Abstract
The rationale to target receptor protein tyrosine kinases (RPTKs) as an approach to cancer chemotherapy has continued to become more compelling with time. Preclinical and clinical data strongly support the involvement of specific RPTKs in the formation and progression of a subset of solid and liquid tumors. The advances in our understanding of the oncogenic activation of these receptors have been matched by the identification of new structural classes of kinase inhibitors that exhibit enormous improvements with regard to potency, specificity and efficacy. This article summarizes current knowledge of the most promising RPTK inhibitors in clinical trials or known to be in late stage preclinical development.
Keywords: angiogenesis, cancer therapy, signal transduction inhibitors, signaling pathways
Mini-Reviews in Medicinal Chemistry
Title: Therapeutically Targeted Anticancer Agents: Inhibitors of Receptor Tyrosine Kinases
Volume: 4 Issue: 3
Author(s): Carlos Garcia-Echeverria and Doriano Fabbro
Affiliation:
Keywords: angiogenesis, cancer therapy, signal transduction inhibitors, signaling pathways
Abstract: The rationale to target receptor protein tyrosine kinases (RPTKs) as an approach to cancer chemotherapy has continued to become more compelling with time. Preclinical and clinical data strongly support the involvement of specific RPTKs in the formation and progression of a subset of solid and liquid tumors. The advances in our understanding of the oncogenic activation of these receptors have been matched by the identification of new structural classes of kinase inhibitors that exhibit enormous improvements with regard to potency, specificity and efficacy. This article summarizes current knowledge of the most promising RPTK inhibitors in clinical trials or known to be in late stage preclinical development.
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Cite this article as:
Garcia-Echeverria Carlos and Fabbro Doriano, Therapeutically Targeted Anticancer Agents: Inhibitors of Receptor Tyrosine Kinases, Mini-Reviews in Medicinal Chemistry 2004; 4 (3) . https://dx.doi.org/10.2174/1389557043487349
DOI https://dx.doi.org/10.2174/1389557043487349 |
Print ISSN 1389-5575 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5607 |
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