can operate on a small sub-set of protein coding and/or TE transcripts, although the latter may be indirect.
TEX19 is both cytoplasmic and nuclear in cancer cells and testis cells
Consistent with a direct role in transcriptional regulation, we demonstrate that human TEX19 can locate to the nucleus, although there is no apparent nuclear localization/export signals on TEX19, which might suggest nuclear localization in response to cellular status is regulated by interacting partners. Murine Tex19.1 interacts with the E3 ubiquitin ligase Ubr2 which contains a nuclear localization signal, so a role for a UBR2-TEX19 interaction in human cancers would be worthy of further investigation . TEX19 nuclear localisation appears to be linked to cell density and may be related to proliferative state, with nuclear TEX19 being associated with proliferation. Whilst murine Tex19.1 is predominantly localized to the cytoplasm, nuclear Tex19.1 can be observed in placental tissues indicating commonalities between murine and human proteins [33, 34]. Additionally, we note nuclear foci of TEX19 in testis, germ cell tumour line NTERA2 and LMB treated nuclei; the functional relevance, if any, is unknown although it is a noteworthy observation.
Recently, immunohistochemistry studies indicated that human TEX19 was localized to Sertoli cells . Our immunofluorescence analysis of co-staining with the Sertoli cell marker vimentin did not show direct co-localisation of the high intensity TEX19 staining regions (although there appears to be a low intensity TEX19 staining throughout the basal region, including Sertoli cells), rather a close association, suggesting that TEX19 may not be exclusively Sertoli cell specific. Furthermore, IHC staining of normal testis appears to show nuclear localization/speckling in some of the large nuclei , consistent with our observation. Zhong and co-workers  extended their analysis to demonstrate that TEX19 was present in bladder cancer samples. Whilst most of the TEX19 they observed in these samples appeared to be cytoplasmic, there are clearly cells within the tumours that exhibit some nuclear staining with the anti-TEX19 antibodies employed .
TEX19 expression influences clinical outcomes
That TEX19 expression helps drive proliferative potential of cancer cells suggests that it might influence disease progression / outcome in patients. Our analysis of overall survival indicates that for a number of cancers, including breast cancer and renal cancers, that there is a significant correlation between higher TEX19 expression and poor prognosis, supporting a potential functional association. These analyses might be an underestimation of the influence of TEX19 expression as our analysis was based on splitting cancer patient cohorts based on median TEX19 expression. Use of the median split means that the two populations being compared both have high numbers of TEX19 expressing cancers; if TEX19 expression alone (irrespective of the levels) is sufficient to drive cancers, then in many of our analyses a split based on the median would not detect a correlative link between TEX19 expression and a poor prognosis. Ideally, we would have split all cohorts into those expressing TEX19 and those not. This approach, however, was untenable as many data sets had an imbalance of negative vs. positive TEX19 expressing cancers, negating statistical analysis. Moreover, this is further complicated by the difficulties of ascribing tumour biopsies as having no expression given the sensitivity/depth of modern deep RNA sequencing technologies, which can identify low abundance transcripts for almost all annotated genes . Despite these limitations, the analysis of breast cancers and renal cancers clearly indicate a correlative link between high TEX19 expression and poor prognosis, consistent with a functional role for TEX19 as an oncogenic proliferative driver.
Surprisingly, we observed the converse relationship for gliomas where higher TEX19 expression is linked to a better prognosis, suggesting it has favorable activity in neuronal cells. This inverse influence on disease outcome has also been observed for T-box transcription factors, which both positively/negatively regulate gene expression during embryonic development . For example, as for TEX19, TBX3 appears to have tumour suppressing activity in glioblastomas  but oncogenic activity in a number of solid tumours (for examples, see [77,78,79]; for review, see ). This commonality between T-box transcription factors and TEX19 could infer a functional link in the distinct regulation of developmental/proliferative genes in distinct cancer types. The factors that set neuronal tumours apart from other tumour types are likely to be multifold, however, it is noteworthy that LINE-1 retrotransposition is active in somatic neuronal cells ; it is not unreasonable to postulate that TEX19 production in neuronal malignancies could limit LINE-1 transposition events and thus limit the evolutionary capacity of the diseased genome and therefore the aggressiveness of the tumour.
Here we have identified human TEX19 as a driver of cancer cell proliferative potential. Importantly, we demonstrate that depletion of TEX19 may result in S-phase defects, however, the exact functional role of TEX19 remains unclear. Evidence is starting to emerge to indicate that TEX19 is a transcriptional/transcript regulator that has a degree of plasticity, which may be modulated dependent upon the cell/tissue requirements. Whatever the exact role, it is clear that TEX19 expression influences cancer prognosis and should be considered as a highly specific target for the development of novel anti-cancer therapeutic agents.
American type culture collection
European Collection of Authenticated Cell Cultures
Extreme limiting dilution assay
Embryonic stem cell
Fetal bovine serum
Human endogenous retro virus
Long terminal repeat
The Cancer Genome Atlas
Nassar D, Blanpain C. Cancer stem cells: basic concepts and therapeutic implications. Annu Rev Pathol. 2016;11:47–76.
McFarlane RJ, Feichtinger J, Larcombe L. Cancer germline gene activation: friend or foe? Cell Cycle. 2014;13:2151–2.
Feichtinger J, Larcombe L, McFarlane RJ. Meta-analysis of expression of l(3)mbt tumor-associated germline genes supports the model that a soma-to-germline transition is a hallmark of human cancers. Int J Cancer. 2014;134:2359–65.
Koslowski M, Bell C, Seitz G, Lehr HA, Roemer K, Müntefering H, Huber C, Sahin U, Türeci O. Frequent nonrandom activation of germ-line genes in human cancer. Cancer Res. 2004;64:5988–93.
McFarlane RJ, Feichtinger J, Larcombe L. Germline/meiotic genes in cancer: new dimensions. Cell Cycle. 2015;14:791–2.
Nielsen AY, Gjerstorff MF. Ectopic expression of testis germ cell proteins in cancer and its potential role in genomic instability. Int J Mol Sci. 2016;17(6). doi:10.3390/ijms17060890.
Janic A, Mendizabal L, Llamazares S, Rossell D, Gonzalez C. Ectopic expression of germline genes drives malignant brain tumor growth in Drosophila. Science. 2010;330:1824–7.
Fagegaltier D, Falciatori I, Czech B, Castel S, Perrimon N, Simcox A, Hannon GJ. Oncogenic transformation of Drosophila somatic cells induces a functional piRNA pathway. Genes Dev. 2016;30:1623–35.
Sumiyoshi T, Sato K, Yamamoto H, Iwasaki YW, Siomi H, Siomi MC. Loss of l(3)mbt leads to acquisition of the pin-pong cycle in Drosophila ovarian somatic cells. Genes Dev. 2016;30:1617–22.
Simpson AJ, Caballero OL, Jungbluth A, Chen YT, Old LJ. Cancer/testis antigens, gametogenesis and cancer. Nat Rev Cancer. 2005;5:615–25.
Fratta E, Coral S, Covre A, Parisi G, Colizzi F, Danielli R, Nicolay HJ, Sigalotti L, Maio M. The biology of cancer testis antigens: putative function, regulation and therapeutic potential. Mol Oncol. 2011;5:164–82.
Whitehurst AW. Cause and consequence of cancer/testis antigen activation in cancer. Annu Rev Pharmacol Toxicol. 2014;54:251–71.
Gjerstorff MF, Andersen MH, Ditzel HJ. Oncogenic cancer/testis antigens: prime candidates for immunotherapy. Oncotarget. 2015;6:15772–87.
Por E, Byun HJ, Lee EJ, Lim JH, Jung SY, Park I, Kim YM, Jeoung DI, Lee H. The cancer/testis antigen CAGE with oncogenic potential stimulates cell proliferation by up-regulating cyclins D1 and E in an AP-1- and E2F-dependent manner. J Biol Chem. 2010;285:14475–85.
Whitehurst AW, Xie Y, Purinton SC, Cappell KM, Swanik JT, Larson B, Girard L, Schorge JO, White MA. Tumor antigen acrosin binding protein normalizes mitotic spindle function to promote cancer cell proliferation. Cancer Res. 2010;70:7652–61.
Cappell KM, Sinnot R, Taus P, Maxfield K, Scarbrough M, Whitehurst AW. Multiple cancer testis antigens function to support tumor cell mitotic fidelity. Mol Cell Biol. 2012;32:4131–40.
D’Arcy P, Maruwge W, Wolaham B, Ma L, Brodin B. Oncogenic functions of the cancer-testis antigen SSX on the proliferation, survival, and signaling pathways of cancer cells. PLoS One. 2014;9:e95136.
Maxfield KE, Taus PJ, Corcoran K, Wooten J, Macion J, Shou Y, Borromeo M, Kollipara RK, Yan J, Xie Y, Xie XJ, Whitehurst AW. Comprehensive functional characterization of cancer-testis antigens defines obligate participation in multiple hallmarks of cancer. Nat Commun. 2015;16:8840.
Greve KB, Lindgreen JN, Terp MG, Pedersen CB, Schmidt S, Mollenhauer J, Kristensen SB, Andersen RS, Relster MM, Ditzel HJ, Gjerstorff MF. Ectopic expression of cancer/testis antigen SSX2 induces DNA damage and promotes genomic instability. Mol Oncol. 2015;9:437–49.
Wang D, Wang J, Ding N, Li Y, Yang Y, Fang X, Zhao H. MAGE-A1 promotes melanoma proliferation and migration through c-JUN activation. Biochem Biophys Res Comm. 2016;473:959–65.
Caballero OL, Cohen T, Gurung S, Chua R, Lee P, Chen YT, Jat P, Simpson AJ. Effects of CT-Xp gene knock down in melanoma cell lines. Oncotarget. 2013;4:531–41.
Yang F, Zhou X, Miao X, Zhang T, Hang X, Tie R, Liu N, Tian F, Wang F, Yuan J. MAGEC2, an epithelial-mesenchymal transition inducer, is associated with breast cancer metastasis. Breast Cancer Res Treat. 2014;145:23–32.
Shang B, Gao A, Pan Y, Zhang G, Tu J, Zhou Y, Yang P, Cao Z, Wei Q, Ding Y, Zhang J, Zhao Y, Zhou Q. CT45A1 acts as a new proto-oncogene to trigger tumorigenesis and cancer metastasis. Cell Death Dis. 2014;5:e1285.
Hsiao YJ, Su KY, Hsu YC, Chang GC, Chen JS, Chen HY, Hong QS, Hsu SC, Kang PH, Hsu CY, Ho BC, Yang TH, Wang CY, Jou YS, Yang PC, Yu SL. SPANXA suppresses EMT by inhibiting c-JUN/SNAI2 signaling in lung adenocarcinoma. Oncotarget. 2016;doi:10.18632/Oncotarget.10088.
Maine EA, Westcott JM, Prechtl AM, Dang TT, Whitehurst AW, Pearson GW. The cancer-testis antigens SPANX-A/C/D and CTAG2 promote breast cancer invasion. Oncotarget. 2016;7:14708–26.
Feichtinger J, Aldeailej I, Anderson R, Almutairi M, Almatrafi A, Alsiwiehri N, Griffiths K, Stuart N, Wakeman JA, Larcombe L, McFarlane RJ. Meta-analysis of clinical data using human meiotic genes identifies a novel cohort of highly restricted cancer-specific marker genes. Oncotarget. 2012;3:843–53.
Sammut SJ, Feichtinger J, Stuart N, Wakeman JA, Larcombe L, McFarlane RJ. A novel cohort of cancer-testis biomarker genes revealed through meta-analysis of clinical data sets. Oncoscience. 2014;1:349–59.
Wang PJ, McCarrey JR, Yang F, Page DC. An abundance of X-linked genes expressed in spermatagonia. Nat Genet. 2001;27:422–6.
Kuntz S, Kieffer E, Bianchetti L, Lamoureux N, Fuhrmann G, Viville S. Tex19, a mammalian-specific protein with a restricted expression in pluripotent stem cells and germ line. Stem Cells. 2008;26:734–44.
Wang C, Gu Y, Zhang K, Xie K, Zhu M, Dai N, Jiang Y, Guo X, Liu M, Dai J, Wu L, Jin G, Ma H, Jiang T, Yin R, Xia Y, Liu L, Wang S, Shen B, Huo R, et al. Systematic identification of genes with a cancer-testis expression pattern in 19 cancer types. Nature Comm. 2015;7:10499.
Zhong J, Chen Y, Liao X, Li J, Wang H, Wu C, Zou X, Yang G, Shi J, Luo L, Liu L, Deng J, Tang A. Testis expressed 19 is a novel cancer-testis antigen expressed in bladder cancer. Tumour Biol. 2016;37:7757–65.
Hackett JA, Reddington JP, Nestor CE, Dunican DS, Branco MR, Reichmann J, Reik W, Surani MA, Adams IR, Meehan RR. Promoter DNA methylation couples genome-defense mechanisms to epigenetic reprogramming in the mouse germline. Development. 2012;139:3623–32.
Tarabay Y, Kieffer E, Teletin M, Celebi C, Van Montfoort A, Zamudio N, Achour M, Ramy EI, Gazdag E, Tropel P, Mark M, Bourc’his D, Ville S. The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported development. Human Rep. 2013;28:2201–14.
Öllinger R, Childs AJ, Burgess HM, Speed RM, Lundergaard PR, Reynolds N, Gray NK, Cooke HJ, Adams IR. Deletion of the pluripotency-associated Tex19.1 gene causes activation of endogenous retroviruses and defective spermatogenesis in mice. PLoS Genet. 2008;4:e1000199.
Reichmann J, Reddington JP, Best D, Read D, Öllinger R, Meehan RR, Adams IR. The genome-defense gene Tex19.1 suppresses LINE-1 retrotransposons in the placenta and prevents intra-uterine growth retardation in mice. Hum Mol Genet. 2013;22:1791–806.
Rousseaux S, Debernardi A, Jacquiau B, Vitte AL, Vesin A, Nagy-Mignotte H, Moro-Sibilot D, Brichon PY, Lantuejoul S, Hainaut P, Laffaire J, de Reyniés A, Beer DG, Timsit JF, Brambilla C, Brambilla E, Knochbin S. Ectopic activation of germline and placental genes identifies aggressive metastasis-prone lung cancers. Sci Trans Med. 2013;5:186ra66.
Hu Y, Smyth GK. ELDA: extreme limiting dilution analysis for comparing depleted and enriched populations in stem cell and other assays. J Immunol Methods. 2009;347:70–8.
Jezkova J, Williams JS, Jones-Hutchinson F, Sammut SJ, Gollins S, Cree I, Coupland S, McFarlane RJ, Wakeman JA. Brachyury regulates proliferation of cancer cells via a p27Kip1-dependent pathway. Oncotarget. 2014;5:3813–22.
Kim D, Pertea G, Trapnell C, Pimentel H, Kelley R, Salzberg SL. TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biol. 2013;14:R4.
Anders S, Pyl PT, Huber W. HTSeq – a Python framework to work with high-throughput sequence data. Bioinformatics. 2014;31:166–9.
Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014;15:550.
Benjamini Y, Hochberg Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Ser B Methodol. 1995;57:289–300.
Falcon S, Gentleman R. Using GOstats to test gene lists for GO term association. Bioinformatics. 2007;23:257–8.
Law CW, Chen Y, Shi W, Smyth GK. Voom: precision weights unlock linear model analysis tools for RNA-seq read counts. Genome Biol. 2014;15:R29.
Smyth GK. Limma: linear models for microarray data. In: Gentleman R, Huber W, Irizarry R, Dudoit S, editors. Bioinformatics and Computational Biology Solutions Using R and Bioconductor. New York: Springer; 2005. p. 397–420.
Therneau TM, Grambsch PM. Modelling survival data: extending the Cox model. New York: Springer; 2000.
Neto FT, Bach PV, Najari BB, Li PS, Goldstein M. Spermatogenesis in humans and its affecting factors. Semin Cell Dev Biol. 2016;59:10–26.
Jezkova J, Williams JS, Pinto F, Sammut SJ, Williams GT, Gollins S, McFarlane RJ, Reis RM, Wakeman JA. Brachyury identifies a class of enteroendocrine cells in normal human intestinal crypts and colorectal cancer. Oncotarget. 2016;7:11478–86.
Burrell RA, McGranahan N, Bartek J, Swanton C. The causes and consequences of genetic heterogeneity in cancer evolution. Nature. 2013;501:338–45.
Meacham CE, Morrison SJ. Tumour heterogeneity and cancer cell plasticity. Nature. 2013;501:328–37.
Goodier JL. Retrotransposition in tumors and brains. Mob DNA. 2014;5:11.
Chenias B. Transposable elements in cancer and other human diseases. Curr Cancer Drug Targets. 2015;15:227–42.
Jaendling A, McFarlane RJ. Biological roles of translin and translin-associated factor X: RNA metabolism comes to the fore. Biochem J. 2010;429:225–34.
Gomez-Escobar N, Almobadel N, Alzahrani O, Feichtinger J, Planells-Palop V, Alshehri Z, Thallinger GG, Wakeman JA, McFarlane RJ. Translin and Trax differentially regulate telomere-associated transcript homeostasis. Oncotarget. 2016; doi:10.18632/Oncotarget.9278.
Ishida R, Ohado H, Sato H, Shionoiri C, Aoki K, Kasai M. A role for the octomeric ring protein, Translin, in mitotic cell division. FEBS Lett. 2002;525:105–10.
Yang S, Cho YS, Chennathukuzhi VM, Underkoffler LA, Loomes K, Hecht NB. Translin-associated factor-X is post-transcriptionally regulated by its partner protein TB-RBP, and both are essential for normal cell proliferation. J Biol Chem. 2004;279:12605–14.
George OL, Ness SA. Situational awareness: regulation of the myb transcription factor in differentiation, the cell cycle and oncogenesis. Cancers. 2014;6:2049–71.
Vera-Badillo FE, Conde E, Duran I. Chromophobe renal cell carcinoma: a review of an uncommon entity. Int J Urol. 2012;19:894–900.
Patard JJ, Leray E, Rioux-Leclercq N, Cindolo L, Ficarra V, Zisman A, De La Taille A, Tostain J, Artibani W, Abbou CC, Lobel B, Guillé F, Chopin DK, Mulders PF, Wood CG, Swanson DA, Fiqlin RA, Belldegrun AS, Pantuck AJ. Prognostic value of histologic subtypes in renal cell carcinoma: a multicenter experience. J Clin Oncol. 2005;23:2763–71.
Cho NW, Dilley RL, Lampson MA, Greenberg RA. Interchromosomal homology searches drive directional ALT telomere movement and synapsis. Cell. 2014;159:108–21.
Gjerstorff MF, Relster MM, Greve KB, Moeller JB, Elias D, Lindgreen JN, Schmidt S, Mollenhauer J, Voldborg B, Pedersen CB, Brückmann NH, Møllegaard NE, Ditzel HJ. SSX2 is a novel DNA-binding protein that antagonizes polycomb group body formation and gene repression. Nucleic Acids Res. 2014;42:11433–46.
Ciró M, Prosperini E, Quarto M, Grazini U, Walfridsson J, McBlane F, Nucifero P, Pacchiana G, Capara M, Christensen J, Helin K. ATAD2 is a novel cofactor for MYC, overexpressed and amplified in aggressive tumors. Cancer Res. 2009;69:8491–8.
Caron C, Lestrat C, Marsal S, Escoffier E, Curtet S, Virolle V, Barbry P, Debernardi A, Bramilla C, Bramilla E, Rousseaux S, Knochbin S. Functional characterization of ATAD2 as a new cancer/testis factor and predictor of poor prognosis in breast and lung cancers. Oncogene. 2010;29:5171–81.
Kalashnikova EV, Revenko AS, Gemo AT, Andrews NP, Tepper CG, Zou JX, Cardiff RD, Borowsky AD, Chen HW. ANCCA/ATAD2 overexpression identifies breast cancer patients with poor prognosis, acting to drive proliferation and survival of triple-negative cells through control of B-Myb and EZH2. Cancer Res. 2010;70:9402–12.
Boussouar F, Jamshidikia M, Morozumi Y, Rousseaux S, Khochbin S. Malignant genome reprogramming by ATAD2. Biochim Biophys Acta. 1829;2013:1010–4.
Hwang HW, Ha SY, Bang H, Park CK. ATAD2 as a poor prognostic marker for hepatocellular carcinoma after curative resection. Cancer Res. 2015;47:853–61.
Krakstad C, Tangen IL, Hoivik EA, Halle MK, Berg A, Werner HM, Raeder MB, Kusonmano K, Zou JX, Øyan AM, Stefansson I, Trovik J, Kalland KH, Chen HW, Salvesen HB. ATAD2 overexpression links to enrichment of B-MYB-translational signatures and development of aggressive endometrial carcinoma. Oncotarget. 2015;6:28440–52.
Lu WJ, Chua MS, So SK. Suppression of ATAD2 inhibits hepatocellular carcinoma progression through activity of p53- and p38-mediated apoptotic signaling. Oncotarget. 2015;6:41722–35.
Luo Y, Ye GY, Qin SL, Yu MH, Mu YF, Zhong M. ATAD2 overexpression identifies colorectal cancer patients with poor prognosis and drives proliferation of cancer cells. Gastroenterol Res Pract. 2015;2015:936564.
Zhang MJ, Zhang CZ, Du WJ, Yang XZ, Chen ZP. ATAD2 is overexpressed in gastric cancer and serves as an independent poor prognostic biomarker. Clin Transl Oncol. 2015;18:776–81.
Zheng L, Li T, Zhang Y, Guo Y, Yao J, Dou L, Guo K. Oncogene ATAD2 promotes cell proliferation, invasion and migration in cervical cancer. Oncol Rep. 2015;33:2337–44.
Hou M, Huang R, Song Y, Feng D, Jiang Y, Liu M. ATAD2 overexpression is associated with progression and prognosis in colorectal cancer. Jpn J Clin Oncol. 2016;46:222–7.
Yang F, Cheng Y, An JY, Kwon YT, Eckardt S, Leu NA, McLaughlin KJ, Wang PJ. The ubiquitin ligase Ubr2, a recognition E3 component of the N-end rule pathway, stabilizes Tex19.1 during spermatogenesis. PLoS One. 2010;5:e14017.
Hart T, Komori HK, LaMere S, Podshivalova K, Salomon DR. Finding the active genes in deep RNA-seq gene expression studies. BMC Genomics. 2013;14:778.
Wansleben S, Peres J, Hare S, Goding CR, Prince S. T-box transcription factors in cancer biology. Biochim Biophys Acta. 1846;2014:380–91.
Etcheverry A, Aubry M, de Tayrac M, Vauleon E, Boniface R, Guenot F, Saikali S, Hamlat A, Riffaud L, Menei P, Quillien V, Mosser J. DNA methylation in glioblastoma: impact on gene expression and clinical outcome. BMC Genomics. 2010;11:701.
Park JC, Chae YK, Son CH, Kim MS, Lee J, Ostrow K, Sidransky D, Hoque MO, Moon C. Epigenetic silencing of human T (brachyury homologue) gene in non-small-cell lung cancer. Biochem Biophys Res Commun. 2008;365:221–6.
Rodriguez M, Aladowicz E, Lanfrancone L, Goding CR. Tbx3 represses E-cadherin expression and enhances melanoma invasiveness. Cancer Res. 2008;68:7872–81.
Burgucu D, Guney K, Sahinturk D, Ozbudak IH, Ozel D, Ozbilim G, Yavuzer U. Tbx3 represses PTEN and is over-expressed in head and neck squamous cell carcinoma. BMC Cancer. 2012;12:481.
Richardson SR, Morell S, Faulkner GJ. L1 retrotransposons and somatic mosaicism in the brain. Ann Rev Genet. 2014;48:1–27.
The authors would like to extend their thanks to Dr. Ian Adams (Edinburgh University) for his invaluable and insightful comments on the manuscript.
VP-P and JJ were funded by Cancer Research Wales project grants and a Gwynedd Heamatology project grant. AH, MA and NOA were funded by award from the Kingdom of Saudi Arabia. JF was funded by OMICS Centre Graz grant of the Austrian Ministry for Science, Research and Economy.
Availability of data and materials
The datasets analyzed during the current study are available from The Cancer Genome Atlas (http://cancergenome.nih.gov).
VP-P, AH, JJ, NOA, MA, LP designed and performed experiments. JF and GGT carried out analysis of RNA-seq data and Kaplan-Meier analyses. VP-P, JF, JJ, LP, JAW and RJM drafted the manuscript. JAW and RJM designed experiments and managed the project. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Use of mice was approved by the Cardiff University ethics committee.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Human cancer cell lines used in this study. (DOCX 13 kb)
PCR primers used in the primary study. (DOCX 12 kb)
RT-qPCR analysis of 52 transcripts in TEX19 depleted cancer cell lines. The 52 transcripts were determined as the top hits (P < 0.01) from the RNA-seq data for transcript changes in SW480 (see Additional file 8; Figure S5). (DOCX 21 kb)
TEX19 is required for proliferation in cancer cells. a siRNA depletion of TEX19 mRNA in SW480 using siRNA B results in loss of proliferative potential (line plot * ≤ 0.01). RT-qPCR analysis of TEX19 mRNA levels at day 8 is given (bar chart; * ≤ 0.05; *** ≤ 0.001). Western blot analysis showing TEX19 depletion at 8 days is given (right). b siRNA depletion of TEX19 mRNA in HCT116 using siRNA A results in loss of proliferative potential (line plot * ≤ 0.01). RT-qPCR analysis of TEX19 mRNA levels at day 7 is given (bar chart; * ≤ 0.05; *** ≤ 0.001). Western blot analysis of TEX19 levels were not taken for this experiment (ND). c siRNA depletion of TEX19 mRNA in H460 using siRNA A results in loss of proliferative potential (line plot * ≤ 0.01). RT-qPCR analysis of TEX19 mRNA levels at day 8 is given (bar chart; * ≤ 0.05; *** ≤ 0.001). Western blot analysis showing TEX19 depletion at 8 days is given (right). d siRNA depletion of TEX19 mRNA in NTERA2 using siRNA B results in loss of proliferative potential (line plot * ≤ 0.01). RT-qPCR analysis of TEX19 mRNA levels at day 8 is given (bar chart; * ≤ 0.05; *** ≤ 0.001). Western blot analysis showing TEX19 depletion at 8 days is given (right). e Western blots showing siRNA A treatment results in depletion of TEX19 protein in SW480 cells. (PPTX 285 kb)
TEX19 is required for cancer progenitor/stem-like cell self-renewal. Sphere derived SW480 and NTERA2 cells were subjected to the extreme limiting dilution assay with siRNA depletion of TEX19. SW480 cells were treated with siRNA B and NTERA2 cells were treated with siRNA A. For both cell types there is a statistically significant difference between the TEX19 specific siRNA and the control siRNA indicating a need for TEX19 for self-renewal (* ≤ 0.01). (PPTX 86 kb)
Over expression of TEX19 does not alter the proliferative potential of SW480 cancer cells. TEX19 was introduced into SW480 cells under a DOX inducible promoter. Cell treated with DOX induced TEX19 expression (RT-qPCR at 8 days shown in the right hand bar graph) do not have increased or reduced proliferation (left hand plot). (PPTX 13327 kb)
Induction of a TEX19 specific shRNA reduces proliferation of HCT116 cells. Left: A TEX19 specific DOX inducible shRNA was integrated into HCT116 cells. Treatment with DOX results in a significant reduction in HCT116 proliferative capability (* ≤ 0.05). Right: RT-qPCR showing levels of TEX19 mRNA depletion. (PPTX 77 kb)
TEX19 regulates 80 protein coding gene transcripts in cancer cells: a Heat map showing the pattern of changes in protein coding transcripts in SW480 cells depleted for TEX19 mRNA. b List showing all the significant (P ≤ 0.05) log2 fold changes of protein coding transcripts in SW480 following depletion of TEX19 mRNA. Red bars indicate a reduction in transcripts; blue bar indicates an increase in transcripts. TEX19 is indicated in bold. ‘Inf’ represents infinite (positive Inf values indicate that genes were switched on from a previously undetectable state, whereas negative Inf values indicate that a given gene is switched to a state where no transcripts are detectable following siRNA treatment, but were prior to treatment). (PPTX 170 kb)
Table of cancer data sets analyzed. (DOCX 14 kb)
Kaplan-Meier plots for renal cancer and glioma. a Kidney renal clear cell carcinoma (KIRC) has a reduced overall survival when there is high TEX19 expression. Populations are divided by median TEX19 expression (red = high; grey = low). Dashed lines are 95% confidence intervals. b Kidney renal cell carcinoma (KIRP) has a reduced overall survival when there is high TEX19 expression. Populations are divided by median TEX19 expression (red = high; grey = low). Dashed lines are 95% confidence intervals. c There is a marginal, but significantly better overall survival for lower grade glioma (LGG) patients with high levels of TEX19 expression. Populations are divided by median TEX19 expression (red = high; grey = low). Dashed lines are 95% confidence intervals. (PPTX 95 kb)
Kaplan-Meier plots for lung and cervical cancer split by the highest 25% (red) vs. lower 75% (grey) for TEX19 expression (excluding RNA-seq sets without full clinical data). a Lung adenocarcinoma (LUAD) has reduced overall survival when there is high TEX19 expression. Dashed lines are 95% confidence intervals. b Cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC) have reduced overall survival when there is high TEX19 expression. Dashed lines are 95% confidence intervals. (PPTX 44 kb)
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Planells-Palop, V., Hazazi, A., Feichtinger, J. et al. Human germ/stem cell-specific gene TEX19 influences cancer cell proliferation and cancer prognosis. Mol Cancer 16, 84 (2017). https://doi.org/10.1186/s12943-017-0653-4
- Cancer-testis gene
- Cancer prognosis
- Cell proliferation
- Soma-to-germline transition