基因敲除
运行x2
转录因子
癌症研究
生物
基因表达
细胞周期
癌细胞
细胞培养
分子生物学
细胞
癌症
基因
遗传学
作者
M. Gokulnath,Nicola C. Partridge,N. Selvamurugan
出处
期刊:Tumor Biology
[SAGE Publishing]
日期:2014-11-08
卷期号:36 (3): 1923-1931
被引量:33
标识
DOI:10.1007/s13277-014-2796-x
摘要
Activating transcription factor (ATF-3) is a stress response gene and is induced by transforming growth factor beta 1 (TGF-β1) in breast cancer cells. In this study, we dissected the functional role of ATF-3 gene in vitro by knocking down its expression stably in human bone metastatic breast cancer cells (MDA-MB231). Knockdown of ATF-3 expression in these cells decreased cell number, altered cell cycle phase transition, and decreased mRNA expression of cell cycle genes. Knockdown of ATF-3 expression in MDA-MB231 cells also decreased cell migration, and the expression levels of invasive and metastatic genes such as MMP-13 and Runx2 were found to be decreased in these cells. Most importantly, ATF-3 was associated with Runx2 promoter in MDA-MB231 cells and knockdown of ATF-3 expression decreased its association with Runx2 promoter. Hence, our results suggested that ATF-3 plays a role in proliferation and invasion of bone metastatic breast cancer cells in vitro and we identified for the first time that Runx2 is a target gene of ATF-3 in MDA-MB231 cell line.
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