肾透明细胞癌
小RNA
癌症研究
运行x1
细胞生长
体内
转移
染色质免疫沉淀
肿瘤进展
调节器
生物标志物
肾细胞癌
生物
化学
癌症
医学
转录因子
基因表达
内科学
基因
发起人
生物技术
生物化学
遗传学
作者
Jianxin Xue,Shenhao Zhu,Feng Qi,Kai Zhu,Pu Cao,Jie Yang,Zengjun Wang
标识
DOI:10.3389/fonc.2021.610992
摘要
Recent evidences indicated that miRNAs played core role in the progression of clear cell renal cell carcinoma (ccRCC). However, its molecular mechanism in ccRCC is still remained unclear. The study was designed to identify the role and regulatory mechanism of miR-582-5p in ccRCC. In this study, the low expression level of miR-582-5p were detected by qRT-PCR in ccRCC patient tumor samples and ccRCC cell lines, respectively. The expression level of miR-582-5p was associated with tumor stage and metastasis. In vivo and in vitro experiments found miR-582-5p inhibit tumor growth via suppressing COL5A1 expression. Additionally, RUNX1 was identified as the negative regulator of miR-582-5p through database prediction and chromatin immunoprecipitation. Finally, the negative relation of RUNX1 and miR-582-5p was verified through rescue experiment both in vitro and in vivo . In summary, miR-582-5p, which was regulated by RUNX1, inhibited tumor growth and invasion by targeting COL5A1, indicating that miR-582-5p may act as a biomarker and that the RUNX1/miR-582-5p/COL5A1 axis could be a potential therapeutic target for ccRCC.
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