- Open Access
miR-375 activates p21 and suppresses telomerase activity by coordinately regulating HPV E6/E7, E6AP, CIP2A, and 14-3-3ζ
Molecular Cancer volume 13, Article number: 80 (2014)
While microRNAs (miRNAs) are extensively studied in post-transcriptional regulation of gene expressions in many biological processes, cellular miRNA-mediated regulation of viral genes remains unclear. In particular, the interplay between human papillomavirus (HPV) genes and miRNAs and how these interactions contribute to HPV-associated cancers remain elusive.
Transient transfection of miR-375-mimic was used to compensate the loss-of-function of miR-375 in HPV-positive cancer. Regulation of oncogenic molecules and their downstream molecules via miR-375 in HPV-positive cancer was investigated using qRT-PCR, western blot, dual luciferase assay, indirect immunofluorescence analysis. All experiments were conducted at least three times to achieve statistical significance determined by Student t-test.
In this study, we demonstrated how miR-375 negatively regulates HPV16 and 18 transcripts. We also found a cellular protein, E6-associated protein (E6AP), directly regulated by miR-375. miR-375-mediated repression of HPV transcripts and E6AP elevated major tumor suppressors p53, p21, and retinoblastoma protein 1 (RB). Cooperative regulation of miR-375 targets along with the increase of tumor suppressors led to ~60% reduction of telomerase reverse transcriptase (TERT) transcription followed by ~35% decrease of telomerase activity. Furthermore, miR-375-mediated regulation of 14-3-3ζ contributes to decrease telomerase activity by altering nuclear translocation of TERT.
Taken together, miR-375-mediated suppression of multiple oncogenic components in HPV-associated carcinogenesis generates a cumulative biological response to rescue key tumor suppressors and diminish telomerase activity, which results in cell cycle arrest and cell proliferation inhibition.
MicroRNAs (miRNAs) are approximately 22 nucleotide (nt) long small non-coding RNAs that play key roles in differentiation and development by post-transcriptional regulation of cellular genes. Although typical miRNA-mRNA interactions occur in the 3′ untranslated region (UTR) of the target, coding sequences are also subjected to miRNA binding. This binding directs translational repression and mRNA degradation[2, 3]. Over 1,000 human miRNAs are predicted to regulate approximately 60% of protein-coding genes, indicating their extensive functions in many biological processes.
Human papillomaviruses (HPVs) are 8-kb double-stranded DNA viruses that specifically target basal cells of the epithelial mucosa. HPV infection is implicated in virtually all cervical cancers, ~90% of anal cancers, 30 ~ 60% of oropharyngeal cancers, and ~40% of vaginal, vulvar, and penile cancers. HPV16 and HPV18 are the most common HPV types associated with these aforementioned cancers. High-risk HPVs closely linked to malignancies have developed strategies to evade the human immune system. Examples include suppressing interferon-α-inducible gene expression[8, 9], and directly regulating interferon signaling pathways by HPV E6/E7[10, 11]. While little is known about the role of E1 in HPV-mediated cancers, E6 and E7 coded by high-risk HPVs are considered highly oncogenic[5, 7, 12–15].
Telomeres are specialized functional complexes that maintain the integrity and stability of the genome by protecting the ends of eukaryotic chromosomes. A telomere consists of hexanucleotide (TTAGGG) tandem repeats, ending with a single stranded overhang that forms telosomes with protein complexes. In normally dividing somatic cells, telomeres shorten by about 60-150 bp with each cell division due to the DNA end replication problem[18, 19]. Then telomeres are shortened to a certain length, cell cycle arrest and proliferation failure occur, inducing cellular senescence. Tumors can overcome this regulation by activating telomerase, a ribonucleoprotein complex enzyme with reverse transcriptase activity that maintains a constant telomere length[21, 22]. Enhanced telomerase activity is observed in most malignant tumors (~90%) but the mechanisms underlying its regulation are not fully understood.
In the present study, we showed that miR-375 suppresses high-risk HPV E6 and E7, and E6AP. Moreover, the effect of these regulations was incorporated with previous findings of miR-375 targets shown in other cancer cells[3, 24]. This study demonstrates how miR-375 behaves as a tumor suppressor miRNA by rescuing major tumor suppressors, suppressing oncogenic components, and thus regulates cell cycle and telomerase activity.
miR-375 targets HPV type 16 and 18 transcripts and suppresses E6 and E7 expression
While searching for oncogenic targets regulated by miR-375 in addition to cancerous Inhibitor of PP2A (CIP2A) in our previous study, we investigated potential interactions between miR-375 and HPV16 transcripts. We used the program RNA22 to predict these potential interactions because this algorithm relies on sequence complementarity between miRNA and target RNA regardless of interaction location within the transcript. A total of five putative miR-375 binding sites were predicted, two in the E7 region and three in the E1 region (Figure 1A). We generated FL reporter constructs to determine the direct interactions between miR-375 and these predicted sites. We inserted E7/E1 region downstream of the FL reporter (Figure 1B). Site-directed mutagenesis generated mutations in the seed sequences of five miR-375 binding sites (Figure 1A and1B). Co-transfection of FL-E7/E1 reporter with miR-375-mimic showed 25-30% repression, and the repression effect was abolished when the five miRNA-mRNA interactions were disrupted (FL-E7/E1-m1-5, Figure 1B). Co-transfection of FL-E7 with miR-375-mimic resulted in ~20% reduced FL activity, but mutation of individual binding sites (m1 or m2) did not rescue this repression effect (Additional file1: Figure S1A). Similar results were observed when FL-E1 was co-transfected with miR-375-mimic. FL activity was significantly reduced (~20%) by miR-375 but mutations on single miR-375 binding sites (m3 to m5) did not rescue this repression (Additional file1: Figure S1B). These results indicate that the five binding sites more likely produce a synergistic effect, instead of an additive effect, to suppress HPV16 transcript expression.
In order to measure the repression effect of miR-375 on endogenous HPV16 transcripts, two HPV16-positive cancer cell lines, cervical cancer line SiHa and oropharyngeal cancer line UPCI:SCC090 (hereafter SCC090), were transfected with miR-375-mimic. E6 and E7 mRNA expression were measured 48 h post-transfection using Taqman quantitative PCR. Interestingly, both E6 and E7 transcript levels were reduced ~60% in SiHa cells transfected with 25 nM of miR-375-mimic molecules (Figure 1C). In SCC090 cells, neither 50 nor 100 nM of miR-375-mimic was sufficient to reduce E6 or E7 levels. Significant reduction of both E6 and E7 (~30%) was observed when a higher concentration (200 nM) of miR-375-mimic was used for transfection (Figure 1D). This higher dose requirement in SCC090 cells could be explained by the dramatically higher HPV16 transcript levels present compared to SiHa cells (Additional file1: Figure S2). E6, E7, and E6/E7/E1 transcripts were detected in both cell lines, as well as in three human oropharyngeal tumors (T1-T3) (Additional file1: Figure S2). Although four E6 mRNA splicing isoforms were detected as reported previously, the miR-375-mediated repression observed here is not affected since the putative miR-375 binding sites are located on E7 and E1 region. Interestingly, miR-375-mimic transfection in HeLa cells (HPV18 positive) also reduced both E6 and E7 transcript levels by ~50% (Figure 1E). Bioinformatics suggested that HPV18 also have putative binding sites for miR-375 (data not shown). Transfection of miR-375 inhibitor did not affect the expression of HPV16 and HPV18 transcript expressions in SiHa, SCC090, and HeLa cells because endogenous miR-375 levels in these cells were already extremely low (~32 Ct values by real-time PCR). However, the functionality of the miR-375 inhibitor was clearly demonstrated in the transfection of MCF7 cells which had moderate expression of miR-375 (see in the following figures). Taken together, these data indicate that miR-375 directly regulates HPV16 and HPV18 transcripts.
miR-375 directly targets and represses E6AP
Prediction of miR-375 binding site in the E6AP 3′UTR was performed by TargetScan. The 3′UTR of E6AP was cloned downstream of FL reporter and site-directed mutagenesis of four nucleotides in the seed binding sites was also generated to test the putative miRNA-mRNA interaction (Figure 2A). The dual luciferase reporter system was used to investigate the direct interaction between E6AP 3′UTR and miR-375. A significant decrease in FL activity (30%, p <0.01) was observed. This direct repression effect was abolished by mutating the seed binding site (Figure 2B). SiHa cells were used in the following experiments as HPV16-positive cells due to the lower concentration of miR-375-mimic required for HPV16 suppression in SiHa compared to SCC090 cells (Figure 1). Transfection of miR-375-mimic (25 nM) in SiHa cells reduced ~50% of E6AP protein levels (Figure 2C) and ~30% of endogenous E6AP mRNA (Figure 2D). Transfection of miR-375-mimic (25 nM) in HeLa cells reduced ~30% of E6AP protein and ~40% of E6AP mRNA (Figure 2E and2F). These results demonstrate that miR-375 directly regulates E6AP by interacting with the 3′UTR.
miR-375 increases p21, p53, and RB in HPV16- and 18-positive cancer
HPV-positive cervical or oropharyngeal cancers contain wild type p53 and/or RB, and inactivation of these tumor suppressors are driven by E6 and E7 proteins produced from high-risk HPVs[28–30]. Cellular E6AP forms a complex with E6, inhibiting p53 by ubiquitin-dependent degradation. E7 degrades RB, activating cell proliferation genes[32, 33]. Therefore, SiHa and HeLa cells are appropriate representative model systems for studying HPV16 and HPV18, because they are known to contain wild type p53 and RB, respectively. To examine the downstream effect of miR-375-mediated regulation of HPV transcripts and E6AP, we examined the expression of crucial tumor suppressors related to these pathways. In SiHa cells, miR-375-mimic transfection increased p53 and RB protein levels (Figure 3A). Interestingly, p21, which is a major downstream player in p53-mediated tumor suppression, showed dramatic protein level elevation after miR-375-mimic transfection (Figure 3A). p21 transcript levels significantly increased in cells with miR-375-mimic transfection (Figure 3B) and this increase could be explained by p53 protein level elevation (Figure 3A). The increase of p53 and RB proteins was not a result of transcriptional activation of corresponding genes, which indicates minimal changes in de novo proteins (Figure 3B). Therefore, it is more reasonable to interpret the increase as rescue of p53 and RB proteins by the miR-375-mediated suppression of E6 and E7 (Figure 1). A significant decrease in cell proliferation (~50%) was observed after miR-375-mimic transfection, compared to cells transfected with NS control (Figure 3C). These results showed that the rescue of tumor suppressors by miR-375-mediated regulation of E6 and E7 viral oncoproteins led to reduced proliferation of HPV-positive cancer cells.
Similar results were observed in HeLa cells. p21, p53, and RB protein levels dramatically increased and p21 mRNA levels significantly elevated in HeLa cells 48 h post-transfection of miR-375-mimic (Figure 3D and3E). We observed about 40% reduction of cell proliferation after 48 h (Figure 3F). p21, p53, and RB are important cell cycle regulators[34–36]. Thus, flow cytometry was used to measure the cellular DNA content of cells transfected with miR-375-mimic or inhibitor to determine the cell cycle status. We observed a dramatic increase in G1-arrested cells and a reduced amount of S and G2/M phase cells 48 h post-transfection of miR-375-mimic, compared to NS control (~23%, p < 0.001, Figure 3G). Together, these results explain how miR-375 inhibits proliferation of these HPV-positive cancer cells.
miR-375 control on CIP2A-MYC pathway also contributes to p21 elevation
In our previous study, we identified CIP2A as a target of miR-375 in oral cancer. CIP2A protects MYC from dephosphorylation by PP2A and as a result prevents its proteolytic degradation, and MYC is a transcriptional repressor of p21. Thus, the potential involvement of miR-375 regulation of CIP2A-MYC in this pathway was investigated. We used siRNAs to knockdown either CIP2A or p53 to examine to effects of these proteins on p21 expression. Knockdown of p53 dramatically reduced p21 protein levels (76% reduction, Figure 3H). We also found a potential relevance between CIP2A and p53. Silencing CIP2A led to 33% increase of p53 (Figure 3H) and knockdown of p53 increased CIP2A to 40-80% (Figure 3H and3I). While how p53 regulates CIP2A is unknown, it is clear that CIP2A plays a protective role for MYC, and that MYC impairs transactivation of p53 in human cancer cells[39–41]. Interestingly, knockdown of CIP2A increased p21 by 69% (Figure 3H), and increase of p21 by CIP2A silencing was also observed in p53-knockdown cells (a slight increase from 24% to 33%, Figure 3H). This result indicated that induction of p21 by miR-375 is mainly due to the elevation of its major transcriptional activator p53, and miR-375-mediated reduction of its transcriptional repressor MYC also contributes to p21 increase.
The effect of miR-375-mimic was examined in p53-knockdown SiHa cells in order to validate the contribution of CIP2A-MYC in miR-375-mediated increase in p21. Consistent with our previous observation, CIP2A was suppressed by miR-375 in SiHa cells (21% reduction, Figure 3I). Despite the variation in the increases of p53 and p21 shown in Figure 3A and3I, the miR-375-mediated induction of p53 and p21 was reproducible in these separated experimental conditions. The reduced elevation shown in Figure 3I, compared to Figure 3A, may be affected by the co-transfection with si-GFP. Importantly, when miR-375-mimic was transfected into p53-knockdown cells, there was a dramatic increase of p21 (increase from 14% to 41%, Figure 3I). Since si-p53 efficiently silenced p53 proteins to a barely detectable level, miR-375-mediated increase of p21 is regulated by alternative pathways besides the major transactivator p53 (Figure 3I). Transcripts of p21 were significantly elevated by miR-375, as well as in p53-knockdown cells (Figure 3J). This indicates that in addition to p53-mediated activation of p21, miR-375 can activate p21 by regulating its suppressor MYC in the absence of p53.
miR-375 increases p21 expression by inducing p53 and suppressing CIP2A-MYC
We selected MCF7 as an HPV-negative model system to compare functional differences of miR-375 in HPV-positive versus HPV-negative cells. It is advantageous to use MCF7 cells because they are known to carry wild type p53 and RB[42, 43]. This information allows us to rule out potential unexpected consequences that mutations in p53 and RB would generate. The same set of proteins that were examined in SiHa cells (p21, p53, and RB) were analyzed in MCF7 cells after transfecting miR-375 inhibitor, -mimic, or NS control (Figure 4A). Interestingly, transfection of miR-375-mimic did not change p53 and RB protein levels, compared to NS control transfected MCF7 cells. In contrast, p21 protein levels increased in miR-375-mimic transfected cells by 197% (Figure 4A). Despite the decrease of E6AP in miR-375-mimic transfected MCF7 cells (31% compared to NS control, data not shown), p53 protein level remained unaffected (Figure 4A). This finding confirms that miR-375-mediated suppression of E6 is required for p53 elevation. A significant increase of p21 transcripts was also observed in miR-375-mimic transfected MCF7 cells (120% compared to NS control, Figure 4B), although these fold changes were not as dramatic as those shown in HPV-positive cells (SiHa, ~330%, Figure 3B; HeLa, 350%, Figure 3E). MCF7 cells have relatively higher level of endogenous miR-375 (~27 Ct values by real-time PCR) than SiHa or HeLa cells. As a result, unlike no change observed in HPV-positive cells (Figure 3) with low miR-375 levels, transfection of miR-375 inhibitor in MCF7 cells decreased the level of p21 mRNA indicating that suppressing miR-375 led to repression of p21 (Figure 4B). Because p53 protein levels were not induced by miR-375-mimic transfection, an alternative explanation is required to explain the apparent increase of p21 transcriptional activation by miR-375 in MCF7 cells.
As described in our previous study, we confirmed that miR-375 suppressed CIP2A expression in MCF7 cells. About 40% and 70% reduction of CIP2A and MYC protein levels, respectively, were observed in miR-375-mimic transfected MCF7 cells, compared to NS control transfection (Figure 4A). This reduction indicates functional regulation of these molecules by miR-375 in this cell line. siRNA-mediated silencing of CIP2A causes degradation of MYC[3, 37]. Using this strategy, CIP2A knockdown resulted in MYC reduction and p21 elevation in a siRNA dose-dependent manner (Figure 4C). Transfection of miR-375-mimic in p53-knockdown MCF7 cells increased the protein expression of p53 and p21 (Figure 4D) as well as p21 transcription (Figure 4E). The moderate increase of p53 shown in Figure 4D (compare lane 3 and 4, 9% versus 30%) indicated the potential of an HPV-independent pathway to activate p53. Since a miRNA can regulate multiple targets, this observation would require further investigation to fully understand how miR-375 induced p53 in HPV-negative cancer cells. Nevertheless, together with the results in Figure 3, these data suggested that replenishment of miR-375 can reactivate the expression of p21 through rescue of p53 from HPV E6, and miR-375-mediated suppression of CIP2A-MYC also contributes to the rescue of p21 in HPV-positive cancer cells. Although an increased percentage of G1 phase cells were observed in miR-375-mimic transfected cells compared to NS control (~10%, p < 0.001), this increase was not dramatic as that shown in SiHa cells (compare Figure 3G and4F). Since MCF7 cells contained relatively higher level of miR-375 than SiHa cells, miR-375 inhibitor transfection showed reduction of G1 phase cells.
Collectively, miR-375 mediates co-regulation of CIP2A, E6, E6AP, and E7, and rescues the expression of major tumor suppressors p21, p53, and RB. Given the fact that p53 and MYC cross regulates each other[39–41, 44], it is important to note that activation of p53 and suppression of MYC can be cooperated by miR-375, and results in activation of p21. As a consequence, activation of these tumor suppressors inhibit cell cycle progression and suppresses HPV-positive cancer cell proliferation (Figure 4G).
miR-375-mediated repression of HPV16 E6, E6AP, and CIP2A activates p53-RB-p21 network and suppresses telomerase activity
Because our data suggested that the absence of miR-375 in HPV-positive cancer cells leads to uncontrolled expression of miR-375 targets (HPV transcripts, E6AP, and CIP2A) and downstream molecules (p53, p21, RB, and MYC), we used siRNAs to silence individual miR-375 targets and examined their relative importance. Semiquantitative analyses of CIP2A, E6, and E6AP silencing by specific siRNA were conducted using two different siRNA concentrations (1 and 10 nM, Figure 5A). The effect of miR-375 was also examined using two different miR-375-mimic concentrations (5 and 50 nM) for parallel comparison. Due to the lack of an efficient antibody for E6 protein detection, its known target, p53, was quantitated as an E6 functional surrogate. Compared to si-GFP transfected cells, miR-375 transfection with two different siRNA concentrations confirmed the decrease of CIP2A and E6AP and the increase of p53 and p21 (Figure 5A). Individual siRNA transfection (si-CIP2A, si-E6, and si-E6AP) increased both p53 and p21 protein levels in concentration-dependent manners. Combination of three siRNAs (si-Three) showed an effect similar to using miR-375-mimic to reduce CIP2A and E6AP and elevate p53 and p21 (Figure 5A). Despite some technical difficulties in comparing the efficiency of each siRNA, silencing individual components of this pathway exclusively led to transcriptional activation of p21, as demonstrated in p21 mRNA analysis (Figure 5B). This data demonstrated that miR-375 increases p21 transcription possibly by coordinated regulation of CIP2A, HPV E6, and E6AP in this HPV-positive cancer cell.
Interestingly, proteins involved in the aforementioned pathways are well-known regulatory molecules for telomerase activity. MYC and E6 are transcriptional activators of TERT, while p53, p21, and RB are transcriptional repressors of TERT[46–49]. Therefore, we hypothesized that miR-375-mediated coordinated regulation of these components may lead to TERT transcriptional regulation. CIP2A knockdown alone was not sufficient to regulate TERT transcription, but silencing E6 or E6AP reduced TERT transcripts in SiHa cells (37% and 41% reduction, respectively, Figure 5C). Downregulation of the TERT transcript was most prominent when three siRNAs were used together compared to si-GFP control (57% reduction, p < 0.0001) and miR-375 exerted comparable or an even stronger reduction (~63% reduction, p < 0.0001, Figure 5C). The telomeric repeat amplification protocol assay incorporated with SYBR real-time PCR was used to measure telomerase activities in SiHa cells transfected with miR-375-mimic or inhibitor. About 35% reduced activity was observed in miR-375-mimic transfected cells whereas miR-375 inhibitor exhibited an opposite effect showing ~20% increase (Figure 5D). Taken together, this data shows miR-375 could regulate overall telomerase activity by reducing TERT transcription via CIP2A, E6, and/or E6AP in SiHa cells.
miR-375 modulates TERT nuclear translocation by regulating 14-3-3ζ
14-3-3 proteins interact with a wide variety of proteins involved in regulating many cellular processes. 14-3-3 protein isoforms θ and ζ inhibit CRM1/exportin-1 binding of the TERT nuclear export signal motif. These isoforms share a conserved C-terminal domain that binds TERT and enhances TERT nuclear localization. Interestingly, 14-3-3ζ has been identified as a miR-375 target. We confirmed that miR-375-mimic represses 14-3-3ζ mRNA and protein levels ~50% in HeLa cells (Figure 6A and6B). This data suggests the possibility that miR-375-mediated repression of 14-3-3ζ may affect the nuclear localization of TERT. 14-3-3ζ and TERT localization was examined by indirect immunofluorescence of HeLa cells transfected with miR-375-mimic or inhibitor. Overall fluorescence intensity for 14-3-3ζ was reduced in miR-375-mimic transfected cells compared to untreated cells and cells transfected with miR-375 inhibitors (Figure 6C). This result was expected as miR-375 inhibited de novo protein synthesis (Figure 6B). Comparing the ratio of 14-3-3ζ nuclear/cytoplasmic localization in untreated cells, miR-375-mimic transfected cells, and miR-375 inhibitor transfected cells, untreated and miR-375-mimic transfected cells had minimal differences (~10%) while miR-375 inhibitor treated cells demonstrated a dramatic increase (~300%) in this ratio (Figure 6D). This prominent decrease in cytoplasmic 14-3-3ζ expression could explain the slight increase of the nuclear/cytoplasmic ratio of 14-3-3ζ in miR-375-mimic transfected cells compared to untreated cells. Similarly, minimal changes in TERT nuclear localization were observed in miR-375-mimic transfected cells (12% decrease) and miR-375 inhibitor transfection enhanced nuclear localization of TERT (190% increase, Figure 6C and6E). These results indicate that miR-375 modulates nuclear localization of 14-3-3ζ and TERT.
Here we show the importance of miR-375 as a master suppressor of multiple oncogenic components involved in HPV-associated carcinogenesis. Repression mediated via a single miRNA has modest inhibitory effects on hundreds of targets (typically less than two-fold), but the strength of miRNA to change the gene-regulatory network comes from the cumulative reduction of multiple components of a pathway that enables miRNA to elicit biological changes[52–54]. Our results clearly show how miR-375 simultaneously coordinates regulation of HPV E6/E7, E6AP, and CIP2A to inhibit TERT transcription, and represses 14-3-3ζ to block TERT nuclear localization. Importantly, replenishment of miR-375 causes repression of these targets and rescues the major tumor suppressor network p53-p21-RB which is also involved in transcriptional repression of TERT. As a consequence, in the presence of miR-375, cell cycle arrest, telomerase inactivation, and proliferation inhibition maintain cellular homeostasis (Figure 7).
The loss of miR-375 is important for development of several types of cancers such as oral cancer, head and neck cancer[55–58], cervical cancer, hepatocellular cancer, oesophageal cancer, and gastric cancer[24, 62]. Our study shows that low expression of miR-375 in HPV-associated cancers also contribute to carcinogenesis promoted by high-risk HPVs. Replenishment of miR-375 in HPV-positive cervical cancer cell lines and oropharyngeal cell line significantly reduces the levels of HPV transcripts. Moreover, miR-375 plays important role in regulating E6AP which is a protein required for HPV-mediated p53 degradation. It is important to note the oncogenic properties of high-risk HPVs. E6 and E7 can degrade important tumor suppressors p53, p21, and RB, and promote cellular machinery dysfunction required for homeostasis[33, 63]. E6, in conjunction with cellular protein E6AP, targets p53 and leads to its proteosomal degradation. p53 degradation inhibits p53-mediated apoptosis, reduces p21-mediated cell cycle regulation, and destabilizes chromosomes[64–66]. E7 oncoprotein binds and degrades RB via ubiquitin-mediated degradation. RB degradation releases E2F, promoting transcriptional activation of many cell proliferation genes. E7 protein also inactivates p21 and disrupts cell cycle control of normal human epithelial cells. Therefore, our finding is that miR-375 critically suppresses HPV E6 and E7 expression, and as a result, maintains regular expressions of tumor suppressor genes in these epithelial cells.
HPV produces polycistronic mRNAs that contain E6, E7, and E1 regions and alternative splicing on HPV polycistronic transcripts is important for E6 and E7 oncoprotein expressions. Unspliced E6 coding region is essential for full-length E6 protein production. However, splicing on E6 region that prevents full-length E6 from being expressed and elevates E7 expression[68, 69]. It has been suggested that alternative splicing of E6/E7 transcripts of high-risk HPVs occurs depending on epithelial growth factor (EGF). In the presence of EGF, equivalent amount of E6 and another isoform E6*I are produced, whereas E6*I expression becomes dominant in EGF depleted condition. Splicing events may occur during differentiation where EGF and EGF receptor levels change during differentiation of suprabasal epithelial cells. While it is clear that alternative splicing of HPV transcripts have functional relevance on biological processes such as cell cycle and differentiation, miR-375-mediated regulation of HPV transcripts are not affected by alternative splicing because the putative miR-375 binding sites are located either on E7 or E1 region and not on E6 region. Since the primers and probes used for the real time qPCR analyses of E6 or E7 transcript are located in regions that are common in all spliced transcripts, our data support that miR-375-mediated regulation of HPV transcripts will be independent of E6 mRNA splicing as long as the transcripts have downstream E7 and E1 regions still in place.
Our work on miR-375 adds to the growing body of evidence implicating the association between miRNA and HPV in cancers. Previous studies have shown the influence of HPV genes on miRNA expressions. For example, HPV16 E6 modulates miR-218 levels and E6-mediated degradation p53 leads to suppression of miR-34a, miR-23b, and miR-145. E7 protein downregulates miR-203 upon differentiation of suprabasal epithelial cells. These observations are not surprising because E6 and E7 modulate numbers of major transcription factors such as MYC, p53, and E2F which are upstream molecules for a large number of these miRNA genes. MYC induces expression of miR-17-92 family, and represses a number of miRNAs including miR-30 family. p53 not only transcriptionally activates miR-34a but also regulates biogenesis of mature miR-15a, miR-16-1, miR-23a, miR-26a, miR-103, miR-143, miR-145, miR-203, and miR-206. p53 also function as transcriptional repressor mediated by E2F to modulate miRNA expressions. Previous studies suggest a potential of miRNAs involved in HPV regulation by showing that high levels of miR-203 in differentiating suprabasal cells have inhibitory effect on HPV amplification and miR-125b interaction with late gene of HPV6. These reports indicate a high possibility for other miRNA-mediated regulation for HPV transcripts but experimental validation is still needed. Therefore, our finding that a single cellular miRNA regulates HPV transcripts suggests a need for a systemic investigation to unveil cellular miRNA-mediated direct and/or indirect regulations of HPV genes. Our cell culture system used HPV-positive cancer cell lines that express endogenous HPV viral genes, and this system has limitation to mimic the natural HPV infections in epithelial cells since HPVs do not replicate in cell culture. Therefore, additional investigations are required to understand whether sufficient endogenous miR-375 levels in epithelial cells can suppress HPV viral gene expressions by using organotypic (raft) tissue culture system that mimic fully differentiated epithelium[82, 83].
Our study showed mechanistically for the first time how cellular miRNA interacts with high-risk HPV transcripts and reduces their expression. Present data demonstrated that supplement of miR-375 in HPV-positive cancer cells coordinates the regulation of HPV E6/E7, E6AP, CIP2A, and 14-3-3ζ, which secures the expression of tumor suppressors p53, RB, and p21, and regulates telomerase activity. Therefore, loss of miR-375 during HPV-mediated carcinogenesis is likely to lead mis-regulation of this network. Our current finding suggests a need of development of therapeutic approaches to increase miR-375 levels in HPV-associated cancers, which will suppress oncoproteins but in turn re-express major tumor suppressors and ultimately lead to improve clinical outcomes.
Materials and methods
Patient specimens, cell culture, and transfection
Three oropharyngeal tumors were obtained from the Tissue Bank at the Moffitt Cancer Center (protocol no. MCC-15370) and approved by the Institutional Review Board of the University of South Florida (no. 106444). SiHa, HEK293, and HeLa cells were cultured as described in previous publication, and MCF7 cells were cultured in DMEM supplemented with 10% fetal bovine serum, 100 μg/mL streptomycin, and 100 U/mL penicillin. UPCI:SCC090 is an HPV16-positive tongue cancer cell line provided from Dr. Susanne Gollin at the University of Pittsburgh. Transfection was performed using Lipofectamine 2000. Sequences of siRNAs were designed according to previous reports: CIP2A, 5′- CUGUGGUUGUGUUUGCACUdTdT-3′; HPV16 E6, 5′-ACCGTTGTGTGATTTGTTAdTdT-3′; E6AP, 5′-CAACTCCTGCTCTGAGATAdTdT-3′. siRNAs were synthesized from Thermo Fisher Scientific (Waltham, MA). p53 siRNA was purchased from Thermo Fisher Scientific (D003329-05-0002). GFP siRNA (Thermo Fisher Scientific, D-001300-01-20) was used as a control.
Western blot and antibodies
Western blotting was performed and analyzed as described. Primary antibodies used were mouse anti-MYC (9E-10, Santa Cruz Biotechnology), mouse monoclonal anti-CIP2A (2G10, Novus Biologicals), rabbit anti-E6AP (H-182, Santa Cruz Biotechnology), mouse anti-p53 (DO-1, Santa Cruz Biotechnology), rabbit anti-RB1 (10048-2-Ig, Proteintech), rabbit anti-p21 (10355-1-AP, Proteintech), rabbit anti-14-3-3ζ (C-16, Santa Cruz Biotechnology), and mouse anti-tubulin (Sigma-Aldrich).
Dual luciferase assay and site-directed mutagenesis
The luciferase assay was performed in HEK293 cells using the dual luciferase reporter assay system (Promega) and analyzed as described. cDNA fragments of HPV16 transcript and E6AP 3′UTR were subcloned into a pMiR-Target vector between EcoR I and Not I restriction enzyme sites downstream of Firefly luciferase (FL) coding sequence (OriGene Technologies, Rockville, MD). Four nucleotides in the seed binding sites were mutated to disrupt the miRNA-mRNA interaction as described previously. Renilla luciferase reporter was used to normalize the data. All primers used for cloning luciferase construction and mutagenesis are listed in Additional file1: Table S1.
Cell cycle analysis by flow cytometry
SiHa and MCF7 cells were harvested 48 h post-transfection and cellular DNA content was measured using Cycletest Plus DNA Reagent Kit (BD Biosciences, San Jose, CA). Samples were analyzed on a FACS Calibur flow cytometer (BD Biosciences) and the data was collected using Cell Quest Software, Version 3.3 (BD Biosciences). Flow cytometry measured the fluorescence from propidium iodide as an indication of DNA content during cell cycle. Fluorescence was excited by a 15 mW laser emitting at 488 nm. Emission was collected using a 585 nm +/- 21 nm bandpass filter. Data for 2×104 events were collected per sample. Cell cycle analysis was performed using Modfit software, version 3.1 (Verity Software House, Topsham, ME).
Real-time quantitative telomeric repeat amplification protocol (RQ-TRAP) assay and TaqMan qRT-PCR
TaqMan qRT-PCR was performed as described[3, 87]. Customized primers and probes for detection of E6 and E7 from HPV16 or HPV18 were selected from a published report: HPV16 E6-F, 5′- GCACCAAAAGAGAACTGCAATGTT-3′; HPV16 E6-R, 5′-AGTCATATACCTCACGTCGCAGTA-3′; HPV16 E6-probe, 5′-GGACCCACAGGAGCGACCCAGAAAGTTA-3′; HPV16 E7-F, 5′-CAAGTGTGACTCTACGCTTCGG-3′; HPV16 E7-R, 5′-GTGGCCCATTAACAGGTCTTCCAA-3′; HPV16 E7-probe, 5′-TGCGTACAAAGCACACACGTAGACATTCGT-3′; HPV18 E6-F, 5′-CTATAGAGGCCAGTGCCATTCG-3′; HPV18 E6-R, 5′-TTATACTTGTGTTTCTCTGCGTCG-3′; HPV18 E6-probe, 5′-CAACCGAGCACGACAGGAACGACTCCA-3′; HPV18 E7-F, 5′-TAATCATCAACATTTACCAGCCCG-3′; HPV18 E7-R, 5′-CGTCTGCTGAGCTTTCTACTACTA-3′; HPV18 E7-probe, 5′-CGAGCCGAACCACAACGTCACACAATGTT-3′. Semi-quantitative PCR detected full length HPV16 transcripts of E6, E7, and E6/E7/E1. HPV16 E6-F1, 5′-ATGCACCAAAAGAGAACTGC-3′; HPV16 E6-R1, 5′-TTACAGCTGGGTTTCTCTACG-3′; HPV16 E7-F1, 5′-ATGCATGGAGATACACCTACA-3′; HPV16 E7-R1, 5′-TTATGGTTTCTGACAACAGATGG-3′. E6/E7/E1 gene product was detected using HPV16 E6-F1 and E1 reverse cloning primer described in Additional file1: Table S1. E6 isoforms were clearly detected in the tumors and cell lines in our study (Additional file1: Figure S2). Telomerase activity was detected using TRAPeze Telomerase Detection Kit (Millipore) combined with SYBR green real-time PCR. Briefly, cells were resuspended in CHAPS lysis buffer, incubated on ice for 30 min and obtained the supernatant after centrifuging at 12,000 g for 20 min at 4°C. Heat-inactivated samples were incubated at 85°C for 10 min and were used to normalize the total telomerase activity. SYBR green real-time and TaqMan qRT-PCR were performed using the Applied Biosystems StepOne Real-Time PCR machine.
Indirect immunofluorescence and quantification of fluorescence
Indirect immunofluorescence was performed as described[3, 90, 91] using rabbit anti-14-3-3ζ and rabbit anti-TERT. Alexa 568 goat anti-rabbit Ig were used as secondary antibodies. Images were taken at ×400 magnification using Zeiss Axiovert 200 M microscope. Fluorescence intensities in the nuclear and cytoplasmic regions were quantified using ImageJ (http://rsbweb.nih.gov/ij/). Nuclear/Cytoplasmic ratios were calculated from the mean of fluorescence intensities measured in a defined circular area within the nucleus or cytoplasm of each cell. Twenty cells were captured and ratios calculated for quantification.
Experiments were conducted at least trice, and data are shown as mean ± SD. Statistical analyses for miR-375-mimic transfected samples were performed by comparing the values of NS control transfected samples unless indicated in figures. Statistical analyses were performed using two-tailed Student’s t test using GraphPad Prism 4.0 (Graph Pad Software, La Jolla, CA).
Written informed consent was obtained from patients for the publication of this report.
Retinoblastoma protein 1
Telomerase reverse transcriptase
3′ untranslated region
Cancerous Inhibitor of PP2A.
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We thank S. John Calise in the Chan lab for technical assistance and encouragement. We thank Neal Benson at the UF Interdisciplinary Center for Biotechnology Research for assistance with cell cycle analysis. We also thank Susanne M. Gollin at the University of Pittsburgh for providing UPCI:SCC090 cells. This work was supported by the Alumni Graduate Fellowship (HMJ), Andrew J. Semesco Foundation (HMJ, EKLC), and UF/ Moffitt Collaborative Initiative grant (EKLC).
The authors declare that they have no competing interests.
HMJ and EKLC designed research and analyzed data. HMJ and BLP carried out experiments. HMJ and EKLC wrote the paper. All authors have read and approved the final manuscript.
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Additional file 1: Figure S1: Mutation of single miR-375 binding site does not abolish the repression effect. PCR amplification of E6, E7, and E6E7E1 transcripts in SiHa, SCC090, and three HPV16 positive oropharyngeal tumors (T1-T3). Table S1. Primer sequences for cloning and mutagenesis. (PDF 411 KB)
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Jung, H.M., Phillips, B.L. & Chan, E.K. miR-375 activates p21 and suppresses telomerase activity by coordinately regulating HPV E6/E7, E6AP, CIP2A, and 14-3-3ζ. Mol Cancer 13, 80 (2014). https://doi.org/10.1186/1476-4598-13-80
- Human papillomavirus