miR‑20a‑5p inhibits endometrial cancer progression by targeting janus kinase 1
- Authors:
- Published online on: March 30, 2021 https://doi.org/10.3892/ol.2021.12688
- Article Number: 427
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Copyright: © He et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Endometrial cancer (EC) is the most common gynaecological cancer in developed countries, and the incidence of EC is increasing rapidly worldwide (1,2). Over 189,000 cases of endometrial cancer are diagnosed worldwide per year and ~45,000 mortality cases (3,4). EC is a multi-factorial disease of which pathogenesis has not been fully elucidated. Most cases of EC are diagnosed at an early-stage and have a good prognosis after surgery alone; however, the 5-year survival rate is only 17% for patients with distant metastatic disease (5,6). It is therefore crucial to understand the underlying mechanisms of EC metastasis in order to develop effective strategies for EC diagnosis and therapy.
MicroRNAs (miRs) are a class of short non-coding RNAs that regulate gene expression at the post-transcriptional level by binding to the 3′ untranslated region (3′UTR) of target mRNA (7). Abnormal expression of miRNAs has been found in various types of tumor and is frequently associated with numerous aspects of tumor progression, including proliferation, differentiation, invasion, migration, apoptosis and senescence (8). Emerging evidence has revealed that several miRNAs are dysregulated in EC (9–11) and can act as either potent oncogenes or tumor suppressor genes (12–14). For example, miR-23a and miR-135a have been demonstrated to inhibit EC development (12,14). Conversely, miR-29b can inhibit the proliferation and decrease the migratory and invasive abilities of EC cells (13). miR-20a-5p is a member of the miR-17-92 cluster, which plays a complex role in tumorigenesis (15). Dysregulation of miR-20a-5p has been observed in various cancers, including colorectal cancer, cervical cancer, ovarian cancer and hepatocellular carcinoma (16). Ramón et al (17) reported that miR-20a-5p is significantly downregulated in cancerous endometrium compared with control endometrium. Furthermore, a negative correlation between vascular endothelial growth factor A protein expression and miR-20a expression is observed in EC specimens (17). However, the function and underlying mechanism of miR-20a-5p in EC remain poorly understood.
Janus kinase 1 (Jak1) is a member of a class of protein-tyrosine kinases which are involved in autoimmune diseases and malignancies (18,19). Jak1 phosphorylates the proteins named signal transducers and activators of transcription in response to interferon (20) and serves a critical role in cancer progression.
The present study aimed to examine the expression of miR-20a-5p in human EC tissues and to determine the association between miR-20a-5p expression and the clinicopathological characteristics of patients with EC. The effects of miR-20a-5p on cell proliferation, invasive ability and adhesion were investigated. Whether miR-20a-5p could inhibit EC progression by targeting janus kinase 1 (Jak1) was also evaluated. The findings from this study might provide a better understanding of EC pathogenesis.
Materials and methods
Tissue collection
The present study was approved by the Ethics Committee of The First Affiliated Hospital of Hebei North University (Zhangjiakou, Hebei, China). All patients provided written informed consent in compliance with the code of ethics of the World Medical Association (Declaration of Helsinki). Human EC tissues and paracancerous tissues were collected from 47 patients with EC who underwent surgical resection. None of the patients had received chemotherapy or radiotherapy prior to surgery. The tissue samples were immediately frozen in liquid nitrogen.
Cell culture and transfection
The normal human endometrial stromal cell line hESC (cat. no. BNCC340262) and the EC cell lines Ishikawa, KLE, HHUA and RL95-2 were purchased from BeNa Culture Collection. All cells were cultured in Dulbecco's modified Eagle's medium/F12 (Invitrogen; Thermo Fisher Scientific, Inc.) supplemented with 10% FBS (Invitrogen; Thermo Fisher Scientific, Inc.). HEK293 cells were purchased from the American Type Culture Collection and cultured in RPMI Medium 1640 (Invitrogen; Thermo Fisher Scientific, Inc.) supplemented with 10% FBS. Cells were placed at 37°C in a humidified incubator containing 5% CO2. Ishikawa cells were transfected with 2 µM miR-negative control (NC), 2 µM miR-20a-5p-mimic, 2 µM miR-20a-5p-inhibitor, 4 µg pcDNA3.1 or 4 µg Jak1-pcDNA3.1 (Shanghai GenePharma Co., Ltd.) using Lipofectamine 2000 (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturers' instructions. After 48 h, cells were observed under a fluorescence microscope and the transfection efficiency was >80% (Fig. S1).
Reverse transcription-quantitative (RT-q) PCR
miRNAs were isolated from tissues or cultured cells using mirVanaTM miR isolation kit (Ambion; Thermo Fisher Scientific, Inc.). Total RNA was isolated using TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc.). cDNA was synthesized from 5 ng of total RNA using the First Strand cDNA Synthesis kit (Fermentas; Thermo Fisher Scientific, Inc.) according to the manufacturers' instructions. The sequences of primers were as follows: Jak1, forward 5′-AGCGATGTCCTTACCACACC-3′, reverse 5′-CCTCAACACACTCAGGAGCA-3′; GAPDH, forward 5′-TCAACGACCACTTTGTCAAGCTCA-3′, reverse 5′-GCTGGTGGTCCAGGGGTCTTACT-3′; miR-20a-5p, forward 5′-TAAAGTGCTTATAGTGCAGGTAG-3′, reverse 5′-TGGTGTCGTGGAGTCG-3′; and U6, forward 5′-CTCGCTTCGGCAGCACA-3′ and reverse 5′-AACGCTTCACGAATTTGCGT-3′. Amplification and detection were performed with a SYBR-Green PCR kit (Applied Biosystems; Thermo Fisher Scientific, Inc.) on the ABI PRISM 7700 Sequence Detection System (Applied Biosystems; Thermo Fisher Scientific, Inc.). The thermocycling conditions were as follows: 95°C for 4 min, followed by 40 cycles of 95°C for 30 sec, 59°C for 30 sec and 72°C for 1 min with a final extension at 72°C for 5 min. The relative expression levels were normalized to endogenous controls U6 and GAPDH and were expressed as 2−ΔΔCq (21).
Western blotting
Tissues and cells were collected and lysed using RIPA buffer (Beyotime Institute of Biotechnology) at 4°C. Protein concentration was determined using the BCA Protein Assay kit (Beyotime Institute of Biotechnology). Proteins (40 µg) were separated by 10% SDS-PAGE and transferred onto PVDF membranes (EMD Millipore). Subsequently, membranes were blocked with 5% skimmed milk at 4°C overnight. After washing in Tris-buffered saline-Tween-20 (0.05%) solution, membranes were incubated with mouse monoclonal primary antibodies against Jak1 (1:400; cat. no. sc376996; Santa Cruz Biotechnology, Inc.) and GAPDH (1:1,000; cat. no. sc365062; Santa Cruz Biotechnology, Inc.) at 4°C overnight. Membranes were then incubated with IgG-horseradish peroxidase-conjugated secondary antibody (1:5,000; cat. no. sc2005; Santa Cruz Biotechnology, Inc.) at 37°C for 1 h. Pierce SuperSignal West Pico Chemiluminescent Substrate (Pierce Biotechnology, Inc.) was used to detect the signal on the membrane. The data were analyzed via densitometry using ImageJ software (version 1.8.0; National Institutes of Health) and normalized to expression of the internal control GAPDH.
Dual luciferase reporter assay
Plasmid constructs carrying wild type or mutant Jak1 3′UTR in the psiCHECK vector were cotransfected with miR-20a-5p mimic or miR NC into HEK293 cells using Lipofectamine 2000. miR-20a-5p mimic and miR NC were synthesized by Shanghai GenePharma Co., Ltd. and the sequences were as follows: miR-20a-5p mimic, sense, 5′-UAAAGUGCUUAUAGUGCAGGUAG-3′; miR-20a-5p mimic, antisense, 5′-ACCUGCACUAUAAGCACUUUAUU-3′. miR NC, 5′-UUGUACUACACAAAAGUACUG-3′. After 48 h, the luciferase activity was measured using the Dual-Luciferase Reporter 1000 System (Promega Corporation). Renilla luciferase activity was normalized to firefly luciferase activity to control transfection efficiency.
MTT assay
Cell proliferation was determined using a MTT Assay Kit from Abcam according to the manufacturers' instructions. Briefly, cells at the density of 1×104/well were cultured in 96-well plates for 24, 48, 72 and 96 h and were incubated with 10 µl of MTT reagent for 3 h at 37°C. Subsequently, MTT solvent was added to dissolve purple formazan crystals and cells were further incubated at 37°C for 15 min. Absorbance was read at 570 nm using a microplate reader (Bio-Rad Laboratories, Inc.).
Cell invasion assay
Transwell inserts (Corning) were precoated with Matrigel (1:20; Corning) 37°C for 30 min before seeding the cells. At 48 h post-transfection, cells were collected with serum-free media and seeded into the upper chamber at a final concentration of 5×104 cells/ml whereas medium containing 10% FBS was added into the lower chamber. After incubation at 37°C for 8 h, the non-invasive cells in the upper chamber were removed gently using cotton swabs. The cells that have invaded the bottom of the membranes were fixed with ethanol, stained with hematoxylin. Cells were observed under an inverted light microscope (CKX31, Olympus Corporation; magnification, ×400). The number of invaded cells was quantified by counting five randomly chosen microscopic fields.
Fibronectin adhesion assay
At 48 h post-transfection, cells were seeded at the density of 5×104 cells per well into 96-well plates that were precoated with 1% human plasma fibronectin-purified protein (EMD Millipore). After incubation at 37°C for 2 h, cells were washed with PBS three times and fixed with 3.7% formaldehyde at room temperature for 40 min. Cells were stained with 0.1% crystal violet solution at room temperature for 30 min and the crystal violet was then solubilized in 10% acetic acid solution. The absorbance was determined at 570 nm using a microplate reader (Bio-Rad).
Statistical analysis
Statistical analysis was performed using SPSS 19.0 (IBM Corp.). The data were presented as the means ± standard deviation and analyzed by Student's t-test or ANOVA followed by Bonferroni's post hoc test. P<0.05 was considered to indicate a statistically significant difference.
Results
miR-20a-5p is downregulated in EC tissues and associated with the clinicopathological characteristics of patients with EC
Expression of miR-20a-5p in EC and paracancerous tissues was examined by RT-qPCR. As presented in Fig. 1, miR-20a-5p was significantly downregulated in EC tissues compared with paracancerous tissues (P<0.01). Furthermore, miR-20a-5p expression was found to be significantly associated with the depth of myometrial invasion, FIGO stage, histologic grade and lymph node metastasis in patients with EC (Table I).
 | Table I.The association between miR-20a-5p expression and clinicopathologic features of EC patients. |
miR-20a-5p inhibits cell viability and invasive ability, and stimulates cell adhesion
Expression of miR-20a-5p in endometrial stromal cell line hESC and EC derived cell lines Ishikawa, KLE, RL95-2 and HHUA was examined by RT-qPCR. As presented in Fig. 2A, miR-20a-5p expression was significantly decreased in EC derived cells compared with hESC cells (P<0.01). To investigate the effect of miR-20a-5p on cell proliferation, invasive ability and adhesion, Ishikawa cell line, which exhibited the lowest miR-20a-5p level, was chosen for subsequent gain-of-function and loss-of-function experiments. miR NC, miR-20a-5p mimic and miR-20a-5p inhibitor were transfected into Ishikawa cells. As demonstrated in Fig. 2B, miR-20a-5p expression was significantly increased in mimic group and decreased in inhibitor group compared with NC group (P<0.01). Furthermore, Ishikawa cells transfected with miR-20a-5p-mimic showed decreased proliferation (P<0.05) and invasion ability (P<0.05), and increased adhesion ability compared with NC group (P<0.05). Ishikawa cells transfected with miR-20a-5p-inhibitor showed the opposite results (Fig. 2C-E).
Jak1 is upregulated and associated with miR-20a-5p expression in EC tissues
Jak1 mRNA and protein expression in EC and paracancerous tissues was examined by RT-qPCR and western blotting, respectively. As presented in Fig. 3A, the mRNA and protein expression of Jak1 was significantly increased in EC tissues compared with paracancerous tissues (P<0.05). Furthermore, Jak1 mRNA expression was negatively correlated with miR-20a-5p expression in EC tissues (P<0.01; Fig. 3B).
miR-20a-5p directly targets Jak1
To verify whether miR-20a-5p could directly target Jak1, Jak1 3′UTR reporter assay was performed in HEK293 cells. As seen in Fig. 4A, the luciferase activity of wild type Jak1 3′UTR was significantly decreased in cells transfected with miR-20a-5p-mimic compared with cells transfected with miR-NC (P<0.01); however, no change was observed in the mutant Jak1 3′UTR. Furthermore, results from RT-qPCR and western blotting demonstrated that the mRNA and protein expression of Jak1 was significantly decreased in Ishikawa cells transfected with miR-20a-5p-mimic but increased in cells transfected with miR-20a-5p-inhibitor (P<0.01 for mRNA expression; P<0.05 for protein expression; Fig. 4B).
Jak1 overexpression reverses the effects of miR-20a-5p on cell proliferation, invasive ability and adhesion
Jak1-pcDNA3.1 and the empty vector pcDNA3.1 were transfected into Ishikawa cells. The results demonstrated that Jak1 mRNA and protein expression was significantly increased in the Jak1-pcDNA3.1 group compared with pcDNA3.1 group (P<0.01 for mRNA, P<0.05 for protein; Fig. S2). To further investigate whether Jak1 was involved in mediating the effects of miR-20a-5p on cell proliferation, invasive ability and adhesion, Jak1-pcDNA3.1 was transfected into Ishikawa cells in the presence of miR-20a-5p mimic. The results demonstrated that Jak1 protein expression was significantly increased in cells transfected with the miR-20a-5p mimic and Jak1-pcDNA3.1 compared with cells transfected with miR-20a-5p-mimic only (P<0.01); however, the increased expression of miR-20a-5p in miR-20a-5p-mimic-transfected cells was not affected by Jak1-pcDNA3.1 transfection (Fig. 5A and B). Furthermore, the inhibitory effect of miR-20a-5p-mimic on cell proliferation and invasive ability, and the promotive effect of miR-20a-5p-mimic on cell adhesion were reversed by transfection with Jak1-pcDNA3.1 (P<0.05; Fig. 5C-E).
Discussion
Alteration in miR-20a-5p expression patterns is associated with endometrial growth, differentiation and carcinogenesis of the endometrium (22–24). Previous studies reported that miR-20a-5p is significantly decreased in the plasma and serum of patients with endometriosis, and that it serves important roles in the pathogenesis of endometriosis (22,23). Conversely, miR-20a-5p expression was found to be upregulated in endometriotic stromal cells (24). In addition, in vitro application of hypoxia results in downregulation of miR-20a-5p in Ishikawa cells (25). In the present study, downregulation of miR-20a-5p was observed in EC tissues and cell lines compared with paracancerous tissues and endometrial stromal cells, respectively. Furthermore, miR-20a-5p expression was significantly associated with the depth of myometrial invasion, FIGO stage, histologic grade and lymph node metastasis in patients with EC. Patients with lower miR-20a-5p expression exhibited lower FIGO stage and histologic grade, as well as less myometrial invasion and lymph node metastasis.
miR-20a-5p serves various roles according to the type of cancer. Previous studies have demonstrated that miR-20a-5p can induce radioresistance in hepatocellular carcinoma and nasopharyngeal cancer cells (26,27). Zhao et al (28) reported that miR-20a-5p can inhibit cell proliferation, mobility and invasiveness, and facilitate apoptosis in breast cancer. However, contrasting report indicated that miR-20a-5p promotes invasion and metastasis, and induces epithelial-mesenchymal transition of colorectal cancer cells (29). In the present study, miR-20a-5p was demonstrated to inhibit cell proliferation and cell invasive ability, as well as to induce cell adhesion ability. These findings were in agreement with a previous study reporting the suppressor role of miR-20a-5p in EC cell lines (30).
Numerous target genes of miR-20a-5p have been identified in previous studies, including cyclin D1, E2F transcription factor 3, interleukin-8 and dual specificity phosphatase 2 (16,31). In the present study, miR-20a-5p expression and Jak1 expression levels were negatively correlated in EC tissues. Furthermore, Jak1 was demonstrated to be a direct target of miR-20a-5p following dual luciferase reporter assay. A previous study has reported that activated Jak1 might contribute to carcinogenesis in leukemias, lymphomas and myeloproliferative neoplasms (32). Sexl et al (33) reported that Jak1-deficient cells are more tumorigenic than wild-type cells. Jak1 can also act as either an oncogene or a tumor suppressor under certain conditions (34). The present study demonstrated that miR-20a-5p could decrease Jak1 expression in EC cells, and that Jak1 overexpression could reverse the effects of miR-20a-5p-mimic on EC cell proliferation, invasive ability and adhesion. These results supported the notion that Jak1 could contribute to EC progression (35,36) and suggested that miR-20a-5p may play a tumor suppressive role in EC partly by decreasing Jak1 expression.
In the present study, miR-20a-5p expression was detected in four EC derived cell lines, and the results demonstrated that all these EC cell lines had significantly decreased miR-20a-5p expression compared with normal human endometrial stromal cells. Since Ishikawa cell line showed the lowest miR-20a-5p expression, it was selected for subsequent experiments. The present study was however limited because the gain- and loss-of-function experiments were only performed in the Ishikawa cell line. Functional experiments performed in additional cell lines is therefore required.
In conclusion, to the best of our knowledge, the present study was the first to demonstrate that miR-20a-5p expression was significantly correlated with the depth of myometrial invasion, FIGO stage, histologic grade and lymph node metastasis in patients with EC. In addition, miR-20a-5p expression and Jak1 mRNA expression were negatively correlated in EC tissues. Jak1 was confirmed as a novel target of miR-20a-5p, and miR-20a-5p acted as a tumor suppressor in EC at least partly through decreasing Jak1 expression. This study provided new insights into the underlying mechanisms of EC progression, and the findings suggested that miR-20a-5p and Jak1 may serve as potential therapeutic targets in EC. Further investigation is required to confirm the effect of miR-20a-5p in animal models of EC and to determine additional target genes of miR-20a-5p.
Supplementary Material
Supporting Data
Acknowledgements
Not applicable.
Funding
This study was funded by Key Project of Science and Technology Plan of Hebei Health Committee (grant no. 20212598).
Availability of data and materials
The data sets generated and analyzed during the present study are available from the corresponding author on reasonable request.
Authors' contributions
QX and YH conceived and designed the experiments, analyzed the data and prepared the manuscript. HM and JW conducted the experiments. YK contributed to data collection and analysis. All authors read and approved the final version.
Ethics approval and consent to participate
This study was approved by the Ethics Committee of The First Affiliated Hospital of Hebei North University (Zhangjiakou, Hebei, China).
Patient consent for publication
All patients provided written informed consent in compliance with the code of ethics of the World Medical Association (Declaration of Helsinki).
Competing interests
The authors declare that they have no competing interests.
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