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Regulation of Src Family Kinases in Human Cancers

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 thr...

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Detalles Bibliográficos
Autores principales: Sen, Banibrata, Johnson, Faye M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135246/
https://www.ncbi.nlm.nih.gov/pubmed/21776389
http://dx.doi.org/10.1155/2011/865819
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author Sen, Banibrata
Johnson, Faye M.
author_facet Sen, Banibrata
Johnson, Faye M.
author_sort Sen, Banibrata
collection PubMed
description 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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spelling pubmed-31352462011-07-20 Regulation of Src Family Kinases in Human Cancers Sen, Banibrata Johnson, Faye M. J Signal Transduct Review Article 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. Hindawi Publishing Corporation 2011 2011-04-04 /pmc/articles/PMC3135246/ /pubmed/21776389 http://dx.doi.org/10.1155/2011/865819 Text en Copyright © 2011 B. Sen and F. M. Johnson. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Sen, Banibrata
Johnson, Faye M.
Regulation of Src Family Kinases in Human Cancers
title Regulation of Src Family Kinases in Human Cancers
title_full Regulation of Src Family Kinases in Human Cancers
title_fullStr Regulation of Src Family Kinases in Human Cancers
title_full_unstemmed Regulation of Src Family Kinases in Human Cancers
title_short Regulation of Src Family Kinases in Human Cancers
title_sort regulation of src family kinases in human cancers
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135246/
https://www.ncbi.nlm.nih.gov/pubmed/21776389
http://dx.doi.org/10.1155/2011/865819
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