Interactome Analysis Reveals that C1QBP (complement component 1, q subcomponent binding protein) Is Associated with Cancer Cell Chemotaxis and Metastasis

被引:51
|
作者
Zhang, Xiaofang [1 ,2 ]
Zhang, Fei [2 ]
Guo, Lin [2 ]
Wang, Yanping [1 ]
Zhang, Peng [2 ]
Wang, Ruirui [1 ]
Zhang, Ning [1 ,2 ]
Chen, Ruibing [1 ]
机构
[1] Tianjin Med Univ, Res Ctr Basic Med Sci, Tianjin 300070, Peoples R China
[2] Tianjin Med Univ, Canc Inst & Hosp, Canc Cell Biol Lab, Key Lab Breast Canc Prevent & Therapy, Tianjin 300070, Peoples R China
基金
中国国家自然科学基金;
关键词
KINASE-C-ZETA; P-32; PROTEIN; GLOBULAR HEADS; RNA-BINDING; PKC-ZETA; EXPRESSION; CDC42; LOCALIZATION; ACTIVATION; REGULATOR;
D O I
10.1074/mcp.M113.029413
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The complement component 1, q subcomponent binding protein (C1QBP/p32/HABP1) is a ubiquitously expressed and multicompartmental cellular protein involved in various biological processes. In order to further understand its biological functions, we conducted proteomics analysis of its interactome in this study. An improved sample preparation and mass spectrometric identification strategy was developed combining high-speed centrifugation, formaldehyde labeling, and two-dimensional reverse-phase liquid chromatography. Using this approach, we identified 187 interacting proteins and constructed a highly connected interacting network for C1QBP. Moreover, we explored the interaction between C1QBP and protein kinase C , a key regulator of cell polarity and migration. The results indicated that C1QBP regulated the activity of protein kinase C and modulated EGF-induced cancer cell chemotaxis. In addition, C1QBP was required for breast cancer metastasis in a severe combined immunodeficiency mouse model. Furthermore, C1QBP was observed to be overexpressed in breast cancer tissues, and its expression level was closely linked with distant metastasis and TNM stages. In summary, C1QBP was identified as a novel regulator of cancer metastasis that may serve as a therapeutic target for breast cancer treatment. Molecular & Cellular Proteomics 12: 10.1074/mcp.M113.029413, 3199-3209, 2013.
引用
收藏
页码:3199 / 3209
页数:11
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