Epiregulin expression by Ets-1 and ERK signaling pathway in Ki-ras-transformed cells

被引:22
作者
Cho, Min-Chul [1 ]
Choi, Hee-Sook [1 ]
Lee, Sojung [1 ]
Kim, Bo Yeon [2 ]
Jung, Mira [3 ]
Park, Sue Nie [4 ]
Yoon, Do-Young [1 ]
机构
[1] Konkuk Univ, Dept Biosci & Biotechnol, Seoul 143701, South Korea
[2] KRIBB, Lab Cellular Signaling Modulators, Taejon 305333, South Korea
[3] Georgetown Univ, Sch Med, Dept Radiat Med, Washington, DC 20057 USA
[4] Korea Food & Drug Adm, NITR, Div Genet Toxicol, Seoul 122704, South Korea
关键词
Epiregulin; Prosate cancer; Ki-ras; Oncogene; RAF/MEK/ERK pathway; Ets-1;
D O I
10.1016/j.bbrc.2008.10.053
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epiregulin belongs to the epidermal growth factor family. binds to the epidermal growth factor receptor, and its expression is upregulated in various cancer cells, but tire regulatory mechanism is unclear. We investigated the regulatory mechanism of epiregulin expression in Ki-ras-transformed cancer cells. In 267B1/Ki-ras cells, the RAF/MEK/ERK pathway was constitutively activated, epiregulin was up-regulated, and the expression and phosphorylation of Ets-1 were augmented. The inhibition of ERK by PD98059 decreased epiregulin and Ets-1 expression and Suppressed the growth of 267B1/Ki-ras cells. A chromatin immunoprecipitation assay demonstrated that Ets-1 was bound to human epiregulin promoter, and this binding was abolished by PD98059. Silencing of Ets-1 by RNA interference decreased cellular epiregulin transcript expression. We suggest that the Ki-ras mutation in 267B1 prostate cells constitutively activates the RAF/MEK/ERK pathway and induces the activation of the Ets-1 transcription factor, ultimately leading to the increased expression of epiregulin. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:832 / 837
页数:6
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