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首页> 外文期刊>European review for medical and pharmacological sciences. >MicroRNA-645 promotes cell metastasis and proliferation of renal clear cell carcinoma by targeting GK5
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MicroRNA-645 promotes cell metastasis and proliferation of renal clear cell carcinoma by targeting GK5

机译:MicroRNA-645通过靶向GK5促进肾透明细胞癌的细胞转移和增殖

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OBJECTIVE: To dissect the functioning mode of miR-645 on renal clear cell carcinoma cell metastasis and growth, and provide therapeutic targets for renal clear cell carcinoma. PATIENTS AND METHODS: Quantitative Real-time PCR (qRT-PCR) assay was employed to detect miR-645 expression level. Wound healing assay and transwell assay were performed to investigate metastasis capacity of renal clear cell carcinoma cells. Cell Counting Kit 8 (CCK8) assay was incorporated to assess cell proliferation capacity. Flow cytometry was used to identify cell apoptosis and cell cycle distribution. Protein levels were assessed by Western blotting assay. The target gene was predicted and verified by bioinformatics analysis and luciferase assay. RESULTS: MiR-645 was upregulated in renal clear cell carcinoma tissues when compared with para-carcinoma tissues (n=32). Downregulated miR-645 could attenuate cell migration and invasion capacities, as well as inhibited cell proliferation capacity, promoted cell apoptosis and cell cycle arrest at G0/G1 phase. GK5 was chosen as the target gene of miR-645 by bioinformatics analysis and luciferase reporter assay. Moreover, silence of GK5 could rescue tumor suppression role of downregulated miR-645 on renal clear cell carcinoma metastasis. CONCLUSIONS: Knockdown of miR-645 exerted tumor-suppressive effects on renal clear cell carcinoma metastasis and growth via targeting GK5 in vitro, which provided an innovative and candidate target for diagnose and treatment of renal clear cell carcinoma.
机译:目的:探讨miR-645在肾透明细胞癌细胞转移和生长中的作用方式,为肾透明细胞癌的治疗提供依据。病人与方法:采用实时荧光定量PCR(qRT-PCR)检测miR-645的表达水平。进行伤口愈合测定和transwell测定以研究肾透明细胞癌细胞的转移能力。合并了细胞计数试剂盒8(CCK8)分析以评估细胞增殖能力。流式细胞仪用于鉴定细胞凋亡和细胞周期分布。通过蛋白质印迹分析评估蛋白质水平。通过生物信息学分析和荧光素酶测定法对目标基因进行了预测和验证。结果:与癌旁组织相比,肾透明细胞癌组织中的MiR-645上调(n = 32)。下调的miR-645可能减弱细胞迁移和侵袭能力,并抑制细胞增殖能力,促进细胞凋亡和细胞周期阻滞在G0 / G1期。通过生物信息学分析和荧光素酶报告基因分析,选择GK5作为miR-645的靶基因。此外,GK5沉默可以挽救下调的miR-645对肾透明细胞癌转移的抑制作用。结论:敲低miR-645通过靶向GK5在体外对肾透明细胞癌的转移和生长产生了肿瘤抑制作用,为肾透明细胞癌的诊断和治疗提供了一个创新的候选靶点。

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