Interaction of the DF3/MUC1 breast carcinoma-associated antigen and beta-catenin in cell adhesion

被引:283
作者
Yamamoto, M
Bharti, A
Li, YQ
Kufe, D
机构
[1] Division of Cancer Pharmacology, Dana-Farber Cancer Institute, Harvard Medical School, Boston
关键词
D O I
10.1074/jbc.272.19.12492
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
The DF3/MUC1 mucin-like glycoprotein is aberrantly overexpressed in human breast carcinomas. The functional role of DF3 is unknown. The present studies demonstrate that DF3 associates with beta-catenin. Similar findings have been obtained for gamma-catenin but not alpha-catenin. DF3, like E-cadherin and the adenomatous polyposis coli gene product, contains an SXXXXXSSL site that is responsible for direct binding to beta-catenin. The results further demonstrate that interaction of DF3 and beta-catenin is dependent on cell adhesion. These findings and the role of beta-catenin in cell signaling support a role for DF3 in the adhesion of epithelial cells.
引用
收藏
页码:12492 / 12494
页数:3
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