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HER2/Neu (ErbB2) signaling to Rac1-Pak1 is temporally and spatially modulated by transforming growth factor beta
- Wang, Shizhen Emily;
- Shin, Incheol;
- Wu, Frederick Y.;
- Friedman, David B.;
- Arteaga, Carlos L.
WEB OF SCIENCE
91SCOPUS
98초록
In HER2 (ErbB2)-overexpressing cells, transforming growth factor beta (TGF-beta), via activation of phosphoinositide-3 kinase (PI3K), recruits actin and actinin to HER2, which then colocalizes with Vav2, activated Rac1, and Pak1 at cell protrusions. This results in prolonged Rac1. activation, enhanced motility and invasiveness, Bad phosphorylation, uncoupling of Bad/Bcl-2, and enhanced cell survival. The recruitment of the HER2/Vav2/Rac1/Pak1/actin/actinin complex to lamellipodia was abrogated by actinin siRNAs, dominant-negative (dn) p85, gefitinib, and dn-Rac1 or dnPak1, suggesting that the reciprocal interplay of PI3K, HER2 kinase, and Rac GTPases with the actin cytoskeleton is necessary for TGF-beta action in oncogene-overexpressing cells. Thus, by recruiting the actin skeleton, TGF-beta "cross-links" this signaling complex at cell lamellipodia; this prolongs Rac1 activation and increases metastatic properties and survival of HER2-overexpressing cells.
키워드
- 제목
- HER2/Neu (ErbB2) signaling to Rac1-Pak1 is temporally and spatially modulated by transforming growth factor beta
- 저자
- Wang, Shizhen Emily; Shin, Incheol; Wu, Frederick Y.; Friedman, David B.; Arteaga, Carlos L.
- 발행일
- 2006-10
- 유형
- Article
- 저널명
- Cancer Research
- 권
- 66
- 호
- 19
- 페이지
- 9591 ~ 9600