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Cancer treatment with kinase inhibitors: what have we learnt from imatinib?

Over the past few years, a number of anticancer drugs have been developed that specifically target kinases known to be oncogenic. The leading drug in this area is imatinib mesylate, which targets ABL, KIT and PDGFR. It has been remarkably effective in the treatment of chronic myeloid leukaemia, alth...

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Detalles Bibliográficos
Autores principales: Ross, D M, Hughes, T P
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395307/
https://www.ncbi.nlm.nih.gov/pubmed/14710199
http://dx.doi.org/10.1038/sj.bjc.6601507
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author Ross, D M
Hughes, T P
author_facet Ross, D M
Hughes, T P
author_sort Ross, D M
collection PubMed
description Over the past few years, a number of anticancer drugs have been developed that specifically target kinases known to be oncogenic. The leading drug in this area is imatinib mesylate, which targets ABL, KIT and PDGFR. It has been remarkably effective in the treatment of chronic myeloid leukaemia, although resistance remains a significant problem. From the imatinib experience in this setting, we present some principles of kinase inhibition that may have more general applicability in targeted anticancer therapy. It is clear that the identification of appropriate targets (activated kinases) and monitoring levels of response (to recognise emerging resistance) are essential to optimise clinical management.
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spelling pubmed-23953072009-09-10 Cancer treatment with kinase inhibitors: what have we learnt from imatinib? Ross, D M Hughes, T P Br J Cancer Minireview Over the past few years, a number of anticancer drugs have been developed that specifically target kinases known to be oncogenic. The leading drug in this area is imatinib mesylate, which targets ABL, KIT and PDGFR. It has been remarkably effective in the treatment of chronic myeloid leukaemia, although resistance remains a significant problem. From the imatinib experience in this setting, we present some principles of kinase inhibition that may have more general applicability in targeted anticancer therapy. It is clear that the identification of appropriate targets (activated kinases) and monitoring levels of response (to recognise emerging resistance) are essential to optimise clinical management. Nature Publishing Group 2004-01-12 2004-01-06 /pmc/articles/PMC2395307/ /pubmed/14710199 http://dx.doi.org/10.1038/sj.bjc.6601507 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Minireview
Ross, D M
Hughes, T P
Cancer treatment with kinase inhibitors: what have we learnt from imatinib?
title Cancer treatment with kinase inhibitors: what have we learnt from imatinib?
title_full Cancer treatment with kinase inhibitors: what have we learnt from imatinib?
title_fullStr Cancer treatment with kinase inhibitors: what have we learnt from imatinib?
title_full_unstemmed Cancer treatment with kinase inhibitors: what have we learnt from imatinib?
title_short Cancer treatment with kinase inhibitors: what have we learnt from imatinib?
title_sort cancer treatment with kinase inhibitors: what have we learnt from imatinib?
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395307/
https://www.ncbi.nlm.nih.gov/pubmed/14710199
http://dx.doi.org/10.1038/sj.bjc.6601507
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