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Regulation of Src Family Kinases in Human Cancers
Author(s) -
Banibrata Sen,
Faye M. Johnson
Publication year - 2011
Publication title -
journal of signal transduction
Language(s) - English
Resource type - Journals
eISSN - 2090-1739
pISSN - 2090-1747
DOI - 10.1155/2011/865819
Subject(s) - proto oncogene tyrosine protein kinase src , tyrosine protein kinase csk , kinase , tyrosine kinase , cancer research , angiogenesis , medicine , cancer , signal transduction , metastasis , receptor tyrosine kinase , sh3 domain , protein kinase domain , src family kinase , microbiology and biotechnology , biology , biochemistry , gene , mutant
The nonreceptor protein tyrosine kinase Src plays a crucial role in the signal transduction pathways involved in cell division, motility, adhesion, and survival in both normal and cancer cells. Although the Src family kinases (SFKs) are activated in various types of cancers, the exact mechanisms through which they contribute to the progression of individual tumors remain to be defined. The activation of Src in human cancers may occur through a variety of mechanisms that include domain interaction and structural remodeling in response to various activators or upstream kinases and phosphatastes. Because of Src's prominent roles in invasion and tumor progression, epithelial-to-mesenchymal transition, angiogenesis, and the development of metastasis, Src is a promising target for cancer therapy. Several small molecule inhibitors of Src are currently being investigated in clinical trials. In this article, we will summarize the mechanisms regulating Src kinase activity in normal and cancer cells and discuss the status of Src inhibitor development against various types of cancers.

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