| Literature DB >> 19697322 |
Hyun Hee Lee1, Young Joon Son1, Won Hyeok Lee1, Young Woo Park2, Seoung Wan Chae3, Wha Ja Cho4, Young Min Kim5, Hye-Jeong Choi5, Dae Hwa Choi6, Seok Won Jung7, Young Joo Min4,7, Soon Eun Park8, Byung Ju Lee1,4, Hee Jeong Cha5, Jeong Woo Park1,4.
Abstract
Tristetraprolin (TTP) is an AU-rich element-binding protein that regulates mRNA stability. Here, we report that TTP suppress the growth of human colon cancer cells both in vivo and in vitro by regulating of the expression of vascular endothelial growth factor (VEGF). TTP protein expression in human colonic tissues was markedly decreased in colonic adenocarcinoma compared with in normal mucosa and adenoma. VEGF expression was higher in colonic adenocarcinoma than in normal mucosa and adenoma. Specific inhibition of TTP expression by RNA-interference increased the expression of VEGF in cultured human colon cancer cells, and TTP overexpression markedly decreased it. In addition, elevated expression of TTP decreased the expression level of luciferase linked to a 3' terminal AU-rich element (ARE) of VEGF mRNA. Colo320/TTP cells overexpressing TTP grew slowly in vitro and became tumors small in size when xenografted s.c into nude mice. These findings demonstrate that TTP acts as a negative regulator of VEGF gene expression in colon cancer cells, suggesting that it can be used as novel therapeutic agent to treat colon cancer.Entities:
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Year: 2010 PMID: 19697322 DOI: 10.1002/ijc.24847
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396