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miR-21-5p 通过下调 ARHGAP24 促进肾细胞癌的进展。

miR-21-5p serves as a promoter in renal cell carcinoma progression through ARHGAP24 downregulation.

机构信息

Department of Urology, Area 3, Tangshan Gongren Hospital, LubeiDistrict, No.27 Wenhua Road, Tangshan, Hebei, 063000, People's Republic of China.

出版信息

Environ Sci Pollut Res Int. 2022 Jun;29(26):39985-39993. doi: 10.1007/s11356-021-18343-z. Epub 2022 Feb 3.

DOI:10.1007/s11356-021-18343-z
PMID:35112252
Abstract

Renal cell carcinoma (RCC) is a highly recurrent aggressive tumor. This study works for the regulation of miR-21-5p on RCC cell functions and novel ideas for therapies of RCC. Isoform expression quantification data were offered by The Cancer Genome Atlas Kidney Renal Clear Cell Carcinoma (TCGA-KIRC) to investigate differentially expressed miRNAs. The way miR-21-5p works on biological functions of RCC was examined with MTT and Transwell assays. The downstream targets of miR-21-5p were predicted using bioinformatics analysis. The binding of two researched objects was verified by the dual-luciferase method. TCGA data manifested a considerably high level of miR-21-5p in RCC tissue, while ARHGAP24 was significantly lowly expressed. miR-21-5p bound ARHGAP24 and stimulated RCC cell functions, whereas ARHGAP24 mimic could reverse such promotion. This work observed miR-21-5p, a stimulator in RCC, and it deteriorated this cancer via repressing its downstream target gene ARHGAP24 expression.

摘要

肾细胞癌(RCC)是一种高度复发的侵袭性肿瘤。本研究旨在探讨 miR-21-5p 对 RCC 细胞功能的调节作用,为 RCC 的治疗提供新的思路。本研究利用癌症基因组图谱肾透明细胞癌(TCGA-KIRC)提供的异构体表达定量数据,探讨差异表达的 miRNAs。通过 MTT 和 Transwell 检测分析 miR-21-5p 对 RCC 细胞生物学功能的影响。利用生物信息学分析预测 miR-21-5p 的下游靶基因。采用双荧光素酶报告基因实验验证两个研究对象的结合。TCGA 数据显示 RCC 组织中 miR-21-5p 水平显著升高,而 ARHGAP24 表达明显降低。miR-21-5p 与 ARHGAP24 结合并刺激 RCC 细胞功能,而 ARHGAP24 模拟物可以逆转这种促进作用。本研究观察到 miR-21-5p 作为 RCC 的一种刺激物,通过抑制其下游靶基因 ARHGAP24 的表达,恶化了这种癌症。

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