Src Family Kinases: Potential Targets for the Treatment of Human Cancer and Leukemia

Author(s): Markus Warmuth, Robert Damoiseaux, Yi Liu, Doriano Fabbro, Nathanael Gray.

Journal Name: Current Pharmaceutical Design

Volume 9 , Issue 25 , 2003

Submit Manuscript
Submit Proposal

Abstract:

The inherited or acquired deregulation of protein kinase activity has been implicated in the pathogenesis of many human diseases, including cancer. Therefore, the inhibition of kinases has been proposed to be a promising strategy in the context of anti-cancer treatment. Many other kinases have been selected as drug discovery targets based on the prevalence of mutations, over-expression and unscheduled activation in human cancer. Of the various protein kinases chosen, Src family kinases are amongst the most extensively studied kinase oncogenes in academia and industry. This review focuses on our current understanding of the deregulation and role of Src family kinases in human cancer and leukemia. Recent data implicate the action of c-Src in cancer metastasis, mediated by up-regulation of various protease systems (calpain, uPA) as well as disruption of E-cadherin signalling. Moreover, novel roles of various Src family members in the development of human leukemia have been found. New insights into downstream signalling mechanisms, including the activation of STAT3, PDK1 and Akt, further corroborate the importance of Src family kinases in tumorigenesis and chemoresistance. Despite our rather clear understanding of Src family kinases as pro-oncogenes no Src family kinase inhibitor has entered a clinical trial so far. This review will discuss prerequisites to be fulfilled for clinically targeting c-Src and its homologues using small molecule drugs.

Keywords: protein kinases, src family kinases, small molecule kinase inhibitor, leukemogenesis, cancerogenesis

Rights & PermissionsPrintExport Cite as


Article Details

VOLUME: 9
ISSUE: 25
Year: 2003
Page: [2043 - 2059]
Pages: 17
DOI: 10.2174/1381612033454126
Price: $58

Article Metrics

PDF: 4