Tumor suppressor microRNA-136-5p regulates the cellular function of renal cell carcinoma

Abstract

MicroRNAs (miRs) are involved in diverse physiological and developmental processes at the post-transcriptional level in cells. Previous studies have demonstrated that miR-136-5p is involved in certain types of cancer. However, the function of miR-136-5p in renal cell carcinoma (RCC) remains to be fully elucidated. In present study, miR-136-5p expression levels were determined by reverse transcription-quantitative polymerase chain reaction (RT-qPCR), and MTT assays, CCK-8 assays, Transwell assays, wound healing assays and flow cytometry were performed to investigate the function of miR-136-5p in RCC. RT-qPCR revealed that the expression of miR-136 was significantly lower in RCC tissues and cells compared with adjacent non-tumor tissues and cells in vitro. miR-136-5pwas also demonstrated to be associated with RCC cell proliferation, viability, migration, invasion and apoptosis. miR-136-5p may therefore function as a tumor suppressor in RCC. Further studies are required to elucidate the molecular mechanisms and signaling pathways underlying these functions of miR-136-5p, to investigate the potential function of miR-136-5p as a biomarker for the early detection and prognosis of RCC, and its potential as a therapeutic target for the treatment of RCC.

Introduction

Renal cell carcinoma (RCC) is the third most common urological neoplasm following prostate and bladder cancer, and accounts for 2% of all cancer-associated mortality in the United States of America (1). The disease is comprised of >10 histological and molecular subtypes, of which clear cell RCC (ccRCC) is the most common, accounting for ~70% of all diagnosed cases (1,2). Prognosis is closely associated with the stage of RCC at the point of diagnosis. The 5-year survival rate of stage I RCC is ~95%, while that of stage IV is just 20% (2). Therefore, early detection of RCC is of great importance for successful treatment. However, during early stage RCC there are typically no clear symptoms, making diagnosis difficult, and ~25–30% of patients with RCC are metastatic at diagnosis (3). At present, no standardized approaches to biomarker sampling or analysis have been adopted for RCC since the majority of the putative tumor markers themselves remain under active investigation for further validation (4). Reliable biomarkers have not yet been established for screening (2). In addition, there are no data suggesting that adjuvant therapies such as cytokines and vaccines were effective following RCC surgery (5).

MicroRNAs (miRNAs/miRs) are short, non-coding single stranded RNAs with 20–22 nucleotides that regulate the expression of their target genes at the post-transcriptional level (6). An increasing body of evidence implicates miRNAs in various aspects of tumorigenesis (1). In addition, certain miRNAs are considered to be potential cancer biomarkers and anti-cancer therapeutics (7). Previous studies have demonstrated that several miRNAs are dysregulated in RCC, and result in aberrant cell growth, angiogenesis, apoptosis and autophagy (6,8–10).

Previous studies have demonstrated that miR-136-5p is involved in a number of types of carcinoma, including glioma (11), triple-negative breast cancer (12) and non-small cell lung cancer (NSCLC) (13). However, the function of miR-136-5p in RCC remains to be explored. In the present study, miR-136-5p was revealed to function as a tumor suppressor in RCC, as it repressed migration, invasion, viability, proliferation and promoted apoptosis in in vitro experiments.

Materials and methods

Sample collection

A total of 28 tumor samples and matched non-tumor kidney tissues were obtained from Peking University Shenzhen Hospital (Shenzhen, China) between January 2015 and January 2016. The normal kidney tissue was obtained by sampling 2 cm away from the tumor tissue. The specimens were frozen in liquid nitrogen (−195.8°C) until RNA extraction. The present study was approved by the local Ethics Committee of Peking University Shenzhen Hospital (Shenzhen, China), and written informed consent was obtained from all patients. The clinic pathological features of all patients are listed in Table I.

Table I.

Clinicopathological features of patients with renal cell carcinoma.

Characteristic	No. of patients
Mean age, range (years)	45 (25–62)
Sex
Male	9
Female	19
Histological type
Clear cell	24
Papillary	4
pT-stage
T1	19
T2	7
T3+4	2
Fuhrmann grade
I	7
II	18
III	2
IV	1
AJCC clinical stage
I	8
II	18
III + IV	2

pT, primary tumor; AJCC, American Joint Committee on Cancer.

RNA extraction and reverse-transcription quantitative polymerase chain reaction (RT-qPCR)

Total RNA was extracted from the RCC tissue and adjacent tissue using TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA) and was purified using the RNeasy Maxi kit (Qiagen GmbH, Hilden, Germany) following the manufacturer's protocols. The concentration of the RNA was measured using a NanoDrop 2000/2000c spectrophotometer (NanoDrop Technologies; Thermo Fisher Scientific, Inc., Pittsburgh, PA, USA). The miScript Reverse Transcription kit (Qiagen GmbH) was used to prepare cDNA from 1 µg RNA. The reverse transcription process consisted of 37°C for 60 min, 95°C for 5 min and then storage at 4°C. To analyze the expression of miR-136-5p, qPCR was conducted using the resultant cDNA with the miScript SYBR^® Green PCR kit (Qiagen GmbH) following the manufacturer's protocol, on the Roche Light Cycler 480 Real-Time PCR System (Roche Diagnostics, Basel, Switzerland). The thermocycler conditions were as follows: 95°C for 1 min, 40 cycles of 95°C for 15 sec, 55°C for 30 sec and 72°C for 30 sec. The sequences of the primers for miR-136-5p and the internal control, U6, are presented in Table II. The 2^−ΔΔCq method was used to analyze the expression of miR-136-5p (14).

Table II.

Sequences of primers and miRs.

Primer	Sequence (5′-3′)
miR-136-5p
Forward	ACTCCATTTGTTTTGATGATGGA
Reverse	Reverse provided by the miScript SYBR® Green kit
U6
Forward	CTCGCTTCGGCAGCACA
Reverse	ACGCTTCACGAATTTGCGT
miR-136-5p mimics
Forward	ACUCCAUUUGUUUUGAUGAUGGA
Reverse	CAUCAUCAAAACAAAUGGAGUUU
NC
Forward	UUCUCCGAACGUGUCACGUTT
Reverse	ACGUGACACGUUCGGAGAATT
miR-136-5p inhibitor	UCCAUCAUCAAAACAAAUGGAGU
NC inhibitor	CAGUACUUUUGUGUAGUACAA

Cell culture and transfection

A normal human embryo kidney cell line (293T) and two RCC cell lines (786-O and ACHN) were obtained from the Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics (Shenzhen, China). Cells were cultured in Dulbecco's modified Eagle's medium (DMEM; Gibco; Thermo Fisher Scientific, Inc.) supplemented with 10% fetal bovine serum (FBS; Gibco; Thermo Fisher Scientific, Inc.), 1% penicillin-streptomycin (Gibco; Thermo Fisher Scientific, Inc.) and 1% glutamine (Gibco; Thermo Fisher Scientific, Inc.) at 37°C in a 5% CO₂ humidified incubator. Transfection was performed with miR-136-5p mimics, miR-136-5p inhibitors, negative control (NC) miRNA and inhibitor negative control (inhibitor NC) miRNA (5 pmol; Shanghai GenePharma Co., Ltd., Shanghai, China) using Lipofectamine 2000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol when cells were at 70% confluence. The sequences of mimics, inhibitor, NC and inhibitor NC are presented in Table II. Following transfection, RT-qPCR was used to assess transfection efficiency and the expression of miR-136-5p.

Cell Counting Kit-8 (CCK-8) assay

Cells (5×10³) transfected with 5 pmol miR-136-5p mimics, inhibitors, NC or inhibitor NC were seeded in 96-well plates and then incubated at 37°C. After 0, 24, 48 and 72 h, 10 µl CCK-8 reagent (Beyotime Institute of Biotechnology, Haimen, China) was added into each well of a 96-well plate for 30 min at 37°C, and then the absorbance values of the experimental wells were read at 490 nm.

MTT assay

Following transfection with 5 pmol miR-136-5p mimics, NC, miR-136-5p inhibitors or inhibitor NC, ~5×10³ cells were seeded into each well of a 96-well plate and incubated for 4 days. Following addition of 20 µl MTT (5 mg/ml; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) to the plate, the cells were incubated for a further 4 h at 37°C. The medium was discarded, 100 µl DMSO was added into each well, and the plates were shaken on a reciprocating decolorization shaking table (TSB-108 Qilinbeier, Jiangsu, China; http://www.qilinbeier.cn/tsb-108.html) for 10 min in the dark. Then, the absorbance values were read at 595 nm using an ELISA microplate reader (680; Bio-Rad Laboratories, Inc., Hercules, CA, USA).

Wound healing assay

Cells (5×10⁵) were seeded into each well of a 12-well plate, and incubated until they formed a monolayer of ~80% confluent cells. Cells were then transfected with 100 pmol chemically synthesized miRNA-136-5p inhibitors, mimics, NC or inhibitor NC, as aforementioned. A wound was created with a sterile 200 µl pipette tip, and floating cells were washed away using phosphate-buffered saline (PBS). Cell images were taken at 0 and 12 h after making the scratch using a digital camera system, and the temperature of incubation subsequent to making the scratch was 37°C.

Transwell assay

Transwell chamber inserts (BD Biosciences, Franklin Lakes, NJ, USA) with or without Matrigel (for invasion assays) were used. Serum-free medium (200 µl DMEM) containing ~1×10⁴ transfected cells was seeded into upper chamber of the insert. Medium mixed with 10% FBS was added to the lower chamber of the inserts. 786-O cells and ACHN cells were incubated at 37°C for 36 h for the migration assay, and were incubated for 48 and 60 h, respectively, for the invasion assay. All non-migrated cells were removed by a cotton swab. The cells that had migrated or invaded to the other side of the membrane were stained with 0.1% crystal violet for 25 min at 25°C and counted for in three fields of view using a microscope (Leica DMIRB Inverted Fluorescence Microscope, Leica Microsystems GmbH, Wetzlar, Germany).

Flow cytometry assay

Cells were seeded in a 6-well plate (3×10⁵ cells/well) and maintained in a humidified incubator with 5% CO² at 37°C until they formed an ~80% confluent monolayer. Cells were then transfected with 200 pmol miR-136-5p mimics, inhibitors, NC or inhibitor NC. Following transfection for 48 h, cells were gathered and washed twice with cold PBS. Then, the cells were re-suspended in 100 µl 1X binding buffer (Alexa Fluor 488 Annexin V/Dead Cell Apoptosis kit, Invitrogen; Thermo Fisher Scientific, Inc.) to create a single-cell suspension. Cell suspension (50 µl), 5 µl Annexin V-fluorescein isothiocyanate and 5 µl propidium iodide (Alexa Fluor 488 Annexin V/Dead Cell Apoptosis kit) were mixed and then incubated in room temperature for 15 min in the dark Following the addition of 400 µl binding buffer, the samples were analyzed using a flow cytometer (EPICS, Xl-4; Beckman Coulter, Inc., Brea, CA, USA), and the software used for data analysis was FlowJo v 10 (TreeStar, Inc., Ashland, OR, USA).

Bioinformatics analysis

Potential targets of miR-136-5p were predicted through the combination of four public algorithms, including miRWalk (15) (www.umm.uni-heidelberg.de/apps/zmf/mirwalk), miRanda (16) (www.microrna.org), PicTar (pictar.mdc-berlin.de) and TargetScan (17) (www.targetscan.org). All four algorithms accepted the predicted genes, which were selected based on gene function.

Statistical analysis

Each experiment was performed in triplicate and repeated at least three times. The data are presented as the mean ± standard deviation. MiR-136 expression levels between groups were analyzed using paired Student's t-tests, with the exception of relative expression of miR-136-5p in cells as presented in Fig. 1, which was analyzed using one-way analysis of variance followed by Dunnett's post hoc test. A paired Student's t-test was also used to analyze the results of assays to characterize cell phenotype. All statistical calculations were performed using SPSS 19.0 software (IBM Corp., Armonk, NY, USA). P<0.05 was considered to indicate a statistically significant difference.

Figure 1.

(A) Log₂ ratios (T/N) of miR-136-5p in 28 paired renal cell carcinoma tissues. (B) Relative expression levels of miR-136-5p in RCC and normal tissues. (C) Relative expression levels of miR-136-5p in 293T, ACHN and 786-O cell lines. (D) Relative expression levels of miR-136-5p in RCC cell lines following transfection. *P<0.05, **P<0.01 and ***P<0.001, vs. the respective controls. miR, microRNA; NC, negative control; T, renal cell carcinoma tissues; N, normal tissues.

Results

miR-136-5p is downregulated in RCC tissues and cell lines

RT-qPCR was performed to examine the expression levels of miR-136-5p in 28 paired RCC tissues and cell lines. As presented in Fig. 1A, the ratio of miR-136-5p expression [log₂Ratio (T/N)] was revealed to be downregulated in the RCC tissues from 22/28 patients. Mean expression levels are presented in Fig. 1B, and revealed that the expression of miR-136-5p in RCC tissues was significantly decreased compared with adjacent normal tissues (P<0.01). Furthermore, miR-136-5p expression levels were significantly decreased in ACHN (P<0.05) and 786-O (P<0.05) RCC cell lines compared with the 293T normal kidney human embryo kidney cell line, as presented in Fig. 1C.

Validation of cell transfection efficiency

qPCR was performed to assess the transfection efficiency of miR-136-5p mimics or NC and miR-136-5p inhibitors or inhibitor NC. Compared with the NC group, the expression levels of miR-136-5p were 145.00 times higher in ACHN cells (P<0.01) and 67.33 times higher in 786-O cells (P<0.001) transfected with miR-136-5p. Compared with the inhibitor NC group, miR-136-5p expression levels were 0.16 times that in ACHN cells (P<0.01) and 0.09 times that in 786-O cells (P<0.001) following transfection with miR-136-5p inhibitors (Fig. 1D).

Upregulation of miR-136-5p inhibits RCC cell proliferation and downregulation of miR-136-5p promotes RCC cell proliferation

The effect of miR-136-5pon proliferation was determined using a CCK-8 assay (Fig. 2). Following transfection with miR-136-5p mimics, the proliferation of ACHN cells was decreased by 13.97% (24 h; P<0.01), 28.15% (48 h; P<0.01) and 19.21% (72 h; P<0.01), while that of 786-O cells was decreased by 6.67% (24 h), 14.35% (48 h; P<0.05) and 17.62% (72 h; P<0.001), respectively, compared with the NC group (Fig. 2A and C). Furthermore, following transfection with miR-136-5p inhibitors, the proliferation of ACHN cells was increased by 10.15% (24 h; P<0.05), 28.30% (48 h; P<0.01) and 40.19% (72 h; P<0.01), while that of 786-O cells was increased by 8.29% (24 h; P<0.05), 11.97% (48 h; P<0.05) and 20.45% (72 h; P<0.001), respectively, compared with the inhibitor NC group (Fig. 2B and D).

Figure 2.

Analysis of cell proliferation and viability with CCK-8 and MTT assays. ACHN cells were transfected with (A) miR-136-5p mimics and NC and (B) miR-136-5p inhibitors and inhibitor NC, and proliferation was assessed using a CCK-8 assay. 786-O cells were transfected with (C) miR-136-5p mimics and NC and (D) miR-136-5p inhibitors and inhibitor NC, and proliferation was assessed using a CCK-8 assay. Cell viability was analyzed in (E) ACHN and (F) 786-O cells using an MTT assay. *P<0.05, **P<0.01 and ***P<0.001 vs. the respective controls. CCK-8, Cell Counting Kit 8; miR, microRNA; NC, negative control; OD, optical density.

Upregulation of miR-136-5p inhibits RCC cell viability and downregulation of miR-136 promotes RCC cell viability

The effect of miR-136-5p on cell viability was determined using an MTT assay. As presented in Fig. 2E, the viability of ACHN cells transfected with the miR-136-5p mimic was reduced by 12.89% (P<0.01) compared with the NC group, while the viability of cells transfected with the miR-136-5p inhibitor was increased by 16.39% (P<0.01) compared with the inhibitor NC group. Similarly, the viability of 786-O cells transfected with the miR-136-5p mimic was decreased by 16.71% (P<0.05) compared with the NC group, while the viability of cells transfected with the miR-136-5p inhibitor was increased by 13.15% (P<0.05) compared with the inhibitor NC group (Fig. 2F).

Upregulation of miR-136-5p inhibits RCC cell migration and invasion, while downregulation of miR-136-5p promotes RCC cell migration and invasion

The effect of miR-136-5p on RCC cell mobility was determined using wound healing assays and Transwell assays (Figs. 3 and 4). Representative images of the wound healing assay are presented in Fig. 3A. The wound healing assay revealed that, compared with the NC group, the migration of the mimic group was reduced by 28.53% (P<0.05; Fig. 3C) in ACHN cells and by 27.99% (P<0.05; Fig. 3B) in 786-O cells 12 h following the initial scratch. In contrast, compared with the inhibitor NC group, the migration of the inhibitor group was increased by 73.14% (P<0.01; Fig. 3C) in ACHN cells and by 31.08% (P<0.05; Fig. 3B) in 786-O cells 12 h following the initial scratch.

Figure 3.

Analysis of migration using wound healing assays. (A) Representative migratory images (magnification, ×100). Migratory distances in (B) 786-O cells and (C) ACHN cells following transfection. *P<0.05 and **P<0.01, with comparisons indicated by lines. miR, microRNA; NC, negative control.

Figure 4.

Migration and invasion were assessed using Transwell assays. (A) Representative images (magnification, ×100) of migrating and invading 786-O and ACHN cells, with quantification in (B) 786-O cells and (C) ACHN cells. *P<0.05 and **P<0.01, with comparisons indicated by lines. miR, microRNA; NC, negative control.

As presented in Fig. 4C, the Transwell assay revealed that, following transfection with miR-136-5p mimics, ACHN cell migration was reduced by 60.34% compared with the NC group (P<0.01), while the cells transfected with miR-136-5p inhibitors was increased by 100.26% compared with the inhibitor NC group (P<0.01). The invasion of ACHN cells transfected with miR-136-5p mimics was reduced by 75.52% compared with the NC group (P<0.01), while the invasion of cells transfected with miR-136-5p inhibitors was increased by 109.52% compared with the inhibitor NC group (P<0.05; Fig. 4C). Similarly, the migration of 786-O cells transfected with miR-136-5p mimics was reduced by 49.02% compared with the NC group (P<0.01), while the migration of cells transfected with miR-136-5p inhibitor was increased by 84.09% compared with the inhibitor NC group (P<0.05; Fig. 4B). The invasion of 786-O cells transfected with miR-136-5p mimics was reduced by 78.41% compared with the NC group (P<0.01), while the cells transfected with miR-136-5p inhibitors was promoted by 60.63% compared with the inhibitor NC group (P<0.01; Fig. 4B).

Upregulation of miR-136-5p induces apoptosis and downregulation of miR-136-5p suppresses cell apoptosis

Flow cytometry was used to assess the effect of miR-136-5p on apoptosis (Fig. 5A). The results revealed that the early apoptosis rate of 786-O cells transfected with miR-136-5p mimics and NC was 27.56±0.40 and 16.73±0.26%, respectively (P<0.01; Fig. 5B), while the early apoptosis rate of 786-O cells transfected with miR-136-5p inhibitors and inhibitor NC was 12.93±0.34 and 17.66±0.32%, respectively (P<0.05; Fig. 5B). Similarly, the early apoptosis rate of ACHN cells transfected with miR-136-5p mimics and NC was 31.4±0.78 and 24.26±0.66%, respectively (P<0.05; Fig. 5C), while the early apoptosis rate of ACHN cells transfected with miR-136-5p inhibitors and inhibitor NC was 15.03±0.93 and 24.33±0.72%, respectively (P<0.05; Fig. 5C).

Figure 5.

Apoptosis was analyzed with flow cytometry. (A) Representative flow cytometry results in 786-O and ACHN cells, with quantification in (B) 786-O cells and (C) ACHN cells. *P<0.05 and **P<0.01, with comparisons indicated by lines. miR, microRNA; PI, propidium iodide; FITC, fluorescein isothiocyanate; NC, negative control.

Target gene prediction

Four algorithms were combined to predict the putative target genes of miR-136-5p. All four algorithms simultaneously predicted that dedicator of cytokinesis 5 (DOCK5) was a potential target. The complementary site for the seed sequences of miR-136-5p was 5′-AAUGGAGA-3′ in the DOCK5 3′-untranslated region.

Discussion

MiRNAs may be critical in the development, proliferation, communication and death of cells, as well as in tissue differentiation (18). Emerging evidence suggests that miRNAs are involved in tumor development and progression (19). In the present study, miR-136-5p was revealed to be downregulated in RCC tissues and cell lines compared with adjacent non-tumor tissues and cells in vitro. Furthermore, cell proliferation, migration and invasion were demonstrated to be suppressed following upregulation of miR-136-5p. Apoptosis was also induced by upregulation of miR-136-5p.

Previous studies have provided evidence that miR-136-5p serves either an oncogenic or a tumor-suppressing function in the development of carcinomas. For example, in NSCLC, expression of miR-136-5p promoted cell proliferation by promoting extracellular signal-regulated kinase (ERK)1/2 phosphorylation via the targeting of protein phosphatase 2 regulatory subunit Bα (PPP2R2A) (13). This result supports the hypothesis that miR-136 acts as an oncogene in NSCLC.

In contrast, Jeong et al (11) demonstrated that miR-136-5p targeted the Notch3 oncogene and functions as an ovarian cancer suppressor (11). miR-136-5p was also reported to be downregulated in triple-negative breast cancer by targeting RAS protein activator like 2, and act as a tumor suppressor (12). Yang et al (20) also described miR-136-5p as a tumor suppressor in lung adenocarcinoma, and revealed that this occurred through the targeting of SMAD family member (Smad)2 and Smad3. In a previous study, miR-136-5p was revealed to be downregulated in metastatic giant cell bone tumors compared to non-metastatic giant cell bone tumors, by promoting nuclear factor I B expression (21). In another study concerning glioma, miR-136-5p was revealed to serve a tumor-suppressive function in human glioma by upregulating the expression of astrocyte elevated gene-1 and B cell lymphoma-2 (BCL2) (22). In another study, overexpression of miR-136-5p negatively impacted proliferation of the LN229 glioblastoma cell line by downregulating matricellular cysteine rich angiogenic inducer 61 protein expression (23). miR-136-5p was also reported to be serve as an anti-oncogene in epithelial ovarian cancer (24). Gao et al (25) demonstrated that colorectal neoplasia differentially expressed is a target of miR-136-5p in colorectal cancer cells, and high levels of miR-136-5p may inhibit the migration and invasion of colorectal cancer cells. Consistent with these results, the present study demonstrated that transfection with miR-136-5p mimics inhibited proliferation, invasion, and migration and induced apoptosis in the 780-O and ACHN cell lines, supporting the hypothesis that miR-136-5p is a tumor-suppressor in RCC. Together, these data indicate that the biological function of miR-136 is involved in the tumorigenesis and progression of various types of human cancer.

In addition, miRNAs may be used as biomarkers to improve our knowledge on diagnosis, prognosis and drug resistance, and may be used as therapeutic approaches in certain types of cancer. For example, miR-136-5p may be a potential biomarker for ccRCC (26). Overexpression of miR-136-5p may be associated with poor prognosis in giant cell bone tumors (18). Wu et al (27) reported that miR-136-5p functions as a predictor of the response to temozolomide therapy, and serves as a novel potential maker for glioma therapy. Chen et al (28) demonstrated that miR-136-5p was associated with cisplatin resistance and functions as a tumor suppressor in glioma. miR-136-5p has also been reported to inhibit cancer stem cell activity and increase the anti-tumor effect of paclitaxel on ovarian cancer chemotherapy tolerance (11). Zhao et al (29) reported that miR-136-5p may have therapeutic potential in hepatitis B virus-associated hepatocellular carcinoma. Therefore, miR-136-5p has the potential to be a diagnostic or a prognostic biomarker for RCC, and this should be confirmed by further research.

In addition to being associated with tumors, miR-136-5p is also associated with multiple non-neoplastic diseases. Ji et al (30) demonstrated that high level of miR-136-5p suppressed cell proliferation and promoted apoptosis of mesenchymal stem cells through targeting BCL2, which is a potential causal factor of preeclampsia. Zhang et al (31) demonstrated that miR-136-5p is involved in keratinocyte growth through targeting PPP2R2A, and may be a novel treatment target for the improvement of skin wound healing (31). Aberrant miR-136-5p upregulation in atherosclerosis contributes to abnormal vascular smooth muscle cell proliferation via the ERK1/2 signaling pathway by targeting PPP2R2A (32).

The mechanism underlying the effect of miR-136-5p in RCC requires further exploration, and improved understanding of the cellular function of ectopic miRNAs provides novel insights into RCC (33). In the present study, miR-136-5p was demonstrated to functions as a tumor suppressor in RCC, and may consequently serve as a therapeutic target for RCC.

In conclusion, the present study demonstrated that miR-136-5p served as a tumor suppressor, inhibited growth, viability, migration, invasion and induced apoptosis of RCC cells. Therefore, it may be associated with the development and progression of RCC. In addition, these results underscore the clinical potential of miR-136-5p in RCC treatment, and support the development of effective therapeutic strategies that target miR-136-5p.

Competing interests

The authors declare that they have no competing interests.