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Introduction

Ovarian cancer is one of the most common human malignancies in females, resulting in a high rate of mortality (1). Extensive efforts have been made to improve treatment; however, the survival rate for patients with chemoresistant ovarian cancer remains low (2–4). It has been reported that certain oncogenes and tumor suppressors are dysregulated and serve critical functions during the development and progression of ovarian cancer, and some of these have been suggested to be promising therapeutic targets or candidates (5,6). Thus, investigations into the functions of these genes appear to be beneficial for developing novel strategies for the treatment of ovarian cancer.

MicroRNAs (miRs), a class of non-coding RNAs 18–25 nucleotides in length, inhibit the expression of their target genes by binding to the 3′-untranslated regions (3′UTRs) of their target mRNAs, inducing mRNA degradation or protein translation inhibition (7,8). It has been well documented that miRs are involved in the regulation of numerous cellular processes, including cell survival, differentiation, proliferation and motility (8–11). Additionally, numerous miRs have been reported to be involved in the malignant phenotypes of cancer cells, including cancer cell proliferation, migration, invasion and chemoresistance, by negatively regulating the expression of oncogenes or tumor suppressors (12–15). miR-142-3p has been indicated to act as a tumor suppressor in several common cancer types (16–18). For instance, the downregulation of miR-142-3p may contribute to thyroid follicular tumorigenesis by targeting ASH1 like histone lysine methyltransferase and histone-lysine-N-methyltransferase 2A (16). However, the underlying mechanism of miR-142-3p in ovarian cancer is yet to be investigated.

Sirtuin 1 (SIRT1) is a member of the sirtuin family of proteins and functions as an intracellular regulatory protein with mono-ADP-ribosyltransferase and deacetylase activity (19). Recently, Shuang et al (20) reported that SIRT1 overexpression contributed to chemoresistance and poor prognosis in serous epithelial ovarian cancer. In addition, Mvunta et al (21) revealed that SIRT1 also promoted ovarian cancer cell invasion. Therefore, SIRT1 functions as an oncogene in ovarian cancer; however, the regulatory mechanism of SIRT1 expression is largely unknown.

The present study aimed to investigate the expression of miR-142-3p in ovarian cancer, as well as the molecular mechanism of miR-142-3p underlying the proliferation and chemoresistance of ovarian cancer cells.

Materials and methods

Tissue collection

The present study was approved by the ethics committee of the First Affiliated Hospital of Xinxiang Medical University (Weihui, China). Ovarian cancer tissues (n=58) and their matched adjacent normal tissues were collected from 58 patients with ovarian cancer from the First Affiliated Hospital of Xinxiang Medical University between September 2014 and April 2016. The patients were between 44 and 68 years old, with a mean age of 57.7 years. Written informed consent was obtained from all patients. No patients received radiation therapy or chemotherapy prior to surgical resection. The tissues were immediately snap-frozen in liquid nitrogen following surgical removal and stored until use. The clinical characteristics of patients, as determined using tumor, node, metastasis staging are summarized in Table I (22). Patients were included in the present study if they exhibited primary ovarian cancer and were excluded if they had received radiation therapy or chemotherapy prior to surgical resection. In addition, all patients involved in the present study were categorized into a high miR-142-3p expression group and a low miR-142-3p expression group, based on the mean expression value (1.16) of miR-142-3p.

Table I. Association between miR-142-3p expression and clinicopathological characteristics of patients with ovarian cancer.

Table I.

Association between miR-142-3p expression and clinicopathological characteristics of patients with ovarian cancer.

Variable	Cases (n=58)	Low miR-142-3p (n=32)	High miR-142-3p (n=26)	P-value
Age, years				0.594
≤55	22	11	11
>55	36	21	15
Differentiation				0.027a
Well/moderately	37	16	21
Poor	21	16	5
Lymph node metastasis				0.156
Present	17	12	5
Absent	41	20	21
Clinical stage				0.113
I–II	33	15	18
III–IV	25	17	8

a P<0.05. miR, microRNA.

Cell culture

Normal human ovarian epithelial cell line IOSE386, human ovarian cancer cell lines (SKOV3, HOC1, HO-8910) and the cisplatin-resistant ovarian cancer cell line SKOV3/DDP cells were purchased from American Type Culture Collection (Manassas, VA, USA). Ovarian cancer OVAC cells were purchased from Cell Bank of Central South University (Changsha, China). The cell lines were cultured in RPMI-1640 (Hyclone; GE Healthcare Life Sciences, Logan, UT, USA) supplemented with 15% fetal bovine serum (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) at 37°C in 5% CO2.

Cell transfection

To study the function of miR-142-3p and SIRT1, SKOV3 and SKOV3/DDP cells were transfected with miR-142-3p mimic (cat. no. B01001), scrambled miR control (cat. no. B01001; miR-NC), negative control (NC) inhibitor (cat. no. B03001; anti-NC), miR-142-3p inhibitor (cat. no. B03001; anti-miR-142-3p; all obtained from Shanghai GenePharma Co., Ltd., Shanghai, China), or co-transfected with miR-142-3p mimic and pcDNA3.1-SIRT1 plasmid (Yearthbio, Changsha, China), or co-transfected with miR-142-3p mimic and blank pcDNA3.1 vector using Lipofectamine® 2000 (Invitrogen; Thermo Fisher Scientific, Inc.), according to the manufacturer's protocol.

Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)

Total RNA from tissues and cell lines was extracted using RNAiso plus (Takara Bio, Inc., Otsu, Japan). RNA was then converted into cDNA on an ABI 7300 plus system (Thermo Fisher Scientific, Inc.) using a PrimeScript® RT reagent kit (Takara Bio, Inc.), according to the manufacturer's protocol. RT-qPCR was conducted using a Mir-XTM miRNA qPCR SYBR® kit (Takara Bio, Inc.) and SYBR Premix Ex Taq II (Takara Bio, Inc.) on an ABI 7300 plus system. U6 was used as the internal reference for miR-142-3p expression. GAPDH was used as internal reference for mRNA expression. The SIRT1 primer sequences were: 5′-TAGCCTTGTCAGATAAGGAAGGA-3′ and 5′-ACAGCTTCACAGTCAACTTTGT-3′. The GAPDH primer sequences were: 5′-CTGGGCTACACTGAGCACC-3′ and 5′-AAGTGGTCGTTGAGGGCAATG-3′. The primers for miR-142-3p (cat. no. HmiRQP0186) and U6 (cat. no. HmiRQP9001) were purchased from Guangzhou Fulengen Co., Ltd. (Guangzhou, China); sequences were not supplied. The PCR reaction conditions were: 95°C for 3 min, followed by 40 cycles of denaturation at 95°C for 15 sec and annealing/elongation at 60°C for 30 sec. The relative expression was analyzed using the 2−ΔΔCq method (23).

Drug sensitivity assay

The drug sensitivity of SKOV3/DDP cells was measured using a Cell Counting kit-8 (CCK)-8 assay. SKOV3/DDP cells (1×105 cells/ml) were seeded in 96-well plates and cultured at 37°C for 24 h. Cells were treated with cisplatin (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) at various concentrations (2, 4, 8, 16, 32, 64, 128, 256 and 512 µg/ml). Following incubation at 37°C for 48 h, 10 µl CCK-8 reagent (Sigma-Aldrich; Merck KGaA) was added into each well and then cells were cultured at 37°C for 2 h. The absorbance of each sample was measured at 450 nm using a plate reader (TECAN Infinite M200; Tecan Group, Ltd., Männedorf, Switzerland).

Western blot analysis

Tissues and all cells lines used in this study were lysed in cold radioimmunoprecipitation assay buffer (Beyotime Institute of Biotechnology, Haimen, China). Protein concentration was determined using a Bicinchoninic Acid Protein Assay kit (Pierce; Thermo Fisher Scientific, Inc.), according to the manufacturer's protocols. The protein (50 µg per lane) was separated via 12% SDS-PAGE (Pierce; Thermo Fisher Scientific, Inc.) and then transferred onto a polyvinylidene difluoride (PVDF) membrane (Thermo Fisher Scientific, Inc.). Following blocking in 5% non-fat dried milk in PBS at room temperature for 3 h, the PVDF membrane was incubated with rabbit anti-SIRT1 primary antibody (1:100; ab32441; Abcam, Cambridge, MA, USA) or rabbit anti-GAPDH primary antibody (1:100; cat. no. ab9485; Abcam) at room temperature for 3 h. Following washing with PBS with Tween-20 for 10 min, the membrane was incubated with the horseradish peroxidase conjugated goat anti-rabbit secondary antibody (1:5,000; cat. no. ab205718; Abcam) at room temperature for 1 h. Results were visualized using an enhanced chemiluminescence kit (Pierce; Thermo Fisher Scientific, Inc.). Protein expression levels were analyzed with Image-Pro Plus software 6.0 (Media Cybernetics, Inc., Rockville, MD, USA). GAPDH was used as the internal reference.

Cell proliferation analysis

SKOV3 cells (2×104) were seeded in 96-well plates, each well with 100 µl of fresh serum-free medium with 0.5 g/l MTT (Sigma-Aldrich; Merck KGaA). This cell line was selected as it demonstrated that the lowest expression of miR-142-3p. Following incubation at 37°C for 0, 24, 48 and 72 h, the medium was removed and 50 µl dimethyl sulfoxide (Sigma-Aldrich; Merck KGaA) was added. Following incubation at 37°C for 10 min, the absorbance of each sample was measured at 570 nm using a plate reader (TECAN Infinite M200; Tecan Group, Ltd.).

Bioinformatics analysis

TargetScan version 7.1 (www.targetscan.org) was used to predict the target genes of miR-142-3p, according to the manufacturer's protocol.

Dual luciferase reporter assay

The wild type (WT) or mutant type (MT) of SIRT1 3′UTR was inserted into the multiple cloning site of the psiCHECK™2 vector (Promega Corporation, Madison, WI, USA). SKOV3 cells were co-transfected with 100 ng WT-SIRT1-3′UTR or MT-SIRT1-3′UTR plasmid, and 100 nM miR-142-3p mimic or miR-NC using Lipofectamine® 2000, according to the manufacturer's protocols. Following transfection for 48 h, the Renilla luciferase activity and firefly luciferase activity were determined using a Dual-Luciferase Reporter Assay system (Promega Corporation), according to the manufacturer's protocol. Firefly luciferase activity was normalized to Renilla luciferase activity.

Statistical analysis

All data in the present study are expressed as the mean ± standard deviation. Statistical analysis was conducted using SPSS 19.0 (IBM Corp., Armonk, NY, USA). The difference between two groups was analyzed using Student's t-test and differences among >2 groups were analyzed using one-way analysis of variance, followed by a post hoc Turkey's post hot test. The association between miR-142-3p expression and clinicopathological characteristics of patients with ovarian cancer was analyzed using the Chi-square test. Pearson correlation analysis was conducted for the correlation between miR-142-3p and SIRT1 mRNA expression in ovarian cancer tissues. P<0.05 was considered to indicate a statistically significant difference. All analyses were performed in triplicate.

Results

Downregulation of miR-142-3p in ovarian cancer is associated with poor differentiation

Firstly, RT-qPCR data revealed that miR-142-3p expression levels were significantly reduced in ovarian cancer tissues compared with in adjacent tissues (Fig. 1A). To confirm these findings, the expression of miR-142-3p in several common ovarian cancer cell lines was investigated. As demonstrated in Fig. 1B, the expression levels of miR-142-3p were significantly lower in ovarian cancer cell lines compared with in the normal human ovarian epithelial cell line IOSE386 (Fig. 1B). Thus, miR-142-3p is downregulated in ovarian cancer. In addition, patients were categorized into a high miR-142-3p expression group and low miR-142-3p expression group, based on the mean expression value of miR-142-3p. Further investigation revealed that decreased expression levels of miR-142-3p were significantly associated with poor differentiation (Table I).

Figure 1. miR-142-3p expression in ovarian cancer. (A) miR-142-3p expression levels were reduced in ovarian cancer tissues compared with in adjacent non-tumor tissues. **P<0.01 vs. Adjacent tissues. (B) miR-142-3p expression levels were reduced in ovarian cancer cell lines compared with in the normal human ovarian epithelial cell line IOSE386. **P<0.01 vs. IOSE386 cells. miR, microRNA.

miR-142-3p suppresses the proliferation and chemoresistance of ovarian cancer cells

The effect of miR-142-3p on the proliferation of ovarian cancer cells was investigated. SKOV3 cells were transfected with miR-142-3p mimic to upregulate its expression. Transfection with miR-142-3p mimic revealed a significant increase in miR-142-3p expression levels in SKOV3 cells compared with in the control group. However, transfection with miR-NC did not affect the expression of miR-142-3p in SKOV3 cells (Fig. 2A). As the transfection with miR-NC did not affect miR-142-3p expression when compared with the control group, the proliferation of SKOV3 cells in the control group was not assessed. An MTT assay was then used to analyze cell proliferation, which demonstrated that the proliferation of SKOV3 cells was significantly reduced within the miR-142-3p-transfected group at 72 h compared with in cells transfected with miR-NC (Fig. 2B). Thus, miR-142-3p may serve a suppressive role in ovarian cancer cell proliferation.

Figure 2. Effect of miR-142-3p on ovarian cancer cell proliferation and chemoresistance. SKOV3 cells were transfected with miR-142-3p mimic or miR-NC, respectively, and non-transfected SKOV3 cells were used as the control group. Post-transfection, (A) RT-qPCR was used to determine miR-142-3p expression levels. **P<0.01 vs. Control. (B) An MTT assay was conducted to examine cell proliferation. **P<0.01 vs. miR-NC. Subsequently, SKOV3/DDP cells were transfected with miR-142-3p mimic or miR-NC, respectively, and non-transfected SKOV3/DDP cells were used as the control group. Post-transfection, (C) RT-qPCR was used to determine the miR-142-3p levels. **P<0.01 vs. Control. (D) An MTT assay was conducted to examine cell proliferation. **P<0.01 vs. miR-NC. miR, microRNA; NC, negative control (scrambled); RT-qPCR, reverse transcription-quantitative polymerase chain reaction; SKOV3/DDP, cisplatin-resistant SKOV3 cells.

The role of miR-142-3p in chemoresistance of ovarian cancer cells was investigated. Cisplatin-resistant SKOV3/DDP cells were transfected with miR-142-3p mimic or miR-NC, respectively. Following transfection, the miR-142-3p levels were significantly increased in the miR-142-3p group compared with in the control group; transfection with miR-NC demonstrated no effect on the expression of miR-142-3p in SKOV3/DDP cells (Fig. 2C). As the transfection with miR-NC did not affect miR-142-3p expression when compared with the control group, the survival rate of SKOV3/DDP cells in the control group was not assessed. A CCK-8 assay was conducted to assess the survival rate of cells treated with various concentrations of cisplatin. Under the same concentration of cisplatin (from 4, 8, 16, 32 and 64 µg/ml), the survival rate of SKOV3/DDP cells was significantly reduced in the miR-142-3p group compared with in the miR-NC group (Fig. 2D). These findings suggested that miR-142-3p may promote the sensitivity of SKOV3/DDP cells to cisplatin.

SIRT1 is a direct target gene of miR-142-3p in ovarian cancer cells

Based on the bioinformatics analysis data, SIRT1 was reported to be a putative target gene of miR-142-3p (Fig. 3A). To confirm this prediction, luciferase vectors containing WT or MT SIRT1 3′-UTR were employed (Fig. 3B). Luciferase reporter assay data indicated that luciferase activity was significantly reduced in SKOV3 and SKOV3/DDP cells co-transfected with the WT-SIRT1-3′UTR plasmid and miR-142-3p mimic, but unaltered in SKOV3 cells co-transfected with the MT-SIRT1-3′UTR plasmid and miR-142-3p mimic, when compared with the control group (Fig. 3C and D). Therefore, miR-142-3p may bind to the 3′UTR of SIRT1 mRNA in ovarian cancer SKOV3 and SKOV3/DDP cells.

Figure 3. Identification of target gene of miR-142-3p. (A) TargetScan software indicated that SIRT1 is a target gene of miR-142-3p. (B) Luciferase reporter vectors containing WT or MT of SIRT1 3′UTR were generated. (C and D) Luciferase activity was significantly reduced in SKOV3 and SKOV3/DDP cells co-transfected with the WT-SIRT1-3′UTR plasmid and miR-142-3p mimic, but were unaltered in SKOV3 and SKOV3/DDP cells co-transfected with the MT-SIRT1-3′UTR plasmid and miR-142-3p mimic, when compared with the control group. **P<0.01 vs. Control. miR, microRNA; SIRT1, sirtuin 1; MT, mutant type; SKOV3/DDP, cisplatin-resistant SKOV3 cells; 3′UTR, 3′-untranslated region; WT, wild-type.

In the present study, the effect of miR-142-3p on the expression of SIRT1 in ovarian cancer cells was analyzed. As presented in Fig. 4A and B, the mRNA and protein expression levels of SIRT1 in SKOV3 and SKOV3/DDP cells were significantly reduced in the miR-142-3p group compared with in the miR-NC group. To further confirm these data, SKOV3 and SKOV3/DDP cells were transfected with miR-142-3p inhibitor or NC inhibitor. Following transfection, miR-142-3p expression levels were significantly decreased in the miR-142-3p inhibitor group compared with in the control group; however, transfection with NC inhibitor did not markedly affect miR-142-3p expression in SKOV3 and SKOV3/DDP cells (Fig. 4C). Further investigation demonstrated that the mRNA and protein expression levels of SIRT1 were significantly higher in the anti-miR-142-3p group compared with in the anti-NC group (Fig. 4D and E). Collectively, these findings indicated that miR-142-3p may inhibit SIRT1 expression by directly binding to the 3′UTR of SIRT1 mRNA in ovarian cancer cells.

Figure 4. Effects of miR-142-3p on SIRT1 expression. (A) RT-qPCR and (B) western blotting were used to detect the mRNA and protein expression levels of SIRT1 in SKOV3 and SKOV3/DDP cells transfected with miR-142-3p mimic or miR-NC, respectively. **P<0.01 vs. miR-NC. Subsequently, SKOV3 and SKOV3/DDP cells were transfected with anti-miR-142-3p or anti-NC, respectively. Non-transfected cells were used as the control group. (C) Post-transfection, RT-qPCR was used to examine the miR-142-3p expression. **P<0.01 vs. Control. (D) RT-qPCR and (E) western blotting were used to detect the mRNA and protein expression levels of SIRT1. **P<0.01 vs. anti-NC. miR, microRNA; miR-NC, negative control (scramble) miR; anti-miR-142-3p, miR-142-3p inhibitor; anti-NC, negative control inhibitor; RT-qPCR, reverse transcription-quantitative polymerase chain reaction; SIRT1, sirtuin 1.

SIRT1 rescues the miR-142-3p-mediated suppression of proliferation and chemoresistance of ovarian cancer cells

Based on the aforementioned findings, it was suggested that SIRT1 may be involved in miR-142-3p-mediated suppression of ovarian cancer cell proliferation and chemoresistance. To clarify this speculation, miR-142-3p-overexpressing SKOV3 cells were transfected with an SIRT1-expression plasmid to upregulate its expression, or a blank vector as the control. Following transfection, the mRNA and protein levels of SIRT1 were significantly increased in the miR-142-3p + SIRT1 group compared with in the miR-142-3p + blank group (Fig. 5A and B). MTT assay data further revealed that the proliferation of SKOV3 cells were significantly increased in the miR-142-3p + SIRT1 group compared with in the miR-142-3p + blank group at 48 and 72 h (Fig. 5C), indicating that SIRT1 may have rescued the suppressive effect of miR-142-3p on SKOV3 cell proliferation. Subsequently, miR-142-3p-overexpressing SKOV3/DDP cells were also transfected with an SIRT1-expression plasmid, and the mRNA and protein levels of SIRT1 were significantly upregulated following transfection (Fig. 5D and E). A CCK-8 assay was then conducted to assess the survival rates of SKOV3/DDP cells treated with cisplatin at various concentrations. Under the same concentrations of cisplatin, the survival rate was significantly higher at 4, 8, 16, 32 and 64 µg/ml in the miR-142-3p + SIRT1 group compared with in the miR-142-3p + blank group (Fig. 5F). Thus, SIRT1 rescued the miR-142-3p-mediated suppression of chemoresistance of SKOV3/DDP cells.

Figure 5. Effect of SIRT1 upregulation on miR-142-3p-mediated suppression of proliferation and chemoresistance of ovarian cancer cells. miR-142-3p-overexpressing SKOV3 cells were transfected with SIRT1 expression plasmid or a blank vector. Post-transfection, (A) RT-qPCR and (B) western blotting were used to detect the mRNA and protein expression of SIRT1. (C) An MTT assay was used to examine cell proliferation. Subsequently, miR-142-3p-overexpressing SKOV3/DDP cells were transfected with a SIRT1 expression plasmid or a blank vector. Post-transfection, (D) RT-qPCR and (E) western blotting was used to detect the mRNA and protein expression levels of SIRT1, and (F) a Cell Counting kit-8 assay was used to examine drug sensitivity. **P<0.01 vs. miR1423p + blank. miR, microRNA; blank, blank vector; SIRT1, sirtuin 1; RT-qPCR, reverse transcription-quantitative polymerase chain reaction.

SIRT1 is highly upregulated in ovarian cancer

The expression of SIRT1 in ovarian cancer tissues and cell lines was detected. The results indicated that SIRT1 mRNA expression levels were significantly higher in ovarian cancer tissues compared with in adjacent tissues (Fig. 6A). Additionally, the mRNA and protein expression levels of SIRT1 were significantly upregulated in ovarian cancer cell lines compared with in normal ovarian epithelial cells (Fig. 6B and C). In addition, a negative correlation between SIRT1 and miR-142-3p expression in ovarian cancer tissues was observed (Fig. 6D). These findings suggested that downregulation of miR-142-3p may contribute to the upregulation of SIRT1 in ovarian cancer.

Figure 6. SIRT1 expression in ovarian cancer. (A) RT-qPCR was used to analyze the mRNA expression levels of SIRT1 in ovarian cancer tissues compared with in matched adjacent non-tumor tissues. **P<0.01 vs. Adjacent tissues. (B) RT-qPCR and (C) western blotting were employed to examine the mRNA and protein expression levels of SIRT1 in ovarian cancer cell lines compared with in the normal human ovarian epithelial cell line IOSE386. **P<0.01 vs. IOSE386 cells. (D) A negative correlation between SIRT1 mRNA and miR-142-3p expression levels in ovarian cancer tissues was observed. miR, microRNA; RT-qPCR, reverse transcription-quantitative polymerase chain reaction; SIRT1, sirtuin 1.

Discussion

The regulatory mechanism of miR-142-3p underlying ovarian cancer progression and chemoresistance is largely unclear. In the present study, miR-142-3p expression levels were significantly lower in ovarian cancer tissues and cell lines, when compared with those in adjacent tissues and normal human ovarian epithelial cell line IOSE386, respectively. The reduced expression of miR-142-3p was significantly associated with advanced malignancy. Ectopic expression of miR-142-3p significantly inhibited the proliferation of ovarian cancer cells and increased the sensitivity of SKOV3/DDP cells to cisplatin. SIRT1 was identified as a target gene of miR-142-3p and its expression was negatively regulated by miR-142-3p in ovarian cancer cells. Further investigation demonstrated that SIRT1 rescued the suppressive effects of miR-142-3p on the proliferation and chemoresistance of ovarian cancer cells. In addition, SIRT1 was significantly upregulated in ovarian cancer; a negative correlation between the expression levels of SIRT1 and miR-142-3p in ovarian cancer tissues was observed.

miR-142-3p has been reported to serve a suppressive role in numerous common malignances (24). For instance, miR-142-3p inhibits the invasion of breast cancer cells by targeting Wiskott-Aldrich syndrome like, integrin aV and additional cytoskeletal elements (24). Furthermore, miR-142-3p may function as a potential tumor suppressor by directly targeting high mobility group box 1 in non-small-cell lung carcinoma (25). Recently, Wu et al (26) reported that the levels of serum miR-142-3p were lower in high-pathological grade of ovarian cancer than in low grade of ovarian cancer. These findings suggested that aberrant expression of miR-142-3p may be involved in the progression of ovarian cancer; miR-142-3p may serve as a serum biomarker to distinguish ovarian cancer of various grades. However, the expression levels of miR-142-3p in ovarian cancer tissues have not been previously been studied. In the present study, it was reported that miR-142-3p was significantly downregulated in ovarian cancer tissues and cell lines, and the reduced expression of miR-142-3p was associated with poor differentiation in ovarian cancer, suggesting that its downregulation may contribute to the malignant progression of ovarian cancer. Further investigation revealed that restoration of miR-142-3p expression significantly inhibited the proliferation of SKOV3 cells.

During chemotherapy, ovarian cancer cells are prone to drug resistance, which is associated with cancer recurrence and mortality (2). Thus, investigation into the molecular mechanism underlying chemoresistance in ovarian cancer is urgently required for identifying novel and effective therapeutic targets. In the present study, the overexpression of miR-142-3p significantly inhibited the resistance of cisplatin-resistant SKOV3/DDP cells. Similarly, miR-142-3p was previously reported to improve the drug sensitivity of acute myelogenous leukemia and NSCLC (27,28).

Subsequently, bioinformatics analysis and a luciferase reporter assay were performed to study the potential targets of miR-142-3p in ovarian cancer cells. The data of the present study indicated that SIRT1 may be a direct target gene of miR-142-3p, and its expression was negatively mediated by miR-142-3p in SKOV3 and SKOV3/DDP cells. SIRT1 has been demonstrated to regulate various cellular functions including DNA repair, cell survival and metabolism via the deacetylation of target proteins such as histone and p53 (29). Recently, Asaka et al (29) reported that SIRT1 promoted the growth and cisplatin resistance of endometrial carcinoma cells. Previous studies have demonstrated that the expression levels of SIRT1 were increased in cisplatin-resistant ovarian cancer tissues compared with in cisplatin-sensitive ovarian cancer tissues; SIRT1 significantly enhanced the proliferation, chemoresistance and aggressiveness of ovarian cancer cells by upregulating numerous antioxidant pathways to inhibit oxidative stress (21,30). Therefore, the results of the present study suggested that the suppressive effects of miR-142-3p on the proliferation and chemoresistance of ovarian cancer cells may have occurred via the inhibition of SIRT1 expression.

SIRT1 was previously reported to be significantly upregulated in malignant ovarian epithelial tumors compared with in benign and borderline epithelial tumors (30). Similarly, SIRT1 expression levels were upregulated in ovarian cancer tissues and cell lines compared with normal ovarian tissues and cells in the present study; a negative correlation between SIRT1 and miR-142-3p expression levels in ovarian cancer tissues was also observed. This suggested that upregulation of SIRT1 may be due to the decreased expression of miR-142-3p.

In conclusion, miR-142-3p, which is significantly downregulated in ovarian cancer, may serve a suppressive role in the proliferation and chemoresistance of ovarian cancer cells, at least partially via the direct targeting of SIRT1. Therefore, the findings of the present study suggest that miR-142-3p may be a promising therapeutic candidate for the treatment of ovarian cancer.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Authors' contributions

JG performed statistical analysis, and wrote and submitted the manuscript. ZD designed the study and revised the manuscript. NW, XL, YX, YC and SL performed cellular and molecular experiments.

Ethics approval and consent to participate

This study was approved by the First Affiliated Hospital of Xinxiang Medical University (Weihui, China). Written informed consent was obtained from all patients.

Consent for publication

Written informed consent was obtained from all patients.

Competing interests

The authors declare that they have no competing interests.

References