六氯环己烷
AKT3
癌变
癌症研究
和平号-122
小RNA
生物
肝细胞癌
细胞生长
细胞凋亡
癌症
遗传学
PI3K/AKT/mTOR通路
基因
AKT1型
作者
Rounak Nassirpour,Pramod P. Mehta,Min-Jean Yin
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2013-11-07
卷期号:8 (11): e79655-e79655
被引量:89
标识
DOI:10.1371/journal.pone.0079655
摘要
MicroRNAs (miRNAs) have been implicated in the orchestration of diverse cellular processes including differentiation, proliferation, and apoptosis and are believed to play pivotal roles as oncogenes and tumor suppressors. miR-122, a liver specific miRNA, is significantly down-regulated in most hepatocellular carcinomas (HCCs) but its role in tumorigenesis remains poorly understood. Here we identify AKT3 as a novel and direct target of miR-122. Restoration of miR-122 expression in HCC cell lines decreases AKT3 levels, inhibits cell migration and proliferation, and induces apoptosis. These anti-tumor phenotypes can be rescued by reconstitution of AKT3 expression indicating the essential role of AKT3 in miR-122 mediated HCC transformation. In vivo, restoration of miR-122 completely inhibited xenograft growth of HCC tumor in mice. Our data strongly suggest that miR-122 is a tumor suppressor that targets AKT3 to regulate tumorigenesis in HCCs and a potential therapeutic candidate for liver cancer.
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