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The realisation of targeted antitumour therapy
Better understanding of the pathways regulating proliferation and metastasis of cancer cells has led to the development of novel molecular-targeted therapies. The number of molecular-targeted agents approved for use in the clinic is growing, with many more in clinical trials. Most of these compounds...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362059/ https://www.ncbi.nlm.nih.gov/pubmed/15928654 http://dx.doi.org/10.1038/sj.bjc.6602602 |
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author | Bicknell, R |
author_facet | Bicknell, R |
author_sort | Bicknell, R |
collection | PubMed |
description | Better understanding of the pathways regulating proliferation and metastasis of cancer cells has led to the development of novel molecular-targeted therapies. The number of molecular-targeted agents approved for use in the clinic is growing, with many more in clinical trials. Most of these compounds can be broadly classified into two main categories: monoclonal antibodies and small-molecule tyrosine kinase inhibitors. The pathological processes targeted include vascular endothelial growth factor-dependent tumour angiogenesis and epidermal growth factor receptor-dependent tumour cell proliferation and survival. Unlike conventional chemotherapy, molecular-targeted agents offer the potential advantages of a relatively high therapeutic window and use in combination with other anticancer strategies without overlapping toxicity. It is hoped that these drugs will become valuable therapeutic tools within the multimodal approach to treating cancer. Recent progress in targeted antitumour therapy is discussed, with a focus on antiangiogenesis. |
format | Text |
id | pubmed-2362059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23620592009-09-10 The realisation of targeted antitumour therapy Bicknell, R Br J Cancer Original Article Better understanding of the pathways regulating proliferation and metastasis of cancer cells has led to the development of novel molecular-targeted therapies. The number of molecular-targeted agents approved for use in the clinic is growing, with many more in clinical trials. Most of these compounds can be broadly classified into two main categories: monoclonal antibodies and small-molecule tyrosine kinase inhibitors. The pathological processes targeted include vascular endothelial growth factor-dependent tumour angiogenesis and epidermal growth factor receptor-dependent tumour cell proliferation and survival. Unlike conventional chemotherapy, molecular-targeted agents offer the potential advantages of a relatively high therapeutic window and use in combination with other anticancer strategies without overlapping toxicity. It is hoped that these drugs will become valuable therapeutic tools within the multimodal approach to treating cancer. Recent progress in targeted antitumour therapy is discussed, with a focus on antiangiogenesis. Nature Publishing Group 2005-06 2005-05-31 /pmc/articles/PMC2362059/ /pubmed/15928654 http://dx.doi.org/10.1038/sj.bjc.6602602 Text en Copyright © 2005 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 | Original Article Bicknell, R The realisation of targeted antitumour therapy |
title | The realisation of targeted antitumour therapy |
title_full | The realisation of targeted antitumour therapy |
title_fullStr | The realisation of targeted antitumour therapy |
title_full_unstemmed | The realisation of targeted antitumour therapy |
title_short | The realisation of targeted antitumour therapy |
title_sort | realisation of targeted antitumour therapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362059/ https://www.ncbi.nlm.nih.gov/pubmed/15928654 http://dx.doi.org/10.1038/sj.bjc.6602602 |
work_keys_str_mv | AT bicknellr therealisationoftargetedantitumourtherapy AT bicknellr realisationoftargetedantitumourtherapy |