Tnk1/Kos1 knockout mice develop spontaneous tumors
Document Type
Article
Abstract
Tnk1/Kos1 is a non-receptor protein tyrosine kinase implicated in negatively regulating cell growth in a mechanism requiring its intrinsic catalytic activity. Tnk1/Kos1 null mice were created by homologous recombination by deleting the catalytic domain. Both Tnk1+/- and Tnk1 -/- mice develop spontaneous tumors, including lymphomas and carcinomas, at high rates [27% (14 of 52) and 43% (12 of 28), respectively]. Tnk1/Kos1 expression is silenced in tumors that develop in Tnk1+/- mice but not in adjacent uninvolved tissue, and silencing occurs in association with Tnk1 promoter hypermethylation. Tissues and murine embryonic fibroblasts derived from Tnk1/Kos1-null mice exhibit proportionally higher levels of basal and epidermal growth factor-stimulated Ras activation that results from increased Ras-guanine exchange factor (GEF) activity. Mechanistically, Tnk1/Kos1 can directly tyrosine phosphorylate growth factor receptor binding protein 2 (Grb2), which promotes disruption of the Grb2-Sos1 complex that mediates growth factor-induced Ras activation, providing dynamic regulation of Ras GEF activity with suppression of Ras. Thus, Tnk1/Kos1 is a tumor suppressor that functions to down-regulate Ras activity. ©2008 American Association for Cancer Research.
Publication Date
11-1-2008
Publication Title
Cancer Research
ISSN
00085472
Volume
68
Issue
21
First Page
8723
Last Page
8732
PubMed ID
18974114
Digital Object Identifier (DOI)
10.1158/0008-5472.CAN-08-1467
Recommended Citation
Hoare, Sarasija; Hoare, Kishalay; Reinhard, Mary K.; Lee, Young J.; Oh, S. Paul; and May, W. Stratford, "Tnk1/Kos1 knockout mice develop spontaneous tumors" (2008). Translational Neuroscience. 693.
https://scholar.barrowneuro.org/neurobiology/693