| Literature DB >> 25433291 |
Dong Li1, Yu Liu1, Hua Li1, Jing-Jing Peng1, Yan Tan2, Qiang Zou3, Xiao-Feng Song4, Min Du1, Zheng-Hui Yang5, Yong Tan1, Jin-Jun Zhou1, Tao Xu1, Zeng-Qiang Fu1, Jian-Qiong Feng1, Peng Cheng1, Tao chen1, Dong Wei1, Xiao-Mei Su1, Huan-Yi Liu1, Zhong-Chun Qi1, Li-Jun Tang6, Tao Wang6, Xin Guo7, Yong-He Hu8, Tao Zhang9.
Abstract
Although microRNA-1 (miR-1) is a known liver cancer suppressor, the role of miR-1 in apoptosis of hepatoma cells has remained largely unknown. Our study shows that ectopic miR-1 overexpression induced apoptosis of liver hepatocellular carcinoma (HepG2) cells. Apoptosis inhibitor 5 (API-5) was found to be a potential regulator of miR-1 induced apoptosis, using a bioinformatics approach. Furthermore, an inverse relationship between miR-1 and API-5 expression was observed in human liver cancer tissues and adjacent normal liver tissues. Negative regulation of API-5 expression by miR-1 was demonstrated to promote apoptosis of HepG2 cells. Our study provides a novel regulatory mechanism of miR-1 in the apoptosis of hepatoma cells.Entities:
Keywords: Apoptosis; Apoptosis inhibitor 5; Hepatocellular carcinoma; Hepatoma cell; microRNA-1
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Year: 2014 PMID: 25433291 DOI: 10.1016/j.febslet.2014.11.025
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124