The H19 Long non-coding RNA in cancer initiation, progression and metastasis – a proposed unifying theory
© Raveh et al. 2015
Received: 23 June 2015
Accepted: 20 October 2015
Published: 4 November 2015
The imprinted oncofetal long non-coding RNA (lncRNA) H19 is expressed in the embryo, down-regulated at birth and then reappears in tumors. Its role in tumor initiation and progression has long been a subject of controversy, although accumulating data suggest that H19 is one of the major genes in cancer. It is actively involved in all stages of tumorigenesis and is expressed in almost every human cancer. In this review we delineate the various functions of H19 during the different stages in the complex process of tumor progression. H19 up-regulation allows cells to enter a “selfish” survival mode in response to stress conditions, such as destabilization of the genome and hypoxia, by accelerating their proliferation rate and increasing overall cellular resistance to stress. This response is tightly correlated with nullification, dysfunction or significant down-regulation of the master tumor suppressor gene P53. The growing evidence of H19’s involvement in both proliferation and differentiation processes, together with its involvement in epithelial to mesenchymal transition (EMT) and also mesenchymal to epithelial transition (MET), has led us to conclude that some of the recent disputes and discrepancies arising from current research findings can be resolved from a viewpoint supporting the oncogenic properties of H19. According to a holistic approach, the versatile, seemingly contradictory functions of H19 are essential to, and differentially harnessed by, the tumor cell depending on its context within the process of tumor progression.
KeywordsH19 miR-675 Tumorigenesis Proliferation Differentiation EMT MET Genomic instability miR-200 let-7
Tumorigenesis is a multistep process that involves both the neoplastic tissue and its surroundings. In order to survive and flourish, cancer cells acquire a unique genetic background, proliferate rapidly, evade growth suppressors, cell death pathways and immune system attacks, and resist multiple drug treatments. Cancer cells are experts in managing hypoxia and stress conditions by recruiting blood supply to the neoplastic tissue, adjusting metabolically and adopting the plasticity that should enable epithelial to mesenchymal transition (EMT), metastasis and colonization at secondary sites . In many aspects, a cancer cell resembles an embryonic cell: they share extraordinary plasticity, proliferation, motility and invasiveness capabilities, as well as the ability to make metabolic adjustments and other attributes, all orchestrated by common molecular pathways and epigenetic patterns .
One of the pivotal players in both embryonic development and tumorigenesis is the oncofetal lncRNA gene H19. H19, a maternally expressed and paternally imprinted 2.7 kb gene, resides close to the telomeric region of chromosome 11p15.5 and is reciprocally imprinted and regulated with its neighboring gene IGF2. Its genomic locus is rich in transcript coding sequences residing on both strands, as we have discussed elsewhere . However, one of the most important transcripts in the H19 locus is miR-675, a highly conserved micro-RNA that resides within exon-1 of the H19 gene.
Recent studies have highlighted the important roles of H19 during the complex process of tumorigenesis, starting from the early stages that involve translational deregulation and genomic instability, through proliferation imbalance and stress management to metastasis. In this article we review the role of H19 in the tumorigenic multistep process and show how H19 touches almost every aspect of tumorigenesis. We also describe how H19 functions as an initial tumorigenic output component in the mammalian feedback system responding to various stress conditions. We suggest a general unifying theory that may answer some of the disputes and discrepancies that have arisen in regard to the fundamental characteristics of the H19 gene.
H19 mechanism of action
H19 has a highly conserved secondary structure. This evolutionary conservation suggests that H19's function is structure-dependent . H19's function can be dissected into two major functions; a reservoir of miR-675 that suppresses its targets [5, 6], and a modulator of micro-RNAs or proteins via their binding.
MiR-675 targets a myriad of transcripts in a cellular-context-dependent manner . For example, miR-675 directly downregulates Igf1r , Smad1, Smad5, and Cdc6 ,Cadherin-11 , Cadherin-13 , Rb , Runx1 , Nodal Modulator 1 , TGFBI  CALN1 , and MITF . Indirect targets of miR-675 were also reported and some of them will be mentioned below.
Increasing data suggests a role for the full length H19 transcript as a decoy for micro-RNAs that modulates their availability and suppresses their activity [16–18]. H19 was also found to interact with transcription-repressors and guide them to specific loci; H19 binds the methyl-CpG–binding domain protein 1 MBD1 and recruits it to some of its targets (including H19’s reciprocally imprinted gene Igf2), thus enables the maintaining of repressive H3K9me3 histone marks in their loci . H19 also interacts with enhancer of zeste homolog 2 (EZH2), a histone H3 Lys 27 (H3K27) methyltransferase, that represses gene expression as part of the Polycomb-Repressive Complex 2 (PRC2) . In fibroblasts, H19 RNA itself is intracellularly sublocalized in lamellipodia and perinuclear regions through the binding of its 3’ to PTB (polypyrimidine tract-binding protein) and to 4 molecules of IGF2 mRNA-binding protein 1 (IGF2BP1) . In gastric cancer, H19 was also found to bind P53 and partially inactivate it , and to bind ISM1 (Isthmin 1) in what seems to support a higher expression of this protein . H19 was also found to bind the RNA binding protein K homology-type splicing regulatory protein (KSRP) . This interaction supports KSRP targeting of unstable mRNAs, such as Myogenin, that leads to their subsequent decay. By that, H19 maintains an undifferentiated cellular state.
H19 and P53: A tight relationship
Since p53 is the major tumor suppressor gene in cancer, it is not surprising that H19 and p53 are mutually counter-regulated. Not only does P53 repress the promoter activity of the H19 gene [24, 25], it also epigenetically suppresses H19 expression in vivo by inducing DNA demethylation of the imprinting control region (ICR) upstream to the H19 gene . We also have shown that hypoxia triggers H19 expression in p53 deficient cell lines , as will be later discussed. Moreover, it was recently found in bladder cancer cells that H19 derived miR-675 has a major role in inhibiting p53 and p53-dependent protein expression . On the other hand, in gastric cancer cells H19 RNA was shown to interact with P53 protein, causing its partial inactivation , in what seems to be a negative feedback loop. As will be discussed below, this P53-H19 interplay is fundamental to understanding the role of H19 in tumorigenesis.
H19 and genomic instability
Chromosomal instability (CIS) and overall genomic instability (including chromosomal aberrations and other mutations) were recognized as early as the beginning of the 20th century by Bovery as one of the most basic tumor-enabling attributes of cancer (reviewed in [29, 30]). In the somatic cell, chromosomal stability and a balanced number of paired chromosomes are essential for appropriate gene expression and chromosome segregation during the normal cell cycle. Thus, the cell cycle process is kept under strict molecular surveillance to prevent unbalanced segregation, replication of damaged DNA and incomplete replication . However, when vital caretaker genes (“genome guardians”) and gatekeeper genes (“proliferation buffers”) such as p53, Rb and others are dysfunctional, as in tumor initiation, the way is wide open for the accumulation of mutations and chromosomal missegregations . These not only make the cell susceptible to future damage but also burden it with immediate metabolic stress, forcing the cell to accommodate to the alterations in its genomic content. On the other hand, it is these very genomic alterations that may confer the cell the genetic diversity necessary to manage stress [32, 33]. This possible advantage may provide an explanation for the various effects of hypoxic stress on genetic instability ; for the common polyploidy found in liver cells, which are under continuous oxidative and cytotoxic stress or following hepatectomy; and for other mechanical and metabolic stress conditions in which polyploidy is commonly reported (reviewed in ). As a comprehensive theory to explain the high rate of aneuploidy in tumors [36, 37], it was suggested that polyploidy is an intermediate, but sometimes unstable stage, that tends to attenuate proliferation (reviewed in [38, 39]) but also serves as a gateway karyotype to aneuploidy [30, 35, 40]. Moreover, the low proliferation rate of polyploid cells confers on them resistance to drugs that target actively cycling cells. Polyploid cells, due to their multiple but diverse chromosomes, have an inherent genetic system that buffers against deleterious mutations. Polyploidy cells also adopt attributes of stem cells, namely plasticity and metabolic reprogramming (reviewed in ), which make them an excellent starting point for more aggressive tumor descendants.
Recent studies by Zipori and colleagues [41, 42] have shown that H19 regulates polyploidy and that H19 expression is positively correlated with polyploidy suppression and tumorigenesis. These studies revealed that polyploid bone marrow mesenchymal stromal cells (BM MSC) have far less tumorigenic potential than diploid ones, have higher resistance to UV irradiation, and differ from diploid cells by their significantly lower H19 expression levels. This correlation between H19 expression and ploidy level was further demonstrated in mouse liver cells, which are diploid in the suckling mouse but drifted toward polyploidy with age progression while significantly decreasing their H19 expression. Moreover, H19 knock-down in diploid MSC caused them to drift toward polyploidy and reduced their tumorigenic attributes and UV sensitivity. H19 knock-down also improved the efficiency of artificial tetraploidization in these cells. On the other hand, artificial tetraploidization itself reduced H19 levels, suggesting a negative feedback loop mechanism in which H19 represses polyploidy, which in turn represses H19 expression to maintain a polyploid state.
However, comparison of BM MSC with adipose MSC revealed lower H19 expression in the latter cells, accompanied by diploid nature and a higher P53 level . As both of the cell types had WT p53 gene, the differences were probably due to epigenetic regulation of p53 . Indeed, when challenged with UV radiation, oxidative stress and chemotherapy, BM MSC responded by elevated expression of P53’s target genes, although the response was greater than in adipose MSC due to the relative low basal activity of p53 in BM MSC. This study provides further support for P53-H19 counter-regulation. Surprisingly, H19 levels were also reported to increase in tetraploid MSC in response to UV radiation .
Despite the above, H19 transient overexpression in diploid cells will not necessarily prevent polyploidy. In P53 WT hepatocellular carcinoma (HCC) cells, miR-675 transient overexpression actually increased the rate of tetraploid cells in culture . However H19 and its derived miR-675 can down-regulate P53 activity, and this temporary P53-deficiency-related stress may be the cause of polyploidy, in accordance with the mechanism suggested above.
The mutually exclusive nature of polyploidy and H19 expression may also be inferred by the various reported effects of the natural drug curcumin. Curcumin treatment of various tumor cell types resulted in H19 suppression . As curcumin induces mitotic abnormalities and subsequent cytokinesis failure that are usually the basis of polyploidy , the suppression of H19 by curcumin aligns with the genome destabilization effects of curcumin.
It is worth mentioning here, however, that the mechanism by which H19 represses polyploidy is still unclear. The PI3K/Akt signaling pathway was recently proposed as a good candidate to connect the alternate cellular fates of high H19 or polyploidy . We have previously shown that PI3K/Akt active signaling upregulates H19 to promote metastasis . Apparently, PI3K/Akt is also critical for the polyploidization phenomenon in the murine liver during weaning progression . It is therefore tempting to assume that the PI3K pathway is upstream to the two alternative pathways that lead the stressed cells in opposite directions. This suggestion is further strengthened by the fact that P53 negatively regulates the PI3K pathway via transcriptional activation of its pivotal negative regulator, PTEN (which is also a negative regulator of H19 and miR-675 ). Moreover, P53 can also repress PI3K downstream effectors (reviewed in ).
Another candidate upstream of H19/Polyploidy fates fork is PARP-1 (poly ADP-ribose polymerase). PARP-1, a DNA damage repair enzyme and a positive regulator and stabilizer of P53 , was reported as a repressor of H19 expression in ES cells . But PARP-1 also prevents polyploidy as was demonstrated in PARP-1 null fibroblasts . Therefore, it is also possible that impaired PARP-1, which is combined with, or resulting in, P53 reduction, accounts for either H19 upregulation or polyploidization.
H19 and P53 at the junction of the hypoxic stress response and proliferation
One of the fundamental hallmarks of cancer is uncontrolled, chronic cell proliferation. However, it is not only an attribute of cancer but also one of the major engines that drive carcinogenesis [55, 56]. The higher the rate of proliferation, the greater the risk of acquiring either antimorphic mutations (resulting in oncogenic activity) or amorphic mutations (in tumor suppressor genes (TSGs)) that may further promote proliferation . Two major regulators of cell proliferation and TSGs, P53 and RB, are strongly affected by H19, which counteracts their action. As mentioned above, P53 is an H19 suppressor.
Hypoxia is a common stress condition in tumors. In addition to the abnormal vascularization commonly affecting their essential nutrient and gas exchange , the high proliferation rate of transformed cells impedes their access to normal blood supply. Thus, it is not surprising that hypoxia is a characteristic of all solid tumors . Hypoxia, especially of the acute type, also tends to induce a more aggressive, invasive and resistant tumor phenotype [59, 60].
We have previously shown that hypoxia or artificial-hypoxia conditions induce H19 transcription  when P53 is null or impaired . Hence, under in vivo conditions, p53 mutations which are pro-proliferative can easily lead to tissue hypoxic foci in which H19 expression is subsequently induced. As we have demonstrated , HIF1-α mediates H19 induction upon hypoxia when p53 is impaired, possibly due to the loss of P53 inhibitory effect on HIF1-α. Apparently, nuclear localization of P53, rather than its tetramerization (which is essential for the translational activity of P53 protein), is essential for H19 inhibition .
It has been shown in both liver and bladder cancer cells, both in vitro and in vivo, that upon induction, H19 supports tumor growth by suppressing the cyclin-dependent kinase inhibitor p57kip2 (CDKN1C) and other putative tumor suppressor genes, while upregulating pro-oncogenic genes (like cyclin E2 and others) . H19 suppression of p57kip2 was evident also upon serum depletion, a condition that usually induces p57kip2 mediated quiescence . Hence, once induced, H19 may worsen the hypoxic stress, initiating a positive feedback loop that further promotes proliferation and subsequent hypoxia. At the same time, as evident from our differential transcriptome analysis studies conducted both in liver and bladder cancer cell lines [61, 62], H19 enhances tumor survival under harsh conditions. H19 upregulates transcription of angiogenic genes and thus enables blood supply to the proliferating tumor. H19 also suppresses apoptotic-signaling-related gene transcription (among them DNA-damage sensitive genes, like the DDIT3 gene), and promotes transcription of survival-related and chemo-resistance related genes [61, 62]. By resisting apoptosis under hypoxia, which is in itself a mutagenesis supporting condition , H19 allows further accumulation of deleterious mutations. Cells under acute hypoxia are prone to experience subsequent oxidative stress, caused by rapid hypoxia/anoxia and reoxygenation transitions, due to the abnormal vasculature in the tumor niche . Intriguingly, it was reported that H19 post-transcriptionally upregulates Thioredoxin (Trx) protein in cancerous epithelial mammary cells . Trx, a component in the system controlling the reduced intracellular redox environment and an abundant anti-apoptotic protein in many cancers, provides defense against oxidative stress . Thus, it is possible that H19 also confers resistance to oxidative stress on the cancerous tissue. Indeed, H19 increased the promoter activity of the survival factor NF-KB, a validated target of Trx, as shown in luciferase assays .
Interestingly, another unexplored possible connection between oxidative stress and H19 promoted proliferation may be suggested from its proliferative effect in bladder cancer cells that was reported to be exerted by upregulation of Id2 (inhibitor of DNA binding/differentiation 2) . It was reported elsewhere that the levels of glutathione, a physiological antioxidant, are positively correlated with ID2 levels . Hence, it seems that Id2’s sensitivity to hypoxic stress may be circumvented by H19 which may upregulate Id2 regardless of hypoxic status.
In order to promote G1/S transition during the cell cycle, H19 needs to avoid suppression by P53 but also by Rb, another classic suppressor of G1/S transition and subsequent proliferation. One of the key proteins suppressed by Rb is E2F1, a transcription factor that binds to and activates H19 promoter, as was shown in breast cancer cells . Since E2F1 is known as a G1/S transition promoting factor during the cell cycle, it is reasonable to assume that H19 mediates the pro-proliferative function of E2F1 . Indeed, silencing of H19 in breast cancer cells reduces their proliferation while H19 overexpression accelerates cell cycle progression [68, 69]. Moreover, it was experimentally shown in breast cancer cells that Rb indirectly suppresses H19 expression by repressing E2F1 , while in colorectal cancer cells  and in hepatocellular carcinoma cells , H19 derived miR-675 negatively regulates Rb expression. This phenomenon was verified in a transgenic mouse model of prostate cancer (Pten and Zbtb7a double knockout mice), in which Sox9 is upregulated and suppresses Rb via miR-675 . The above data, when integrated, suggest a feedback loop in which upregulated H19 further promotes proliferation by repressing Rb . This loop may be accelerated in response to stress, since H19 is upregulated following release from quiescence that was induced by serum starvation, and E2F1 is a known major player in quiescence to proliferation transition . Hence, H19 responds not only to hypoxic stress but also to serum-depletion-induced quiescence by accelerating proliferation, dependent on the loss or dysfunction of critical TSGs.
H19 in epithelial to mesenchymal transition (EMT) and its converse MET process: a matter of circumstances?
Metastases are the major cause of cancer related death. Although proliferation and metastasis are uncoupled processes, it is plausible, at least according to the linear progression paradigm that suggests an evolutionary progress towards metstasis, that hyper-proliferation increases the somatic mutational rate that may promote a metastatic transition [1, 71, 72]. But regardless of its involvement in proliferation that may indirectly promote malignancy, recent studies by us and others show that H19 promotes tumor metastasis by direct involvement in malignant processes. Metastasis is a multi-step process consisting of apparently contrary sub-processes. EMT requires de-differentiation of epithelial cells in order to enable dissemination, migration through the extra cellular matrix (ECM) and intravasation into blood vessels that will carry them to their secondary site. Once extravased to the secondary site, the tumor cell goes through the reverse mechanism of mesenchymal to epithelial transition (MET) that resembles re-differentiation, and then (even decades later, in some cancers) proliferates and colonizes to become a secondary tumor . Controversial reports describe H19 as either a pro-differentiation or a pro-proliferation factor; either an EMT promoter or an MET promoter. We will discuss these discrepancies in the context of metastasis as a whole.
H19 in EMT
We have recently shown that numerous bona-fide EMT inducers also induce H19/miR-675 expression . In HCC cells, TGF-β has been shown to induce H19 expression via activation of the PI3K/Akt signaling pathway. This TGF-β dependent induction of H19 has been recently corroborated in an experimental model of colorectal cancer . We have also found that H19 is essential for upregulation of the EMT related transcription factor Slug by TGF-β. In addition, hypoxia induces H19 and miR-675 as well as the EMT markers Slug and Snail in breast cancer cells. Association of drug resistance with elevated levels of H19 and Slug was demonstrated in a cisplatin resistant ovarian cancer cell line, in which H19 upregulates, apparently indirectly, the promoter activity of Slug, which upregulates H19 in a positive feedback loop. We have also shown that in a pancreatic cancer cell line E-cadherin is totally ablated upon H19 expression as long as H19’s miR-675 seed region is intact. This total ablation of E-cadherin was also shown in HCC and lung carcinoma cells overexpressing H19, together with the upregulation of the mesenchymal N-cadherin . Besides enabling dissemination, E-cadherin loss is an essential step towards enabling cells to adopt their cytoskeleton to migrational mode . Indeed, our studies suggest that H19 participates in the invasion process of cancer cells; Forced expression of H19 improves HCC cell invasiveness in an in vitro assay. Hepatocyte growth factor/scatter factor (HGF/SF), a ligand of the tyrosine kinase c-Met receptor named after its pro-migratory attributes, enhances H19 promoter activity in treated cells in culture. Moreover, anchorage independent growth assays suggested that H19 is essential for HGF/SF induced scattering morphology and colony formation in soft agar .
There is a large amount of in vivo evidence supporting the pro-metastatic nature of H19. Sub-colonies of a mammary gland tumor cell line differ not only in their ability to migrate to the lung and colonialize there, but also by their relative H19 expression levels [48, 74]. In an experimental mouse model of lung carcinoma metastasis that was induced by intravenous injection of cells, cells overexpressing H19 manifested improved ability to metastasize in comparison to control cells transfected with empty vector. Examination of lungs for micrometastases (that may serve as a measure of ability to metastasize) and macrometastes (visible metastases; a possible measure of proliferation) revealed that overexpression of H19 resulted in an increased number of lung micrometastases compared to control mice. Macrometastes were only seen in mice injected with cells overexpressing H19, suggesting that the pro-proliferative attributes of H19 are also manifested at the secondary site . In light of all the above, it is not surprising that high H19 levels are present in human biopsies of all common metastatic sites tested in our study, regardless of tumor primary origin .
Recently, and concurrently with our work, other researchers have found additional key players in the EMT process that are linked to H19, thus extending the network of routes through which H19 exerts its metastatic function. In bladder cancer cells, H19 was found both in vitro and in vivo to promote EMT, down-regulation of E-cadherin and cell migration. By association with enhancer of zeste homolog 2 (EZH2), a well-established mediator of tumor metastasis , H19 upregulates Wnt/β-catenin signaling, which in turn represses E-cadherin expression .
H19 can also promote metastasis through sponging and sequestering of the first identified micro-RNA, let-7 . This let-7-sponging function of H19, which is conserved in both human and mouse, does not affect let-7 RNA levels but does affect its function as a suppressor of differentiation-suppressing-genes in muscle cells (such as Hmga2 and DICER). Hence, H19 may actually serve as a differentiation suppressor . In accordance with its negative role in muscle differentiation, it was recently reported that H19 may act as a scaffold that favors KSRP-mediated degradation of myogenin transcript to subsequently contribute to the maintenance of the undifferentiated state of C2C12 muscle cells . Given the differentiation suppressive attributes of H19 in muscle, it is not surprising that in pancreatic ductal adenocarcinoma, as well as in ovarian cancer and uterine serous carcinoma cell lines, sequestering of let-7 by H19 is essential for H19 function in EMT processes, including cell invasion and migration [76, 77]. In ovarian cancer and uterine serous carcinoma cell lines, the pro metastatic oncogene c-Myc [78, 79], which upregulates H19 , is also its indirect target, due to removal of c-Myc let-7-mediated repression. The anti-diabetic drug Metformin can vitiate the metastatic phenotype of ovarian cancer cell lines, apparently due to induction of hypermethylation at the H19 locus . In this context it is highly intriguing to note that the H19/let-7 axis plays another role in muscle: while let-7 inhibits glucose uptake and promotes glucose intolerance, H19 upregulates insulin receptor in diabetic conditions to increase glucose uptake and is downregulated upon hyperinsulinemia . Exactly how Metformin’s negative effect on H19 aligns with its function in increasing glucose uptake in skeletal muscle  (a function which is also attributed to H19) remains to be explored. Nevertheless, let-7 is not only sequestered by H19, but also can destabilize it under hyperinsulinemia conditions (as opposed to the highly stabile status of H19 in normal differentiated muscle ); therefore it exerts a negative feedback cycle to repress its negative regulator H19 .
A recent study contradicts the above findings since it reported pro-differentiation properties of H19 and its derived miR-675 forms in muscle . Descriptive evidence indicates that miR-675 is upregulated gradually upon murine skeletal muscle injury in vivo to mediate muscle regeneration and differentiation through inhibition of the BMP-pathway components. This study however found that let-7 was not induced in their cell culture model during differentiation, even though the same muscle cell line was used. Thus, it is possible that H19 may be capable of totally opposite functions, with the specific functions being largely dependent on cellular context and partners. We will come back to this point below.
The most important lesson that can be learnt from the H19/let7 axis findings is that positive correlation between a specific factor and a phenotype may suggest the opposite to what one would assume. Instead of being a differentiation factor in muscle cells, as has been thought till recently, H19 is upregulated during myo-differentiation mainly in order to counteract the pro-differentiation functions of let-7 . As H19 harbors not only let-7 binding sites (both canonical and non-canonical), but also other putative miRNA binding sites , it is plausible that other miRNA interplay with H19 in various ways. Indeed, it was recently reported that miR-106a is also sponged by H19 in both Hela cells and myoblasts . Another fascinating finding suggests that H19 promotes EMT by sponging two EMT repressors, miR-134 and miR-200 in colorectal cancer metastasis . It would seem that the finding of differentiation-correlated expression of H19 in human BM MSC , for example, should prompt us to search for possible H19 targets/partners such as let-7 or miR-106a.
Another characteristic of an EMT process is the stemness phenotype of the transformed cells. The stem cell-like state of cells during EMT enables them to self-renew and proliferate while transforming, disseminating and migrating . Interestingly, H19 maternal expression which directly impacts upregulation of Igf2 and Igf1r, together with the repressive effect of miR-675 on Igf1r , may take part in the maintenance of adult haematopoietic stem cell quiescence . Furthermore, a recent study of prostate and breast human cell lines revealed a putative role of stemness for H19, since its expression was positively correlated with stem cells markers and pluripotency factors. H19 was also found to control the expression of two major pluripotency factors, Oct4 and Sox2, which apparently regulate H19 in an amplification feedback loop .
H19 may act differentially depending on developmental stage
In spite of the strong supportive evidence for H19 and miR-675 involvement in EMT, which is regarded as a de-differentiation/trans-differentiation process, there is enough contradictory data to position H19 as a tumor suppressor and a pro-differentiation factor. However, when the data are carefully examined, it would seem that most of the controversy may be solved by dividing the functions of H19 into two developmental periods. We propose that in the embryonic period H19 mostly promotes differentiation, while in the adult it is rarely expressed in noncancerous tissues and has tumorigenic properties. Moreover, nullification of H19 or severely abrogating its function in cells at early developmental stages may impact its function at later stages, making the cells more liable to tumorigenesis. The significance of the embryonic expression of H19 for later stages is implied as H19 expression in embryonic samples controls the gene expression of several imprinted genes of the imprinted gene network (IGN) by facilitating deposition of repressive histone marks on their differentially methylated regions , mostly by recruiting MBD1 protein to their loci . Regardless of the different nature of the genes H19 controls by this mechanism (for example: the cancer related Igf2 on one hand and cell cycle inhibitor Cdkn1c and Igf2r growth repressor on the other), the model used to show H19 control over the IGN was based on H19 KO (knockout) mice manifesting an overgrowth phenotype and subsequent mating of H19 transgenic with the KO mice to rescue the phenotype . Assuming that the embryonic stage of H19 expression is a critical stage that impacts a set of other imprinted genes, it is not impossible that conditional silencing of the H19 in the adult would not have rescued the overgrowth phenotype, or that conditional expression of H19 in the adult would not have achieved the phenotypic rescue reported. According to our hypothesis, in the second scenario, induction of H19 at later stages may even worsen the tumorigenic phenotype. This suggested distinction between embryo and adult was previously implied by Gabory and colleagues, who studied the H19 KO mouse model described above .
In support of our suggestion, H19 expression leads to growth retardation, abrogation of clonogenicity and impaired in vivo tumorigenesis, but these findings were manifested in embryonic tumor cell lines . Another comprehensive study in murine KO models isolated the H19 deletion effect from the effect of Igf2 overexpression, which commonly accompanies H19 deletion, and showed in several tumor models that H19 has tumor suppressing properties . However the researchers that used this murine model also disregarded possible potential implications of lack of H19 expression during embryonic stages. Moreover, they used ES cells in one of their models. The researchers also admit that H19 KO mice do not tend to spontaneously develop tumors, which indicates that H19 is not a tumor suppressor per se but rather its deletion increases cells tendency for cancer. We suggest that this deletion is critical at the embryonic stage and can also impact later stages.
The emerging role of H19 in MET
As we have seen above, H19 plays a role in EMT. Can it also play a role in MET? Is MET, in its literal meaning of re-differentiation, needed for metastasis at all where H19 participates? Metastasis can be explained as a result of either MET, the process of re-differentiation after intravasation of the tumor cell to its secondary site, or plasticity and stemness of the metastatic cells . Plasticity does not require continuous genetic alterations, except for initiator mutations. Instead, cells adopt semi-stemness and primitive differentiation attributes that confer on them the ability to accommodate and react to environmental cues, while keeping their high proliferative potential. Plasticity may be supported by reversible epigenetic patterns but other mechanisms are also possible.
We previously mentioned that H19 is highly abundant in secondary tumors and in cell lines that complete their journey to the secondary site. We have reported that miR-675 is essential for EMT, ablation of epithelial markers and upregulation of mesenchymal markers as found in hepatocellular carcinoma in vitro. An apparently conflicting report indicated that miR-675, in another hepatocellular carcinoma cell line model, is an MET promoter . While increasing proliferation and repressing Rb, miR-675 altered cellular morphology, upregulated epithelial markers and downregulated the mesenchymal ones, reduced invasive potential, and increased anchorage-independent growth capacity. In addition, it downregulated the EMT key mediator, Twist1 (as opposed to its high positive correlation with H19 in the murine metastasis model of 4 T1 breast cancer cell line in which Twist was initially identified as a metastasis marker ). In prostate cancer cells, miR-675 was also reported to suppress the extra cellular matrix TGF-β induced (TGFBI) protein transcript, which enhances motility and invasion in metastasis. . Those findings also align with the study that claimed a pro-differentiation role for miR-675 in muscle, as mentioned above .
“Selfish” H19 promotes metastasis along its seemingly contradicting stages
Another fascinating regulatory level lies in the inhibitory circuit between Snail, the repressor of miR-34 and miR-200, and HNF4α, which, contrary to Snail, promotes differentiation [92, 95]. HNF4α is a transcription factor which is abundant in both hepatoblasts (the liver bipotential cells that during development progressively differentiate into hepatocytes and cholangiocytes), and in the differentiated hepatocytes. However, it turns out that the distinct functions of HNF4α at different developmental stages of liver cells, from embryo to adult, are due to the developmentally dependent binding pattern of HNF4α to differential enhancers. Intriguingly, one of the HNF4α enriched enhancers in embryonic liver belongs to the H19 gene. Moreover, it was shown that the transcriptional co-regulator Yap1, which is the nuclear effector of the Hippo signaling pathway, induces the binding of HNF4α to H19 enhancer and upregulates its expression in the embryonic liver via activation of the transcription factor TEAD, a classical cofactor of Yap1 . Yap1 promotes metastasis via TEAD , and was recently found to upregulate H19 in osteosarcoma in response to Hedgehog signaling activation .
In light of the above, we suggest that H19 may support both EMT and MET (Fig. 3), conferring the cell the plasticity needed throughout the stages of transformation. H19 plays a role in EMT that eventually consolidates with that of ZEB1 in EMT, due to their shared extracellular EMT inducers. Moreover, EMT inducers such as TGF-β also have a negative impact on miR-200 expression [99, 100], an impact that is further supported by H19’s direct sponging of miR-200. H19 also induces Snail expression as we have previously reported. However, in regard to the ZEB1–miR200 loop, H19 rather promotes the MET axis, apparently by interaction with a ribonucleoprotein complex that activates miR200 expression . This interaction may explain why in MET, H19 serves rather as an inducer of miR-200 than as its sponging repressor . Hence, upon reduction or removal of EMT extracellular inducers like TGF-β, or activation of Hedgehog signaling (an established Yap1 activator [98, 101]) or, possibly, inactivation of hippo signaling (which represses Yap1 activation), H19 shifts the cell to an “MET” state. This shift may be further supported by upregulation of ribonucleoprotein complexes, such as histone acetylases [93, 102], that compete for H19 binding to exert an MET-like phenotype.
It is also possible that H19 expression is alternatively induced by the converse transcription factors Snail and HNF4α in each of the opposite scenarios of EMT and MET. These two factors may not only suppress each other but also compete on binding to the H19 enhancer, though this suggestion should be further explored.
Of note, P53 is a known inducer of both miR-200 and miR-34 and hence supports MET (revieved in ). Nevertheless, we have pointed out above that P53 and H19 are, in general, mutually regulated. It is therefore appealing to suggest that H19 is an alternative, P53 independent MET promoter, which is more favorable to continuous cancer progression than to metastasis arrest given its contribution to both MET and EMT.
Other transcripts on the H19 locus
As we have reviewed extensively elsewhere , two major antisense transcripts reside on H19’s opposite strand; the 120 kb-long 91H transcript and the smaller ~6 kb HOTS transcript. The unstable 91H , as opposed to H19, is exclusively nuclear, however it shares some of H19 attributes. It is also induced during myoblasts differentiation and upregulated in cancer (due to RNA stabilization), as was shown in breast cancer cell lines. However its silencing, though it has negligible effect on H19 expression, reduces the expression of its reciprocally imprinted gene, Igf2, in contrary to H19’s suppressive effect on Igf2 expression . The HOTS transcript  encodes for nuclear protein in primates but lacks an open reading frame in mouse. It is still unclear whether it is an autonomous transcript or a part of 91H. The last option is less trivial, since, according to in vitro data, HOTS functions as a tumor-suppressor. Although loss of IGF2 imprinting leads to silencing of both H19 and HOTS, the expression of H19 and HOTS seems to be uncoordinated, as it is not mutually correlated across tissues. Moreover- expression in vitro of each does not affect significantly the expression of the other. Although the scanty data available as for the two H19 antisense transcripts is not concrete enough to conclude what their effect on H19’s role in tumorigenesis might be, and in spite of the mutually independent regulation between them and H19, they may counteract H19 function. A possible balance between H19 and its antisense transcripts may serve as an additional regulatory level that may dictate cellular fate.
We have also highlighted the importance of H19 during embryonic stages, proposing that at embryonic stages H19 acts mostly as a differentiation promoter. We have proposed that those stages may be vital for shaping H19’s role and functions throughout development and may impact its seemingly opposite tumorigenic roles in the adult.
Some of the suggestions and hypotheses raised here should be further examined and explored deeply. Although we have used as holistic an approach as we could, we are aware of the differences between models and conditions that were used in the reports we reviewed. Indeed, to establish our proposed paradigm of H19’s involvement throughout tumor progression from its initiative events of translational deregulation and genomic instability to metastasis and secondary colonization, H19 should be studied in one, holistic, induced metastasis model throughout cancer progression. In addition, a correlation should be determined between the apparent functions of H19, which is accompanied by a phenotypic output in the certain cell line of interest, and the dynamic levels of the major players in the EMT–MET switch this cell line expresses. Nevertheless, there is no doubt that H19 is tightly linked to tumorigenesis throughout all its stages. In view of its deep involvement in cancer, H19 should be placed in the center of the combat against cancer as a main therapeutic target and a cancer marker.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646–74. doi:https://doi.org/10.1016/j.cell.2011.02.013.PubMedView ArticleGoogle Scholar
- Ma Y, Zhang P, Wang F, Yang J, Yang Z, Qin H. The relationship between early embryo development and tumourigenesis. J Cell Mol Med. 2010;14(12):2697–701. doi:https://doi.org/10.1111/j.1582-4934.2010.01191.x.PubMed CentralPubMedView ArticleGoogle Scholar
- Matouk I, Raveh E, Ohana P, Lail RA, Gershtain E, Gilon M, et al. The increasing complexity of the oncofetal h19 gene locus: functional dissection and therapeutic intervention. Int J Mol Sci. 2013;14(2):4298–316. doi:https://doi.org/10.3390/ijms14024298.PubMed CentralPubMedView ArticleGoogle Scholar
- Juan V, Crain C, Wilson C. Evidence for evolutionarily conserved secondary structure in the H19 tumor suppressor RNA. Nucleic Acids Res. 2000;28(5):1221–7.PubMed CentralPubMedView ArticleGoogle Scholar
- Keniry A, Oxley D, Monnier P, Kyba M, Dandolo L, Smits G, et al. The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1r. Nat Cell Biol. 2012;14(7):659–65. doi:https://doi.org/10.1038/ncb2521.PubMed CentralPubMedView ArticleGoogle Scholar
- Cai X, Cullen BR. The imprinted H19 noncoding RNA is a primary microRNA precursor. RNA. 2007;13(3):313–6. doi:https://doi.org/10.1261/rna.351707.PubMed CentralPubMedView ArticleGoogle Scholar
- Dey BK, Pfeifer K, Dutta A. The H19 long noncoding RNA gives rise to microRNAs miR-675-3p and miR-675-5p to promote skeletal muscle differentiation and regeneration. Genes Dev. 2014;28(5):491–501. doi:https://doi.org/10.1101/gad.234419.113.PubMed CentralPubMedView ArticleGoogle Scholar
- Kim NH, Choi SH, Lee TR, Lee CH, Lee AY. Cadherin 11, a miR-675 target, induces N-cadherin expression and epithelial-mesenchymal transition in melasma. J Invest Dermatol. 2014;134(12):2967–76. doi:https://doi.org/10.1038/jid.2014.257.PubMedView ArticleGoogle Scholar
- Shi Y, Wang Y, Luan W, Wang P, Tao T, Zhang J, et al. Long non-coding RNA H19 promotes glioma cell invasion by deriving miR-675. PLoS One. 2014;9(1):e86295. doi:https://doi.org/10.1371/journal.pone.0086295.PubMed CentralPubMedView ArticleGoogle Scholar
- Tsang WP, Ng EK, Ng SS, Jin H, Yu J, Sung JJ, et al. Oncofetal H19-derived miR-675 regulates tumor suppressor RB in human colorectal cancer. Carcinogenesis. 2010;31(3):350–8. doi:https://doi.org/10.1093/carcin/bgp181.PubMedView ArticleGoogle Scholar
- Zhuang M, Gao W, Xu J, Wang P, Shu Y. The long non-coding RNA H19-derived miR-675 modulates human gastric cancer cell proliferation by targeting tumor suppressor RUNX1. Biochem Biophys Res Commun. 2014;448(3):315–22. doi:https://doi.org/10.1016/j.bbrc.2013.12.126.PubMedView ArticleGoogle Scholar
- Gao WL, Liu M, Yang Y, Yang H, Liao Q, Bai Y, et al. The imprinted H19 gene regulates human placental trophoblast cell proliferation via encoding miR-675 that targets Nodal Modulator 1 (NOMO1). RNA Biol. 2012;9(7):1002–10. doi:https://doi.org/10.4161/rna.20807.PubMedView ArticleGoogle Scholar
- Zhu M, Chen Q, Liu X, Sun Q, Zhao X, Deng R, et al. lncRNA H19/miR-675 axis represses prostate cancer metastasis by targeting TGFBI. FEBS J. 2014;281(16):3766–75. doi:https://doi.org/10.1111/febs.12902.PubMedView ArticleGoogle Scholar
- Li H, Yu B, Li J, Su L, Yan M, Zhu Z, et al. Overexpression of lncRNA H19 enhances carcinogenesis and metastasis of gastric cancer. Oncotarget. 2014;5(8):2318–29.PubMed CentralPubMedView ArticleGoogle Scholar
- Kim NH, Choi SH, Kim CH, Lee CH, Lee TR, Lee AY. Reduced MiR-675 in exosome in H19 RNA-related melanogenesis via MITF as a direct target. J Invest Dermatol. 2014;134(4):1075–82. doi:https://doi.org/10.1038/jid.2013.478.PubMedView ArticleGoogle Scholar
- Kallen AN, Zhou XB, Xu J, Qiao C, Ma J, Yan L, et al. The imprinted H19 lncRNA antagonizes let-7 microRNAs. Mol Cell. 2013;52(1):101–12. doi:https://doi.org/10.1016/j.molcel.2013.08.027.PubMedView ArticleGoogle Scholar
- Imig J, Brunschweiger A, Brummer A, Guennewig B, Mittal N, Kishore S, et al. miR-CLIP capture of a miRNA targetome uncovers a lincRNA H19-miR-106a interaction. Nat Chem Biol. 2015;11(2):107–14. doi:https://doi.org/10.1038/nchembio.1713.PubMedView ArticleGoogle Scholar
- Liang WC, Fu WM, Wong CW, Wang Y, Wang WM, Hu GX, et al. The LncRNA H19 promotes epithelial to mesenchymal transition by functioning as MiRNA sponges in colorectal cancer. Oncotarget. 2015;6(26):22513–25.Google Scholar
- Monnier P, Martinet C, Pontis J, Stancheva I, Ait-Si-Ali S, Dandolo L. H19 lncRNA controls gene expression of the Imprinted Gene Network by recruiting MBD1. Proc Natl Acad Sci U S A. 2013;110(51):20693–8. doi:https://doi.org/10.1073/pnas.1310201110.PubMed CentralPubMedView ArticleGoogle Scholar
- Luo M, Li Z, Wang W, Zeng Y, Liu Z, Qiu J. Long non-coding RNA H19 increases bladder cancer metastasis by associating with EZH2 and inhibiting E-cadherin expression. Cancer Lett. 2013;333(2):213–21. doi:https://doi.org/10.1016/j.canlet.2013.01.033.PubMedView ArticleGoogle Scholar
- Runge S, Nielsen FC, Nielsen J, Lykke-Andersen J, Wewer UM, Christiansen J. H19 RNA binds four molecules of insulin-like growth factor II mRNA-binding protein. J Biol Chem. 2000;275(38):29562–9. doi:https://doi.org/10.1074/jbc.M001156200.PubMedView ArticleGoogle Scholar
- Yang F, Bi J, Xue X, Zheng L, Zhi K, Hua J, et al. Up-regulated long non-coding RNA H19 contributes to proliferation of gastric cancer cells. FEBS J. 2012;279(17):3159–65. doi:https://doi.org/10.1111/j.1742-4658.2012.08694.x.PubMedView ArticleGoogle Scholar
- Giovarelli M, Bucci G, Ramos A, Bordo D, Wilusz CJ, Chen CY, et al. H19 long noncoding RNA controls the mRNA decay promoting function of KSRP. Proc Natl Acad Sci U S A. 2014;111(47):E5023–8. doi:https://doi.org/10.1073/pnas.1415098111.PubMed CentralPubMedView ArticleGoogle Scholar
- Dugimont T, Montpellier C, Adriaenssens E, Lottin S, Dumont L, Iotsova V, et al. The H19 TATA-less promoter is efficiently repressed by wild-type tumor suppressor gene product p53. Oncogene. 1998;16(18):2395–401. doi:https://doi.org/10.1038/sj.onc.1201742.PubMedView ArticleGoogle Scholar
- Lee DF, Su J, Kim HS, Chang B, Papatsenko D, Zhao R, et al. Modeling familial cancer with induced pluripotent stem cells. Cell. 2015;161(2):240–54. doi:https://doi.org/10.1016/j.cell.2015.02.045.PubMedView ArticleGoogle Scholar
- Park IY, Sohn BH, Choo JH, Joe CO, Seong JK, Lee YI, et al. Deregulation of DNA methyltransferases and loss of parental methylation at the insulin-like growth factor II (Igf2)/H19 loci in p53 knockout mice prior to tumor development. J Cell Biochem. 2005;94(3):585–96. doi:https://doi.org/10.1002/jcb.20263.PubMedView ArticleGoogle Scholar
- Matouk IJ, Mezan S, Mizrahi A, Ohana P, Abu-Lail R, Fellig Y, et al. The oncofetal H19 RNA connection: hypoxia, p53 and cancer. Biochim Biophys Acta. 2010;1803(4):443–51. doi:https://doi.org/10.1016/j.bbamcr.2010.01.010.PubMedView ArticleGoogle Scholar
- Liu C, Chen Z, Fang J, Xu A, Zhang W, Wang Z. H19-derived miR-675 contributes to bladder cancer cell proliferation by regulating p53 activation. Tumour Biol. 2015. doi:https://doi.org/10.1007/s13277-015-3779-2.
- Balmain A. Cancer genetics: from Boveri and Mendel to microarrays. Nat Rev Cancer. 2001;1(1):77–82. doi:https://doi.org/10.1038/35094086.PubMedView ArticleGoogle Scholar
- Davoli T, de Lange T. The causes and consequences of polyploidy in normal development and cancer. Annu Rev Cell Dev Biol. 2011;27:585–610. doi:https://doi.org/10.1146/annurev-cellbio-092910-154234.PubMedView ArticleGoogle Scholar
- Kops GJ, Weaver BA, Cleveland DW. On the road to cancer: aneuploidy and the mitotic checkpoint. Nat Rev Cancer. 2005;5(10):773–85. doi:https://doi.org/10.1038/nrc1714.PubMedView ArticleGoogle Scholar
- Anatskaya OV, Vinogradov AE. Somatic polyploidy promotes cell function under stress and energy depletion: evidence from tissue-specific mammal transcriptome. Funct Integr Genomics. 2010;10(4):433–46. doi:https://doi.org/10.1007/s10142-010-0180-5.PubMedView ArticleGoogle Scholar
- Schoenfelder KP, Fox DT. The expanding implications of polyploidy. J Cell Biol. 2015;209(4):485–91. doi:https://doi.org/10.1083/jcb.201502016.PubMedPubMed CentralView ArticleGoogle Scholar
- Luoto KR, Kumareswaran R, Bristow RG. Tumor hypoxia as a driving force in genetic instability. Genome Integrity. 2013;4(1):5. doi:https://doi.org/10.1186/2041-9414-4-5.PubMed CentralPubMedView ArticleGoogle Scholar
- Storchova Z, Pellman D. From polyploidy to aneuploidy, genome instability and cancer. Nat Rev Mol Cell Biol. 2004;5(1):45–54. doi:https://doi.org/10.1038/nrm1276.PubMedView ArticleGoogle Scholar
- Beroukhim R, Mermel CH, Porter D, Wei G, Raychaudhuri S, Donovan J, et al. The landscape of somatic copy-number alteration across human cancers. Nature. 2010;463(7283):899–905. doi:https://doi.org/10.1038/nature08822.PubMed CentralPubMedView ArticleGoogle Scholar
- Weaver BA, Cleveland DW. Does aneuploidy cause cancer? Curr Opin Cell Biol. 2006;18(6):658–67. doi:https://doi.org/10.1016/j.ceb.2006.10.002.PubMedView ArticleGoogle Scholar
- Vinogradov AE, Anatskaya OV, Kudryavtsev BN. Relationship of hepatocyte ploidy levels with body size and growth rate in mammals. Genome/National Research Council Canada =. Genome/Conseil national de recherches Canada. 2001;44(3):350–60.Google Scholar
- Mosieniak G, Sikora E. Polyploidy: the link between senescence and cancer. Curr Pharm Des. 2010;16(6):734–40.PubMedView ArticleGoogle Scholar
- Coward J, Harding A. Size Does Matter: Why Polyploid Tumor Cells are Critical Drug Targets in the War on Cancer. Frontiers Oncol. 2014;4:123. doi:https://doi.org/10.3389/fonc.2014.00123.View ArticleGoogle Scholar
- Shoshani O, Massalha H, Shani N, Kagan S, Ravid O, Madar S, et al. Polyploidization of murine mesenchymal cells is associated with suppression of the long noncoding RNA H19 and reduced tumorigenicity. Cancer Res. 2012;72(24):6403–13. doi:https://doi.org/10.1158/0008-5472.CAN-12-1155.PubMedView ArticleGoogle Scholar
- Ravid O, Shoshani O, Sela M, Weinstock A, Sadan TW, Gur E, et al. Relative genomic stability of adipose tissue derived mesenchymal stem cells: analysis of ploidy, H19 long non-coding RNA and p53 activity. Stem Cell Res Ther. 2014;5(6):139. doi:https://doi.org/10.1186/scrt529.PubMed CentralPubMedView ArticleGoogle Scholar
- Tsujimoto H, Nishizuka S, Redpath JL, Stanbridge EJ. Differential gene expression in tumorigenic and nontumorigenic HeLa x normal human fibroblast hybrid cells. Mol Carcinog. 1999;26(4):298–304.PubMedView ArticleGoogle Scholar
- Hernandez JM, Elahi A, Clark CW, Wang J, Humphries LA, Centeno B, et al. miR-675 mediates downregulation of Twist1 and Rb in AFP-secreting hepatocellular carcinoma. Ann Surg Oncol. 2013;20 Suppl 3:S625–35. doi:https://doi.org/10.1245/s10434-013-3106-3.PubMedView ArticleGoogle Scholar
- Novak Kujundzic R, Grbesa I, Ivkic M, Katdare M, Gall-Troselj K. Curcumin downregulates H19 gene transcription in tumor cells. J Cell Biochem. 2008;104(5):1781–92. doi:https://doi.org/10.1002/jcb.21742.PubMedView ArticleGoogle Scholar
- Wolanin K, Magalska A, Mosieniak G, Klinger R, McKenna S, Vejda S, et al. Curcumin affects components of the chromosomal passenger complex and induces mitotic catastrophe in apoptosis-resistant Bcr-Abl-expressing cells. Mol Cancer Res. 2006;4(7):457–69. doi:https://doi.org/10.1158/1541-7786.MCR-05-0172.PubMedView ArticleGoogle Scholar
- Shani Nir SO, Zipori Dov. The tissue specific nature of mesenchymal stem/stromal cells: gaining better understanding for improved clinical outcomes. RNA Dis. 2015;2:e780. doi:https://doi.org/10.14800/rd.780.
- Matouk IJ, Raveh E, Abu-lail R, Mezan S, Gilon M, Gershtain E, et al. Oncofetal H19 RNA promotes tumor metastasis. Biochim Biophys Acta. 2014;1843(7):1414–26. doi:https://doi.org/10.1016/j.bbamcr.2014.03.023.PubMedView ArticleGoogle Scholar
- Celton-Morizur S, Merlen G, Couton D, Margall-Ducos G, Desdouets C. The insulin/Akt pathway controls a specific cell division program that leads to generation of binucleated tetraploid liver cells in rodents. J Clin Invest. 2009;119(7):1880–7.PubMed CentralPubMedGoogle Scholar
- Wang G, Lunardi A, Zhang J, Chen Z, Ala U, Webster KA, et al. Zbtb7a suppresses prostate cancer through repression of a Sox9-dependent pathway for cellular senescence bypass and tumor invasion. Nat Genet. 2013;45(7):739–46. doi:https://doi.org/10.1038/ng.2654.PubMed CentralPubMedView ArticleGoogle Scholar
- Cully M, You H, Levine AJ, Mak TW. Beyond PTEN mutations: the PI3K pathway as an integrator of multiple inputs during tumorigenesis. Nat Rev Cancer. 2006;6(3):184–92. doi:https://doi.org/10.1038/nrc1819.PubMedView ArticleGoogle Scholar
- Wesierska-Gadek J, Ranftler C, Schmid G. Physiological ageing: role of p53 and PARP-1 tumor suppressors in the regulation of terminal senescence. J Physiol Pharmacol. 2005;56 Suppl 2:77–88.PubMedGoogle Scholar
- Ogino H, Nozaki T, Gunji A, Maeda M, Suzuki H, Ohta T, et al. Loss of Parp-1 affects gene expression profile in a genome-wide manner in ES cells and liver cells. BMC Genomics. 2007;8:41. doi:https://doi.org/10.1186/1471-2164-8-41.PubMed CentralPubMedView ArticleGoogle Scholar
- Halappanavar SS, Shah GM. Defective control of mitotic and post-mitotic checkpoints in poly(ADP-ribose) polymerase-1(−/−) fibroblasts after mitotic spindle disruption. Cell Cycle. 2004;3(3):335–42.PubMedView ArticleGoogle Scholar
- Tomasetti C, Vogelstein B. Cancer etiology. Variation in cancer risk among tissues can be explained by the number of stem cell divisions. Science. 2015;347(6217):78–81. doi:https://doi.org/10.1126/science.1260825.PubMedPubMed CentralView ArticleGoogle Scholar
- Cunningham ML. Role of increased DNA replication in the carcinogenic risk of nonmutagenic chemical carcinogens. Mutat Res. 1996;365(1–3):59–69.PubMedView ArticleGoogle Scholar
- Vaupel P, Harrison L. Tumor hypoxia: causative factors, compensatory mechanisms, and cellular response. Oncologist. 2004;9 Suppl 5:4–9. doi:https://doi.org/10.1634/theoncologist.9-90005-4.PubMedView ArticleGoogle Scholar
- Vaupel P, Mayer A. Hypoxia in cancer: significance and impact on clinical outcome. Cancer Metastasis Rev. 2007;26(2):225–39. doi:https://doi.org/10.1007/s10555-007-9055-1.PubMedView ArticleGoogle Scholar
- Vaupel P, Mayer A. Hypoxia in tumors: pathogenesis-related classification, characterization of hypoxia subtypes, and associated biological and clinical implications. Adv Exp Med Biol. 2014;812:19–24. doi:https://doi.org/10.1007/978-1-4939-0620-8_3.PubMedView ArticleGoogle Scholar
- Walsh JC, Lebedev A, Aten E, Madsen K, Marciano L, Kolb HC. The clinical importance of assessing tumor hypoxia: relationship of tumor hypoxia to prognosis and therapeutic opportunities. Antioxid Redox Signal. 2014;21(10):1516–54. doi:https://doi.org/10.1089/ars.2013.5378.PubMed CentralPubMedView ArticleGoogle Scholar
- Matouk IJ, DeGroot N, Mezan S, Ayesh S, Abu-lail R, Hochberg A, et al. The H19 non-coding RNA is essential for human tumor growth. PLoS One. 2007;2(9):e845. doi:https://doi.org/10.1371/journal.pone.0000845.PubMed CentralPubMedView ArticleGoogle Scholar
- Ayesh S, Matouk I, Schneider T, Ohana P, Laster M, Al-Sharef W, et al. Possible physiological role of H19 RNA. Mol Carcinog. 2002;35(2):63–74. doi:https://doi.org/10.1002/mc.10075.PubMedView ArticleGoogle Scholar
- Hoogsteen IJ, Marres HA, van der Kogel AJ, Kaanders JH. The hypoxic tumour microenvironment, patient selection and hypoxia-modifying treatments. Clin Oncol (R Coll Radiol). 2007;19(6):385–96. doi:https://doi.org/10.1016/j.clon.2007.03.001.View ArticleGoogle Scholar
- Lottin S, Vercoutter-Edouart AS, Adriaenssens E, Czeszak X, Lemoine J, Roudbaraki M, et al. Thioredoxin post-transcriptional regulation by H19 provides a new function to mRNA-like non-coding RNA. Oncogene. 2002;21(10):1625–31. doi:https://doi.org/10.1038/sj.onc.1205233.PubMedView ArticleGoogle Scholar
- Arner ES, Holmgren A. The thioredoxin system in cancer. Semin Cancer Biol. 2006;16(6):420–6. doi:https://doi.org/10.1016/j.semcancer.2006.10.009.PubMedView ArticleGoogle Scholar
- Luo M, Li Z, Wang W, Zeng Y, Liu Z, Qiu J. Upregulated H19 contributes to bladder cancer cell proliferation by regulating ID2 expression. FEBS J. 2013;280(7):1709–16. doi:https://doi.org/10.1111/febs.12185.PubMedView ArticleGoogle Scholar
- Borras C, Esteve JM, Vina JR, Sastre J, Vina J, Pallardo FV. Glutathione regulates telomerase activity in 3 T3 fibroblasts. J Biol Chem. 2004;279(33):34332–5. doi:https://doi.org/10.1074/jbc.M402425200.PubMedView ArticleGoogle Scholar
- Berteaux N, Lottin S, Monte D, Pinte S, Quatannens B, Coll J, et al. H19 mRNA-like noncoding RNA promotes breast cancer cell proliferation through positive control by E2F1. J Biol Chem. 2005;280(33):29625–36. doi:https://doi.org/10.1074/jbc.M504033200.PubMedView ArticleGoogle Scholar
- Lottin S, Adriaenssens E, Dupressoir T, Berteaux N, Montpellier C, Coll J, et al. Overexpression of an ectopic H19 gene enhances the tumorigenic properties of breast cancer cells. Carcinogenesis. 2002;23(11):1885–95.PubMedView ArticleGoogle Scholar
- Vennin C, Dahmani F, Spruyt N, Adriaenssens E. Role of long non-coding RNA in cells: Example of the H19/IGF2 locus. Adv Biosci Biotechnol. 2013;04(05):11. doi:https://doi.org/10.4236/abb.2013.45A004.Google Scholar
- Valastyan S, Weinberg RA. Tumor metastasis: molecular insights and evolving paradigms. Cell. 2011;147(2):275–92. doi:https://doi.org/10.1016/j.cell.2011.09.024.PubMed CentralPubMedView ArticleGoogle Scholar
- Vanharanta S, Massague J. Origins of metastatic traits. Cancer Cell. 2013;24(4):410–21. doi:https://doi.org/10.1016/j.ccr.2013.09.007.PubMed CentralPubMedView ArticleGoogle Scholar
- Chen H, Paradies NE, Fedor-Chaiken M, Brackenbury R. E-cadherin mediates adhesion and suppresses cell motility via distinct mechanisms. J Cell Sci. 1997;110(Pt 3):345–56.PubMedGoogle Scholar
- Yang J, Mani SA, Donaher JL, Ramaswamy S, Itzykson RA, Come C, et al. Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis. Cell. 2004;117(7):927–39. doi:https://doi.org/10.1016/j.cell.2004.06.006.PubMedView ArticleGoogle Scholar
- Chang CJ, Hung MC. The role of EZH2 in tumour progression. Br J Cancer. 2012;106(2):243–7. doi:https://doi.org/10.1038/bjc.2011.551.PubMed CentralPubMedView ArticleGoogle Scholar
- Ma C, Nong K, Zhu H, Wang W, Huang X, Yuan Z, et al. H19 promotes pancreatic cancer metastasis by derepressing let-7’s suppression on its target HMGA2-mediated EMT. Tumour Biol. 2014;35(9):9163–9. doi:https://doi.org/10.1007/s13277-014-2185-5.PubMedView ArticleGoogle Scholar
- Yan L, Zhou J, Gao Y, Ghazal S, Lu L, Bellone S, et al. Regulation of tumor cell migration and invasion by the H19/let-7 axis is antagonized by metformin-induced DNA methylation. Oncogene. 2014. doi:https://doi.org/10.1038/onc.2014.236.Google Scholar
- Wolfer A, Ramaswamy S. MYC and metastasis. Cancer Res. 2011;71(6):2034–7. doi:https://doi.org/10.1158/0008-5472.CAN-10-3776.PubMed CentralPubMedView ArticleGoogle Scholar
- Wolfer A, Ramaswamy S. Prognostic signatures, cancer metastasis and MYC. Cell Cycle. 2010;9(18):3639. doi:https://doi.org/10.4161/cc.9.18.13220.PubMedView ArticleGoogle Scholar
- Barsyte-Lovejoy D, Lau SK, Boutros PC, Khosravi F, Jurisica I, Andrulis IL, et al. The c-Myc oncogene directly induces the H19 noncoding RNA by allele-specific binding to potentiate tumorigenesis. Cancer Res. 2006;66(10):5330–7. doi:https://doi.org/10.1158/0008-5472.CAN-06-0037.PubMedView ArticleGoogle Scholar
- Gao Y, Wu F, Zhou J, Yan L, Jurczak MJ, Lee HY, et al. The H19/let-7 double-negative feedback loop contributes to glucose metabolism in muscle cells. Nucleic Acids Res. 2014;42(22):13799–811. doi:https://doi.org/10.1093/nar/gku1160.PubMed CentralPubMedView ArticleGoogle Scholar
- Gong L, Goswami S, Giacomini KM, Altman RB, Klein TE. Metformin pathways: pharmacokinetics and pharmacodynamics. Pharmacogenet Genomics. 2012;22(11):820–7. doi:https://doi.org/10.1097/FPC.0b013e3283559b22.PubMed CentralPubMedView ArticleGoogle Scholar
- Milligan L, Antoine E, Bisbal C, Weber M, Brunel C, Forne T, et al. H19 gene expression is up-regulated exclusively by stabilization of the RNA during muscle cell differentiation. Oncogene. 2000;19(50):5810–6. doi:https://doi.org/10.1038/sj.onc.1203965.PubMedView ArticleGoogle Scholar
- Wang L, Wang Y, Li Z, Yu B. Differential expression of long noncoding ribonucleic acids during osteogenic differentiation of human bone marrow mesenchymal stem cells. Int Orthop. 2015;39(5):1013–9. doi:https://doi.org/10.1007/s00264-015-2683-0.PubMedView ArticleGoogle Scholar
- Brabletz T. To differentiate or not--routes towards metastasis. Nat Rev Cancer. 2012;12(6):425–36. doi:https://doi.org/10.1038/nrc3265.PubMedView ArticleGoogle Scholar
- Venkatraman A, He XC, Thorvaldsen JL, Sugimura R, Perry JM, Tao F, et al. Maternal imprinting at the H19-Igf2 locus maintains adult haematopoietic stem cell quiescence. Nature. 2013;500(7462):345–9. doi:https://doi.org/10.1038/nature12303.PubMed CentralPubMedView ArticleGoogle Scholar
- Bauderlique-Le Roy H, Vennin C, Brocqueville G, Spruyt N, Adriaenssens E, Bourette RP. Enrichment of Human Stem-Like Prostate Cells with s-SHIP Promoter Activity Uncovers a Role in Stemness for the Long Noncoding RNA H19. Stem Cells Dev. 2015;24(10):1252–62. doi:https://doi.org/10.1089/scd.2014.0386.PubMedView ArticleGoogle Scholar
- Gabory A, Ripoche MA, Le Digarcher A, Watrin F, Ziyyat A, Forne T, et al. H19 acts as a trans regulator of the imprinted gene network controlling growth in mice. Development. 2009;136(20):3413–21. doi:https://doi.org/10.1242/dev.036061.PubMedView ArticleGoogle Scholar
- Gabory A, Jammes H, Dandolo L. The H19 locus: role of an imprinted non-coding RNA in growth and development. Bioessays. 2010;32(6):473–80. doi:https://doi.org/10.1002/bies.200900170.PubMedView ArticleGoogle Scholar
- Hao Y, Crenshaw T, Moulton T, Newcomb E, Tycko B. Tumour-suppressor activity of H19 RNA. Nature. 1993;365(6448):764–7. doi:https://doi.org/10.1038/365764a0.PubMedView ArticleGoogle Scholar
- Yoshimizu T, Miroglio A, Ripoche MA, Gabory A, Vernucci M, Riccio A, et al. The H19 locus acts in vivo as a tumor suppressor. Proc Natl Acad Sci U S A. 2008;105(34):12417–22. doi:https://doi.org/10.1073/pnas.0801540105.PubMed CentralPubMedView ArticleGoogle Scholar
- Garibaldi F, Cicchini C, Conigliaro A, Santangelo L, Cozzolino AM, Grassi G, et al. An epistatic mini-circuitry between the transcription factors Snail and HNF4alpha controls liver stem cell and hepatocyte features exhorting opposite regulation on stemness-inhibiting microRNAs. Cell Death Differ. 2012;19(6):937–46. doi:https://doi.org/10.1038/cdd.2011.175.PubMed CentralPubMedView ArticleGoogle Scholar
- Zhang L, Yang F, Yuan JH, Yuan SX, Zhou WP, Huo XS, et al. Epigenetic activation of the MiR-200 family contributes to H19-mediated metastasis suppression in hepatocellular carcinoma. Carcinogenesis. 2013;34(3):577–86. doi:https://doi.org/10.1093/carcin/bgs381.PubMedView ArticleGoogle Scholar
- Dykxhoorn DM, Wu Y, Xie H, Yu F, Lal A, Petrocca F, et al. miR-200 enhances mouse breast cancer cell colonization to form distant metastases. PLoS One. 2009;4(9):e7181. doi:https://doi.org/10.1371/journal.pone.0007181.PubMed CentralPubMedView ArticleGoogle Scholar
- Santangelo L, Marchetti A, Cicchini C, Conigliaro A, Conti B, Mancone C, et al. The stable repression of mesenchymal program is required for hepatocyte identity: a novel role for hepatocyte nuclear factor 4alpha. Hepatology. 2011;53(6):2063–74. doi:https://doi.org/10.1002/hep.24280.PubMedView ArticleGoogle Scholar
- Alder O, Cullum R, Lee S, Kan AC, Wei W, Yi Y, et al. Hippo signaling influences HNF4A and FOXA2 enhancer switching during hepatocyte differentiation. Cell Reports. 2014;9(1):261–71. doi:https://doi.org/10.1016/j.celrep.2014.08.046.PubMed CentralPubMedView ArticleGoogle Scholar
- Lamar JM, Stern P, Liu H, Schindler JW, Jiang ZG, Hynes RO. The Hippo pathway target, YAP, promotes metastasis through its TEAD-interaction domain. Proc Natl Acad Sci U S A. 2012;109(37):E2441–50. doi:https://doi.org/10.1073/pnas.1212021109.PubMed CentralPubMedView ArticleGoogle Scholar
- Chan LH, Wang W, Yeung W, Deng Y, Yuan P, Mak KK. Hedgehog signaling induces osteosarcoma development through Yap1 and H19 overexpression. Oncogene. 2014;33(40):4857–66. doi:https://doi.org/10.1038/onc.2013.433.PubMedView ArticleGoogle Scholar
- Gregory PA, Bert AG, Paterson EL, Barry SC, Tsykin A, Farshid G, et al. The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1. Nat Cell Biol. 2008;10(5):593–601. doi:https://doi.org/10.1038/ncb1722.PubMedView ArticleGoogle Scholar
- Hill L, Browne G, Tulchinsky E. ZEB/miR-200 feedback loop: at the crossroads of signal transduction in cancer. Int J Cancer. 2013;132(4):745–54. doi:https://doi.org/10.1002/ijc.27708.PubMedView ArticleGoogle Scholar
- Fernandez LA, Northcott PA, Dalton J, Fraga C, Ellison D, Angers S, et al. YAP1 is amplified and up-regulated in hedgehog-associated medulloblastomas and mediates Sonic hedgehog-driven neural precursor proliferation. Genes Dev. 2009;23(23):2729–41. doi:https://doi.org/10.1101/gad.1824509.View ArticleGoogle Scholar
- Kiesslich T, Pichler M, Neureiter D. Epigenetic control of epithelial-mesenchymal-transition in human cancer. Mol Clin Oncol. 2013;1(1):3–11. doi:https://doi.org/10.3892/mco.2012.28.PubMed CentralPubMedGoogle Scholar
- Berteaux N, Aptel N, Cathala G, Genton C, Coll J, Daccache A, et al. A novel H19 antisense RNA overexpressed in breast cancer contributes to paternal IGF2 expression. Mol Cell Biol. 2008;28(22):6731–45. doi:https://doi.org/10.1128/MCB.02103-07.PubMed CentralPubMedView ArticleGoogle Scholar
- Tran VG, Court F, Duputie A, Antoine E, Aptel N, Milligan L, et al. H19 antisense RNA can up-regulate Igf2 transcription by activation of a novel promoter in mouse myoblasts. PLoS One. 2012;7(5):e37923. doi:https://doi.org/10.1371/journal.pone.0037923.PubMed CentralPubMedView ArticleGoogle Scholar
- Onyango P, Feinberg AP. A nucleolar protein, H19 opposite tumor suppressor (HOTS), is a tumor growth inhibitor encoded by a human imprinted H19 antisense transcript. Proc Natl Acad Sci U S A. 2011;108(40):16759–64. doi:https://doi.org/10.1073/pnas.1110904108.PubMed CentralPubMedView ArticleGoogle Scholar