A role for the scaffolding adapter GAB2 in breast cancer

被引:165
作者
Bentires-Alj, M
Gil, SG
Chan, R
Wang, ZGC
Wang, YP
Imanaka, N
Harris, LN
Richardson, A
Neel, BG
Gu, HH
机构
[1] Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Univ Liege, Lab Med Chem & Human Genet, Ctr Biomed Integrat Genoproteom, B-4000 Liege, Belgium
[4] Brigham & Womens Hosp, Dept Surg, Boston, MA 02115 USA
[5] Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1038/nm1341
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 scaffolding adapter GAB2 maps to a region (11q13-14) commonly amplified in human breast cancer, and is overexpressed in breast cancer cell lines and primary tumors, but its functional role in mammary carcinogenesis has remained unexplored. We found that overexpression of GAB2 (Grb2-associated binding protein 2) increases proliferation of MCF10A mammary cells in three-dimensional culture. Coexpression of GAB2 with antiapoptotic oncogenes causes lumenal filling, whereas coexpression with Neu (also known as ErbB2 and HER2) results in an invasive phenotype. These effects of GAB2 are mediated by hyperactivation of the Shp2-Erk pathway. Furthermore, overexpression of Gab2 potentiates, whereas deficiency of Gab2 ameliorates, Neu-evoked breast carcinogenesis in mice. Finally, GAB2 is amplified in some GAB2-overexpressing human breast tumors. Our data suggest that GAB2 may be a key gene within an 11q13 amplicon in human breast cancer and propose a role for overexpression of GAB2 in mammary carcinogenesis. Agents that target GAB2 or GAB2-dependent pathways may be useful for treating breast tumors that overexpress GAB2 or HER2 or both.
引用
收藏
页码:114 / 121
页数:8
相关论文
共 48 条
[21]   The 'Gab' in signal transduction [J].
Gu, HH ;
Neel, BG .
TRENDS IN CELL BIOLOGY, 2003, 13 (03) :122-130
[22]   Cloning of p97/Gab2, the major SHP2-binding protein in hematopoietic cells, reveals a novel pathway for cytokine-induced gene activation [J].
Gu, HH ;
Pratt, JC ;
Burakoff, SJ ;
Neel, BG .
MOLECULAR CELL, 1998, 2 (06) :729-740
[23]   Gene expression predictors of breast cancer outcomes [J].
Huang, E ;
Cheng, SH ;
Dressman, H ;
Pittman, J ;
Tsou, MH ;
Horng, CF ;
Bild, A ;
Iversen, ES ;
Liao, M ;
Chen, CM ;
West, M ;
Nevins, JR ;
Huang, AT .
LANCET, 2003, 361 (9369) :1590-1596
[24]   Scaffolding protein Gab2 mediates fibroblast transformation by the SEA tyrosine kinase [J].
Ischenko, I ;
Petrenko, O ;
Gu, HH ;
Hayman, MJ .
ONCOGENE, 2003, 22 (41) :6311-6318
[25]   Epidermal growth factor-induced DNA synthesis - Key role for Src phosphorylation of the docking protein Gab2 [J].
Kong, M ;
Mounier, C ;
Dumas, V ;
Posner, BI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :5837-5844
[26]   The gift of gab [J].
Liu, Y ;
Rohrschneider, LR .
FEBS LETTERS, 2002, 515 (1-3) :1-7
[27]   Identification of an atypical Grb2 carboxyl-terminal SH3 domain binding site in Gab docking proteins reveals Grb2-dependent and -independent recruitment of Gab1 to receptor tyrosine kinases [J].
Lock, LS ;
Royal, I ;
Naujokas, MA ;
Park, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (40) :31536-31545
[28]   BRCA1 promoter methylation in sporadic breast tumors: relationship to gene expression profiles [J].
Matros, E ;
Wang, ZGC ;
Lodeiro, G ;
Miron, A ;
Iglehart, JD ;
Richardson, AL .
BREAST CANCER RESEARCH AND TREATMENT, 2005, 91 (02) :179-186
[29]   Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is required for induction of autophagy during lumen formation in vitro [J].
Mills, KR ;
Reginato, M ;
Debnath, J ;
Queenan, B ;
Brugge, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (10) :3438-3443
[30]   Prognostic, therapeutic, and mechanistic implications of a mouse model of leukemia evoked by Shp2 (PTPN11) mutations [J].
Mohi, MG ;
Williams, IR ;
Dearolf, CR ;
Chan, G ;
Kutok, JL ;
Cohen, S ;
Morgan, K ;
Boulton, C ;
Shigematsu, H ;
Keilhack, H ;
Akashi, K ;
Gilliland, DG ;
Neel, BG .
CANCER CELL, 2005, 7 (02) :179-191