The mechanism of growth-inhibitory effect of DOC-2/DAB2 in prostate cancer - Characterization of a novel GTPase-activating protein associated with N-terminal domain of DOC-2/DAB2

被引:123
|
作者
Wang, Z
Tseng, CP
Pong, RC
Chen, H
McConnell, JD
Navone, N
Hsieh, JT
机构
[1] Univ Texas, SW Med Ctr, Dept Urol, Dallas, TX 75390 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept GU Med Oncol, Houston, TX 77030 USA
关键词
D O I
10.1074/jbc.M110568200
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
DOC-2/DAB2 is a member of the disable gene family with tumor-inhibitory activity. Its down-regulation is associated with several neoplasms, and serine phosphorylation of its N terminus modulates DOC-2/DAB2's inhibitory effect on AP-1 transcriptional activity. We describe the cloning of DIP1/2, a novel gene that interacts with the N-terminal domain of DOC-2/DAB2. DIP1/2 is a novel GTPase-activating protein containing a Ras GTPase-activating protein homology domain (N terminus) and two other unique domains (i.e. 10 proline repeats and leucine zipper). Interaction between DOC-2/DAB2 and DIP1/2 is detected in normal tissues such as the brain and prostate. Altered expression of these two proteins is often detected in prostate cancer cells. Indeed, the presence of DIP1/2 effectively blocks mitogen-induced gene expression and inhibits the growth of prostate cancer. Thus, DOC-2/DAB2 and DIP1/2 appear to represent a unique negative regulatory complex that maintains cell homeostasis.
引用
收藏
页码:12622 / 12631
页数:10
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