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Co‐regulation of B‐Myb expression by E2F1 and EGF receptor
Author(s) -
Hanada Norihisa,
Lo HuiWen,
Day ChiPing,
Pan Yong,
Nakajima Yusuke,
Hung MienChie
Publication year - 2005
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/mc.20147
Subject(s) - biology , e2f1 , cancer research , myb , transcription factor , epidermal growth factor receptor , microbiology and biotechnology , receptor , gene , genetics
Abstract Epidermal growth factor receptor (EGFR) is a receptor tyrosine kinase that is frequently over‐expressed in human cancers and is associated with tumorigenesis, and increased tumor proliferation and progression. Also found in breast tumors with high levels is B‐Myb, a transcription factor whose expression is activated by E2F1/3 at the late G 1 phase and the level is sustained through the S phase. Recent reports suggest a casual correlation between EGFR and B‐Myb expression in primary breast carcinomas. However, the mechanism for such co‐expression remains un‐investigated. Here, we report that EGFR is important for B‐Myb expression and the underlying mechanism involves cooperated effects from EGFR and E2F1. EGF stimulation and forced expression of EGFR significantly increase B‐Myb gene activity and such increase occurs in the G 1 phase. EGF‐induced B‐Myb expression was not significantly suppressed following inhibition of PI‐3K and ERK, two major EGFR downstream pathways. In contrast, we observed EGF‐induced in vivo association of nuclear EGFR to the B‐Myb promoter and the association is only detected at the G 1 /S phase and is abolished by EGFR kinase inhibitor. As EGFR lacks DNA‐binding domain but contains transactivational activity and E2F1 activates B‐Myb expression in the G 1 /S phase, we further reasoned that nuclear EGFR might cooperate with E2F1 leading to activation of B‐Myb. Indeed, we found that EGFR co‐immunoprecipitated with E2F1 in an EGF‐dependent manner and that EGF activated in vivo binding of E2F1 to the B‐Myb promoter. Consistently, forced expression of both EGFR and E2F1 in EGFR‐null CHO cells greatly enhanced B‐Myb promoter activity, compared to the vector control and expression of EGFR or E2F1 alone. Promoter mutagenesis studies showed that EGF‐induced activation of B‐Myb promoter required both E2F and EGFR target sites. In summary, our data suggest that deregulated EGFR signaling pathway facilitate tumor cell proliferation partly via EGFR interaction with E2F1 and subsequent activation of B‐Myb gene expression. © 2005 Wiley‐Liss, Inc.