癌基因
小RNA
基因沉默
癌症研究
前列腺癌
抑制器
MTT法
生物
癌症
细胞生长
细胞培养
细胞
免疫印迹
荧光素酶
分子生物学
细胞周期
转染
基因
遗传学
作者
Hu Cy,You P,J Zhang,H Zhang,Ning Jiang
出处
期刊:PubMed
日期:2019-06-01
卷期号:23 (12): 5133-5138
被引量:19
标识
DOI:10.26355/eurrev_201906_18177
摘要
Researches have indicated that microRNA-506-3p (miR-506-3p) was downregulated and functioned as tumor suppressor in cancers. However, the biological role of miR-506-3p in prostate cancer (PCa) remains to be elucidated.Expression of miR-506-3p in PCa cell lines was measured by qRT-PCR. Effects of miR-506-3p expression on PCa cell behaviors were investigated with MTT assay, colony formation assay, and transwell invasion assay. Connection of miR-506-3p and N-Acetylgalactosaminyltransferase-4 (GALNT4) was analyzed with luciferase activity reporter assay and Western blot assay.miR-506-3p expression was downregulated in PCa cell lines. Function studies demonstrated that overexpression of miR-506-3p inhibits PCa tumor progression in vitro. Mechanistic investigations found GALNT4 was a direct target of miR-506-3p. Overexpression of GALNT4 reversed the tumor-suppressive effects of miR-506-3p on PCa cell.Our results elucidated genetic silencing of miR-506-3p enhances GALNT4 oncogene expression to accelerate PCa progression.
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