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Par6-aPKC uncouples ErbB2 induced disruption of polarized epithelial organization from proliferation control
被引:196
作者:
Aranda, Victoria
Haire, Teresa
Nolan, Marissa E.
Calarco, Joseph P.
Rosenberg, Avi Z.
Fawcett, James P.
Pawson, Tony
Muthuswamy, Senthil K.
机构:
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] SUNY Stony Brook, Dept Mol Genet & Microbiol, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Grad Program Genet, Stony Brook, NY 11794 USA
[4] Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[5] Univ Toronto, Program Mol Biol & Canc, Samuel Lunenfeld Res Inst, Mt Sinai Hosp, Toronto, ON M5G 1X5, Canada
[6] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
关键词:
D O I:
10.1038/ncb1485
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The polarized glandular organization of epithelial cells is frequently lost during development of carcinoma. However, the specific oncogene targets responsible for polarity disruption have not been identified. Here, we demonstrate that activation of ErbB2 disrupts apical-basal polarity by associating with Par6-aPKC, components of the Par polarity complex. Inhibition of interaction between Par6 and aPKC blocked the ability of ErbB2 to disrupt the acinar organization of breast epithelia and to protect cells from apoptosis but was not required for cell proliferation. Therefore, oncogenes target polarity proteins to disrupt glandular organization and protect cells from apoptotic death during development of carcinoma.
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页码:1235 / U20
页数:14
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