Identification of integrin α1 as an interacting protein of protein tyrosine phosphatase PRL-3

被引:71
作者
Peng, LR [1 ]
Jin, GL [1 ]
Wang, L [1 ]
Guo, JP [1 ]
Meng, L [1 ]
Shou, CC [1 ]
机构
[1] Peking Univ, Sch Oncol, Dept Biochem & Mol Biol, Beijing Canc Hosp & Inst, Beijing 100036, Peoples R China
基金
中国国家自然科学基金;
关键词
protein tyrosine phosphatase PRL-3; integrin; interaction; erk1/2; phosphorylation;
D O I
10.1016/j.bbrc.2006.01.102
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
PRL-3 is a newly identified protein tyrosine phosphatase associated with tumor metastasis. It is over-expressed in various cancers, such as colorectal cancer, gastric cancer, and ovarian cancer, and is correlated with the progression and survival of cancers. Although PRL-3 plays a causative role in promoting cancer cell invasion and metastasis, the molecular mechanism is unknown. To investigate PRL-3's roles in tumorigenesis and signal transduction pathway, we screened the human placenta brain cDNA library with the bait of PRL-3 in yeast two-hybrid system. Then we identified integrin alpha 1 as a PRL-3-interacting protein for the first tinge, and verified this physical association with pull-down and co-immunoprecipitation assays. Furthermore, we found that PRL-3 could down-regulate the tyrosine-phosphorylation level of integrin beta 1 and increased the phosphorylation level of Erk1/2. Our present discovery will provide new cities for elucidating the molecular mechanism of PRL-3 in promoting cancer invasion and metastasis. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:179 / 183
页数:5
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