MicroRNA‑106a inhibits cell proliferation and induces apoptosis in colorectal cancer cells
- Authors:
- Published online on: April 17, 2018 https://doi.org/10.3892/ol.2018.8516
- Pages: 8941-8944
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Copyright: © Huang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Each year, >1 million new cases of colorectal cancer (CRC) are diagnosed worldwide. CRC is the third most common malignancy and the fourth most common cause of cancer-associated mortality (1). Despite novel biological insights and advances in therapy, the prognosis of patients with CRC remains poor. The molecular mechanisms underlying malignant tumor occurrence and progression was investigated, with the aim of developing more effective therapies against CRC.
MicroRNAs (miRNAs) are a group of endogenous small noncoding RNAs that are 21–25 nucleotides in size. The primary function of miRNA is to suppress gene expression, either by inhibiting mRNA translation or inducing mRNA degradation (2). It is estimated that miRNAs regulate the expression of >60% of human protein-encoding genes (3), and are involved in modulating multiple cellular pathways, including cell proliferation, differentiation and apoptosis (4). miRNAs can serve as tumor suppressors or oncogenes, depending on their target mRNAs, and their expression can in turn be regulated by tumor suppressors (5) and oncogenes (6,7). Aberrant expression of certain miRNAs has been observed in an array of human cancer types, and miRNAs are thought to serve important roles in tumorigenesis. Recently, a number of miRNAs have been identified as oncogenes or tumor suppressor genes in CRC (8–12).
miR-106a is expressed in cancer cells and in stool samples of patients with CRC with varying degrees (13–15). However, the molecular role that miR-106a serves in CRC remains debatable. Thus, in the present study, the biological consequence of overexpressing miR-106a in two distinct CRC cell lines was investigated.
Materials and methods
Cell lines and cultures
Human CRC cell lines HCT116 and SW620 were obtained from the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). Cells were maintained in RPMI-1640 with 10% fetal bovine serum (both from Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA) and 1% antibiotics (100 U/ml penicillin and 100 µg/ml streptomycin sulfate) in a humidified atmosphere containing 5% CO2 at 37°C.
miRNA mimics and transfections
miR-106a mimics and nontarget control were purchased from Shanghai GenePharma Co., Ltd. (Shanghai, China). The sequences of these synthetic miRNAs were as follows: miR-106a mimic forward, 5′-AAAAGUGCUUACAGUGCAGGUAG-3′ and reverse, 5′-ACCUGCACUGUAAGCACUUUUUU-3′; nontarget control forward, 5′-UUCUCCGAACGUGUCACGUTT-3′ and reverse, 5′-ACGUGACACGUUCGGAGAATT-3′. Cells were transfected with the miRNA (100 nM/l) using Lipofectamine™ 2000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) following manufacturer's protocol.
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)
Total RNA from cells was extracted using TRIzol (Invitrogen; Thermo Fisher Scientific, Inc.) according to manufacturer's protocol. First-strand cDNA synthesis was performed using the TaqMan MicroRNA Reverse Transcription kit and miR-106a RT primers (Applied Biosystems; Thermo Fisher Scientific, Inc.). The temperature protocol of first-strand cDNA synthesis was: 16°C for 30 min, 42°C for 30 min and 85°C for 5 min. qPCR was performed using a miR-106a TaqMan MicroRNA Assay and TaqMan Universal Master Mix II on an ABI PRISM 7500 (Applied Biosystems; Thermo Fisher Scientific, Inc.). miR-106a primer sequence: GGAAAAGTGCTTACAGTGCAGGTAG. Thermocycler conditions used as follow: 95°C for 5 min, followed by 40 cycles at 95°C for 30 sec, 55°C for 40 sec and 72°C for 30 sec. The expression of miR-106a was normalized to that of U6 (U6-forward primer: 5′-GTCGTATCCAGTGCAGGGTCCGAGGT-3′; U6-reverse primer: 5′-GCACTGGATACGACAAAATATGGAAC-3′). Data analysis was performed using the 2−ΔΔCq method (16).
Cell proliferation assay
Cell proliferation was measured using a Cell Counting Kit-8 (CCK-8) assay (Beyotime Institute of Biotechnology, Haimen, China) according to manufacturer's protocol. Briefly, cells were plated in 96-well plates at a density of 0.5×104 cells/well. CCK-8 (10 µl) was added to each well prior to the colorimetric measurement. After 1 h incubation at 37°C, the absorbance at 450 nm was measured using a microplate luminometer reader.
Cell apoptosis assay
Apoptosis assays were performed using an Annexin V apoptosis detection kit according to the manufacturer's protocol (BD Biosciences, San Jose, CA, USA). Briefly, CRC cells were collected after 72 h transfection, washed with PBS and resuspended in binding buffer containing 10 mM HEPES (pH 7.4), 2.5 mM CaCl2, and 140 mM NaCl. Annexin V-PE and 7-AAD were then added and flow cytometry analysis was performed after 15 min of incubation at room temperature.
Immunoblotting
Total protein was extracted using whole cell lysis buffer (Beyotime Institute of Biotechnology). Immunoblotting was performed as previously described (13). The following antibodies were used: 1, Anti-E2F transcription factor 1 (E2F1) (1:1,000; Cell Signaling Technology, Inc., Danvers, MA, USA); 2, anti-caspase-9 antibodies (1:3,000; Cell Signaling Technology, Inc.); 3, anti-GAPDH antibodies (1:10,000; Zhongshan Goldenbridge Biotechnology, Guangzhou, China). The membrane was washed with Tris-buffered saline with Tween-20 and incubated with a peroxidase-conjugated secondary antibody (1:1,000; Santa Cruz Biotechnology) for 1 h. Protein bands were visualized using enhanced chemiluminesence substrates (EMD Millipore, Billerica, MA, USA).
Statistical analysis
Data are expressed as the mean ± standard deviation and were analyzed using SPSS 13.0 software (SPSS Inc., Chicago, IL, USA). One-way analysis of variance was used for comparing multiple groups, followed with the Student-Newman-Keuls post hoc test. P<0.05 was considered to indicate a statistically significant difference. All experiments were performed in biological triplicates.
Results
miR-106a overexpression inhibits the proliferation of colorectal cancer cells in vitro
The effect of miR-106a expression on the proliferation of CRC cells was examined first. HCT116 and SW620 cells were transiently transfected with nontarget control or miR-106a mimics. The RT-qPCR results demonstrated that cells transfected with miR-106a mimics exhibited a significantly higher level of miR-106a compared with cells transfected with a nontarget control miRNA or with mock transfection (Fig. 1A). In addition, cells overexpressing miR-106a mimics revealed a significant decrease in the cell proliferation rate 48 and 72 h after transfection (Fig. 1B).
miR-106a overexpression enhances apoptosis of colorectal cancer cells in vitro
Whether miR-106a overexpression induces apoptosis of CRC cells was examined next. Cells transfected with miR-106a or controls were stained with Annexin V and 7-AAD to measure cell apoptosis 72 h after transfection. miR-106a mimics caused significant increases in the percentage of apoptotic cells (HCT116: miR-106a, 16.69±0.82 vs. nontarget control, 8.38±1.86%; SW620: miR-106a, 12.44±0.97 1 vs. nontarget control, 5.77±0.21%), while no significant difference was identified between the blank and nontarget control group (Fig. 1C and D).
miR-106a overexpression causes a marked change in the expression of E2F1 and cleaved caspase-9
Immunoblot analysis revealed that the protein level of E2F1 was decreased following miR-106a overexpression. Furthermore, caspase-9 cleavage was examined upon miR-106a overexpression and it was demonstrated that active caspase-9 was significantly enhanced compared with control cells (Fig. 1E).
Discussion
miRNAs have been demonstrated to serve essential roles in carcinogenesis (17–21). Aberrant expression of certain miRNAs has been implicated in a variety of tumor properties, including growth, carcinogenesis, angiogenesis and apoptosis. The role of miR-106a serves in the malignant progression of tumors is complex and controversial. Numerous studies have revealed that miR-106a may serve as a tumor suppressor or an oncogene in different cancer types, which may be dependent on the cellular context (22,23). For example, miR-106a exerts a tumor suppressive effect via suppressing proliferation and inducing apoptosis in human glioma cells by targeting E2F1, regardless of p53 status (22). In breasts cancer, miR-106a enhances cell proliferation and migration by negatively regulating zinc-finger and BTB domain containing 4 (23). However, the role of miR-106a in CRC carcinogenesis remains unclear.
The present work identified miR-106a as a tumor-suppressive miRNA in CRC cells in vitro. Overexpression of miR-106a induced apoptosis and decreased proliferation in CRC cells. The oncogene E2F1, target gene of miR-106a was decreased following miR-106a overexpression while apoptosis was elicited. Simultaneously, caspase-9 expression, an important caspase in the apoptotic pathway, was induced. Once active, caspase-9 triggers a cascade of caspase activation events leading to apoptosis.
Collectively, the results of the current study demonstrated that miR-106a may serve as a tumor suppressor in CRC, potentially through regulating E2F1 and caspase-9 expression in cultured cancer cells. However, in vivo studies are warranted to validate these findings.
Acknowledgements
The authors would like to thank Dr Dennis Liang Fei of National Institutes of Health (Bethesda, USA) for providing editorial assistance.
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