miR-335 represents an invasion suppressor gene in ovarian cancer by targeting Bcl-w

Introduction

Due to the insidious nature of ovarian cancer, few patients can be diagnosed before the cancer has spread beyond the ovaries, making ovarian cancer the most lethal gynecological malignancy and the fifth leading cause of cancer-related mortality in women worldwide (1,2). Yet, our understanding of the molecular mechanisms that govern its dissemination remains fragmental.

microRNAs (miRNAs) are small, non-coding RNAs with a length of ~22 nucleotides, which negatively regulate gene expression by promoting mRNA cleavage or by translational suppression (3). miR-335 has been found to function as an oncogene or tumor-suppressor in a wide variety of cancers (4). It functions as a tumor-suppressor in breast cancer and inhibits metastasis and migration of breast cancer cells (5). Similarly, miR-335 was found to suppress gastric cancer metastasis in vitro and in vivo(6). Lynch et al(7) also found that miR-335 inhibits the invasive and migratory potential of neuroblastoma cells. Interestingly, miR-335 has been reported to be upregulated in glioma (8), as a putative miRNA oncogene in conferring tumorigenic features such as growth and invasion on malignant astrocytoma cell lines in vitro and could be potently required for differentiation of malignant glioma cell lines (9). These findings suggest that the roles of miR-335 vary based on the type of cancer. It will be necessary to determine the expression status of miR-335 in each type of tumor.

Previous profiling studies have associated miR-335 with ovarian cancer (10–12). However, its expression and biological function in ovarian cancer remain unexplored. A search for miR-335 regulatory targets that may be involved in the progression of ovarian cancer using online prediction algorithms has identified Bcl-w, which harbors a putative miR-335 binding site in its 3′-UTR. Bcl-w is an anti-apoptotic member of the Bcl-2 protein family. It is upregulated in tumors such as gastric, colorectal, cervical and breast cancer (13–15). It can promote cell invasion in gastric cancer (13) and inhibit apoptosis in human colorectal cancers (16). These results suggest that the dependency of cancer cells on overexpressed or activated Bcl-w for various tumor-promoting phenotypes, such as sustained survival, proliferation, invasion and metastasis, may be different among tissues or cell types. In this study, we demonstrated that miR-335 may act as a metastasis suppressor in ovarian cancer by targeting Bcl-w and MMP-2.

Materials and methods

Tissue samples

Samples of human normal ovarian tissues were obtained from patients who underwent surgery at Wuhan Union Hospital from 2004 to 2009. The normal tissues were obtained from patients who underwent wedge biopsy of the ovaries, or adnexectomy due to myoma or adenomyosis. After ovary removal, the germinal epithelium was peeled off and subjected to further analysis. After this, 17 normal ovarian tissues were analyzed. Specimen collection and archiving of patient data were performed upon written informed consent and were approved by the ethics committee of the hospital.

Cell culture and transfection

Human epithelial ovarian cancer cell lines, SKOV3, ES2, A2780 and CAOV3, were purchased from the China Center for Type Culture Collection (Wuhan, China) and were propagated in Dulbecco’s modified Eagle’s medium (DMEM) (Gibco-BRL, Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS) (Gibco-BRL). For miRNA-335 overexpression, SKOV3 and ES2 cells were transfected with miR-335 mimics or a scrambled sequence as miR-control (GenePharma Co., Ltd., Shanghai, China). For Bcl-w overexpression, SKOV3 cells were transfected with Bcl-w expression constructs, which had been rendered insensitive to miR-335 by deletion of its 3′UTR (GenePharma Co., Ltd.). All transfections were performed using Lipofectamine™ 2000 reagent (Invitrogen Life Technologies, Carlsbad, CA, USA) according to the manufacturer’s protocols.

RNA extraction and real-time PCR analysis

Total RNA was extracted with TRIzol reagent (Invitrogen Life Technologies). The expression level of miR-335 was analyzed using the Hairpin-it™ miRNAs qPCR Quantitation kit (GenePharma, Co. Ltd.), following the manufacturer’s instructions. U6 was used as the reference gene for normalization.

For determination of Bcl-w expression levels, reverse transcription was run using RevertAid™ First Strand cDNA synthesis kit (MBI Fermentas, Flamborough, ON, Canada) according to the supplied protocol. The 25 μl polymerase chain reaction (PCR) mixture included 2X SYBR-Green qPCR master mix (Toyobo, Japan), 2.5 μl of cDNA template and 0.3 μM of each primer. Primers for Bcl-w were as follows: forward, 5′-GAGCCATATAGTTCCTTGGGA-3′ and reverse, 5′-TAGAATAAGTGGGGAGTGGGA-3; and for β-actin, forward, 5′-GCCAACACAGTGCTGTCTGG-3′ and reverse, 5′-GCTCAGGAGGAGCAATGATCTTG-3′. β-actin was used as a reference gene for normalization. The expression of each gene was defined from the threshold cycle (Ct), and relative expression levels were calculated using the 2−ΔΔCT method. All reactions were run in triplicate.

Cell proliferation analysis

Cell proliferation was measured by detecting incorporation of 5-ethynyl-2′-deoxyuridine (EdU) during DNA synthesis using Clik-iT® EdU Imaging kit (Invitrogen Life Technologies) with minor modifications to the manufacturer’s protocol. Briefly, cells that had been propagated in a 96-well plate for 48 h were exposed to 10 μM of EdU for 4 h. After EdU exposure, cells were fixed with 4% formaldehyde and treated with 0.5% Triton X-100. Proliferative cells were visualized using Click-iT® reaction cocktail. Subsequently, cells were counterstained with Hoechst 33342. All assays were carried out in triplicate.

Migration and invasion assays

To evaluate cell migration and invasion, Transwell cell migration and Matrigel invasion assays were carried out according to a previously reported protocol (17). The results are represented as the means of the cell numbers of 10 randomly selected visual fields (x200 magnification). All assays were performed in triplicate. In corroboration with the Transwell cell migration and Matrigel invasion assays, a wound-healing assay was carried out according to a previously reported protocol (18). Percent migration was calculated by measuring the length and width of the cell-free area. The width was measured at five points along the scratch area and then averaged to obtain an accurate representation of the entire scratch area. Percent migration was determined using the following formula: [Δ area/area (day 0)] × 100.

F-actin immunofluorescence

SKOV3 cells were transfected with miR-335 mimics or the miR-control, as described above, and plated onto uncoated glass coverslips in a 12-well plate. The cells were fixed with 4% formaldehyde, permeabilized in 0.1% Triton X-100 and reacted with phallotoxins (Invitrogen Life Technologies) for 60 min. Subsequently, cell nuclei were counterstained with Hoechst 33342. Images were acquired using an 1X71 digital camera (Olympus, Tokyo, Japan).

Bioinformatics

For miRNA target gene prediction, we used TargetScan release 5.1 online software (http://www.targetscan.org/) and PicTac (http://pictar.mdc-berlin.de/).

Protein extraction and western blot analysis

Total cell extracts were resolved on SDS polyacrylamide gels and blotted onto a Hybond PVDF membrane (GE Healthcare, UK). The following antibodies were used: anti-Bcl-w (1:500 dilution; Cell Signaling Technology, Inc., Beverly, MA, USA), anti-β-actin (1:1,000 dilution; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA), anti-MMP-2 (1:1,000 dilution; Vector Laboratories, Burlingame, CA, USA). The antigen-antibody complexes were visualized using horseradish peroxidase-conjugated secondary antibody (1:5,000 dilution; Santa Cruz Biotechnology, Inc.).

Statistical analysis

Data are presented as means ± SD from at least 3 separate experiments. Unless otherwise noted, one-way ANOVA was used for comparisons between groups. All statistical analyses were carried out with SPSS 12.0 computer software (SPSS, Inc., Chicago, IL, USA). P<0.05 was considered to indicate a statistically significant result.

Results

miR-335 is downregulated in ovarian cancer cell lines

To determine whether miR-335 plays a role in the tumorigenesis of epithelial ovarian cancer, we examined its expression in 17 normal ovarian tissue samples using stem-loop quantitative reverse transcription-polymerase chain reaction (RT-PCR). We found that miR-335 expression was reduced in ovarian cancer cell lines in comparison with normal ovarian epithelium (Fig. 1).

Figure 1 Downregulation of miR-335 expression in ovarian cancer cell lines. Relative expression of miR-335 in normal ovarian tissues and cancer cell lines, SKOV3, ES2, A2780, CAOV3, was measured by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) using U6 as the reference gene. Results represent the mean values. Bars, SD. All reactions were run in triplicate. Relative quantification was performed using the 2−ΔΔCT method.

miR-335 suppresses metastasis-relevant traits in vitro

Given that miR-335 is downregulated in ovarian cancer cell lines, we proceeded to explore its impact on relevant biological behavior of ovarian cancer. Since the expression of miR-335 was most significantly reduced in the SKOV3 and ES2 cell lines, we chose these for further study. Thus, we overexpressed miR-335 in SKOV3 and ES2 cell lines by transiently transfecting them with hsa-miR-335 mimics. Ectopic miR-335 did not affect cell proliferation in vitro (Fig. 2A and B), but did reduce the migratory and invasive ability of SKOV3 and ES2 cells (Fig. 2C and D). The effect of miR-335 overexpression on cell migration was further supported by the wound-healing assay (Fig. 2E). Moreover, under a florescence microscope, numerous F-actin bundles were clearly visible in SKOV3 cells transfected with the miR-335 mimics, while control cells contained markedly fewer, finer and shorter bundles and exhibited an elongated morphology with lamellipodia (Fig. 2F), suggesting miR-335 exerts anti-migratory activity in ovarian cancer cells at least partly by inhibiting actin polymerization.

Figure 2 miR-335 suppresses metastasis-relevant traits in vitro. SKOV3 and ES2 cells were transfected with miR-335 mimics or the miR-control. (A) Representative photomicrographs of EdU results for SKOV3 and ES2 cells were captured at ×200 magnification. (B) Mean of EdU triplicate experiments for SKOV3 and ES2; bars, SD. (C) The indicated cell transfectants were seeded onto either uncoated or Matrigel-coated polycarbonate filters to analyze their migratory and invasive potentials. Cells that migrated through the filters were stained and counted under a microscope at ×200 magnification. (D) Mean values of Transwell triplicate experiments for SKOV3 and ES2 cells; bars, SD. (E) SKOV3 cells were seeded in 6-well plates and wounded on the next day. Images were captured under a microscope at ×200 magnification at 0 and 24 h after the wounding. (F) Staining of the F-actin cytoskeleton with phalloidin revealed extensive pseudopodia and lamellipodia (arrows) in SKOV3 cells. The images were captured under ×400 magnification. Nuclei were stained with Hoechst 33342.

miR-335 suppresses the invasiveness of ovarian cancer by targeting Bcl-w and Bcl-w effector, MMP-2

For miRNA target gene prediction, we used TargetScan release 5.1 online software (http://www.targetscan.org/, Whitehead Institute for Biomedical Research, Cambridge, MA, USA). Among a total of 146 genes that was potentially targeted by miR-335, we found that Bcl-w may contribute to the metastasis of ovarian cancer. To establish that miR-335 targets Bcl-w in ovarian cancer, we overexpressed miR-335 in SKOV3 and ES2 cells. We found that ectopic miR-335 significantly repressed Bcl-w protein levels while no difference was detected between the miR-control and untreated cells. Moreover, a concomitant repression of the Bcl-w effector, MMP-2, was also observed (Fig. 3A and B). These observations demonstrated that miR-335 targets Bcl-w in ovarian cancer. In spite of these findings, no reduction in Bcl-w was observed at the mRNA level when miR-335 was modulated in SKOV3 and ES2 cells (Fig. 3C and D).

Figure 3 miR-335 inhibits cell migration and invasion via Bcl-w by decreasing MMP-2 in SKOV3 and ES2 cells. (A and B) The mRNA levels in the indicated SKOV3 and ES2 transfectants were compared using quantitative reverse transcription-polymerase chain reaction (qRT-PCR). (C and D) Cellular levels of Bcl-w and MMP-2 in the indicated SKOV3 and ES2 cell transfectants were compared by western blotting using β-actin as a loading control.

Ectopic Bcl-w reverses miR-335-mediated invasion defects

To establish that the ability of miR-335 to impede cell invasion is mainly mediated by the downregulation of Bcl-w, we concomitantly transfected SKOV3 and ES2 cells with 335 mimics and Bcl-w expression constructs. In these cells, ectopic Bcl-w reversed the miR-335-imposed invasion defects (Fig. 4C and D). Under the same conditions, we observed a significant increase in MMP-2 (Fig. 4A and B).

Figure 4 Ectopic Bcl-w offsets miR-335-mediated invasion. Bcl-w expression vectors were constructed and introduced into SKOV3 and ES2 miR-335 mimic transfectants. (A and B) Cellular levels of Bcl-w and MMP-2 in the indicated SKOV3 and ES2 cell transfectants were compared by western blotting using β-actin as a loading control. (C and D) Top, the migratory and invasive potentials of the co-transfectants were compared with the Bcl-w transfectants and miR-control. Bottom, columns, mean of triplicate experiments; bars, SD.

Discussion

miRNAs can modulate a wide variety of biological processes. In the present report, we demonstrated that a single human miRNA, miR-335, is endowed with the ability to repress the pro-metastatic target, Bcl-w, and thereby to inhibit invasion in ovarian cancer.

To date, only a limited number of miRNAs with pro-metastatic or anti-metastatic functions have been identified in ovarian cancer (19–23), miR-34 has been reported to be endowed with the ability to mitigate invasion (19). miR-21 has been categorized as a pro-metastatic gene (22). However, its specific contributions to metastasis are not easily discerned as they have significant effects on cell proliferation at the same time. In contrast, miR-335 obstructs invasion without exerting confounding influences on cell proliferation. As such, it may aptly be categorized as an ‘exclusive invasion suppressor’.

Bcl-w is an anti-apoptotic member of the Bcl-2 protein family. It suppresses apoptosis by direct interaction with pro-apoptotic members and by blocking their apoptotic activities (24–27), and previous evidence suggests that the expression of Bcl-w is associated with infiltrative morphotypes (14). Recently, reporter gene assays have validated its role as an effector of miR-335 (6). Although mutations in the anti-apoptotic Bcl-2 family members (Bcl-xL, Mcl-1, Bcl-w and A1) have not been identified as a cause of tumors, high expression of these proteins can contribute to carcinogenesis in cooperation with other proto-oncogenes (28). Bcl-w can promote cell invasion by activating the PI3K-Akt-Sp1-MMP-2 pathway (13) and blocking the invasion suppression action of Bax (29). In our research, we demonstrated that miR-335 supressed the invasiveness of ovarian cancer by targeting Bcl-w and Bcl-w effector, MMP-2.

In spite of this, we found that miR-335-mediated defects in invasion could not be fully mitigated by ectopic Bcl-w, and that miR-335 affected actin polymerization, an important step in EMT. Thus, the possibility that miR-335-mediated defects in invasion are achieved by recruiting a cohort of effectors cannot formally be excluded, again highlighting the pleiotropic action of miRNAs.

miRNAs effect gene silencing via both translational repression or mRNA degradation pathways. When an miRNA and its cognate mRNA interact with perfect complementarity, the target mRNA is directly cleaved, resulting in the reduction in the abundance of the target mRNA. However, in animals, miRNAs generally interact with target mRNAs with only partial complementarity. This mode of recognition results in translational repression of the target mRNA with much smaller effects on the level of target mRNA abundance (6,12,15,30). In our study, it was found that ectopic miR-335 significantly reduced Bcl-w expression at the protein level. However, no corresponding decrease in Bcl-w expression was observed at the mRNA level. In fact, such a finding is not unprecedented (19) and is consistent with the notion that mammalian cells favor translational repression.

In summary, our results suggest that decreased miR-335 facilitates ovarian cancer invasion via the Bcl-w pathway. To our knowledge, this represents the first observation of reduced miR-335 expression in human ovarian cancer. Moreover, as metastases are responsible for patient mortality in ovarian cancer, the ability of miR-335 to impede invasion may prove to be clinically useful.

Acknowledgements

We thank the Department of Obstetrics and Gynecology, Union Hospital, Wuhan, Hubei, China, for providing the tissue samples. This study was supported by the Scientific Research Foundation for the Returned Overseas Chinese Scholars, the State Education Ministry.

References