Cellular transformation by Simian Virus 40 and Murine Polyoma Virus T antigens

被引:118
|
作者
Cheng, Jingwei [1 ,2 ,3 ]
DeCaprio, James A. [1 ,2 ,3 ,4 ]
Fluck, Michele M. [5 ]
Schaffhausen, Brian S. [6 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Ctr Appl Canc Sci, Boston, MA 02115 USA
[5] Michigan State Univ, Interdept Program Cell & Mol Biol, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
[6] Tufts Univ, Sch Med, Dept Biochem, Boston, MA 02111 USA
关键词
SV40; Polyoma; T antigen; p53; Retinoblastoma; Src; PI3; kinase; Shc; RETINOBLASTOMA TUMOR-SUPPRESSOR; PROTEIN PHOSPHATASE 2A; INSULIN-RECEPTOR SUBSTRATE-1; PRB-RELATED PROTEINS; MIDDLE-T; MAMMARY-TUMORS; MEDIATED TRANSFORMATION; PHOSPHATIDYLINOSITOL; 3-KINASE; TRANSGENIC MICE; SIMIAN VIRUS-40;
D O I
10.1016/j.semcancer.2009.03.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simian Virus 40 (SV40) and Mouse Polyoma Virus (PY) are small DNA tumor viruses that have been used extensively to study cellular transformation. The SV40 early region encodes three tumor antigens, large T (LT), small T (ST) and 17KT that contribute to cellular transformation. While PY also encodes LT and ST, the unique middle T (MT) generates most of the transforming activity. SV40 IT mediated transformation requires binding to the tumor suppressor proteins Rb and p53 in the nucleus and ST binding to the protein phosphatase PP2A in the cytoplasm. SV40 IT also binds to several additional cellular proteins including p300, CBP, Cul7, IRS1, Bub1, Nbs1 and Fbxw7 that contribute to viral transformation. PY MT transformation is dependent on binding to PP2A and the Src family protein tyrosine kinases (PTK) and assembly of a signaling complex on cell membranes that leads to transformation in a manner similar to Her2/neu. Phosphorylation of MT tyrosine residues activates key signaling molecules including Shc/Grb2, PI3K and PLC gamma 1. The unique contributions of SV40 LT and ST and PY MT to cellular transformation have provided significant insights into our understanding of tumor suppressors, oncogenes and the process of oncogenesis. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:218 / 228
页数:11
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