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A framework for the development of effective anti-metastatic agents
Most cancer-related deaths are a result of metastasis, and thus the importance of this process as a target of therapy cannot be understated. By asking ‘how can we effectively treat cancer?’, we do not capture the complexity of a disease encompassing >200 different cancer types — many consisting o...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136167/ https://www.ncbi.nlm.nih.gov/pubmed/30514977 http://dx.doi.org/10.1038/s41571-018-0134-8 |
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author | Anderson, Robin L. Balasas, Theo Callaghan, Juliana Coombes, R. Charles Evans, Jeff Hall, Jacqueline A. Kinrade, Sally Jones, David Jones, Paul S. Jones, Rob Marshall, John F. Panico, Maria Beatrice Shaw, Jacqui A. Steeg, Patricia S. Sullivan, Mark Tong, Warwick Westwell, Andrew D. Ritchie, James W. A. |
author_facet | Anderson, Robin L. Balasas, Theo Callaghan, Juliana Coombes, R. Charles Evans, Jeff Hall, Jacqueline A. Kinrade, Sally Jones, David Jones, Paul S. Jones, Rob Marshall, John F. Panico, Maria Beatrice Shaw, Jacqui A. Steeg, Patricia S. Sullivan, Mark Tong, Warwick Westwell, Andrew D. Ritchie, James W. A. |
author_sort | Anderson, Robin L. |
collection | PubMed |
description | Most cancer-related deaths are a result of metastasis, and thus the importance of this process as a target of therapy cannot be understated. By asking ‘how can we effectively treat cancer?’, we do not capture the complexity of a disease encompassing >200 different cancer types — many consisting of multiple subtypes — with considerable intratumoural heterogeneity, which can result in variable responses to a specific therapy. Moreover, we have much less information on the pathophysiological characteristics of metastases than is available for the primary tumour. Most disseminated tumour cells that arrive in distant tissues, surrounded by unfamiliar cells and a foreign microenvironment, are likely to die; however, those that survive can generate metastatic tumours with a markedly different biology from that of the primary tumour. To treat metastasis effectively, we must inhibit fundamental metastatic processes and develop specific preclinical and clinical strategies that do not rely on primary tumour responses. To address this crucial issue, Cancer Research UK and Cancer Therapeutics CRC Australia formed a Metastasis Working Group with representatives from not-for-profit, academic, government, industry and regulatory bodies in order to develop recommendations on how to tackle the challenges associated with treating (micro)metastatic disease. Herein, we describe the challenges identified as well as the proposed approaches for discovering and developing anticancer agents designed specifically to prevent or delay the metastatic outgrowth of cancer. |
format | Online Article Text |
id | pubmed-7136167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71361672020-04-08 A framework for the development of effective anti-metastatic agents Anderson, Robin L. Balasas, Theo Callaghan, Juliana Coombes, R. Charles Evans, Jeff Hall, Jacqueline A. Kinrade, Sally Jones, David Jones, Paul S. Jones, Rob Marshall, John F. Panico, Maria Beatrice Shaw, Jacqui A. Steeg, Patricia S. Sullivan, Mark Tong, Warwick Westwell, Andrew D. Ritchie, James W. A. Nat Rev Clin Oncol Consensus Statement Most cancer-related deaths are a result of metastasis, and thus the importance of this process as a target of therapy cannot be understated. By asking ‘how can we effectively treat cancer?’, we do not capture the complexity of a disease encompassing >200 different cancer types — many consisting of multiple subtypes — with considerable intratumoural heterogeneity, which can result in variable responses to a specific therapy. Moreover, we have much less information on the pathophysiological characteristics of metastases than is available for the primary tumour. Most disseminated tumour cells that arrive in distant tissues, surrounded by unfamiliar cells and a foreign microenvironment, are likely to die; however, those that survive can generate metastatic tumours with a markedly different biology from that of the primary tumour. To treat metastasis effectively, we must inhibit fundamental metastatic processes and develop specific preclinical and clinical strategies that do not rely on primary tumour responses. To address this crucial issue, Cancer Research UK and Cancer Therapeutics CRC Australia formed a Metastasis Working Group with representatives from not-for-profit, academic, government, industry and regulatory bodies in order to develop recommendations on how to tackle the challenges associated with treating (micro)metastatic disease. Herein, we describe the challenges identified as well as the proposed approaches for discovering and developing anticancer agents designed specifically to prevent or delay the metastatic outgrowth of cancer. Nature Publishing Group UK 2018-12-04 2019 /pmc/articles/PMC7136167/ /pubmed/30514977 http://dx.doi.org/10.1038/s41571-018-0134-8 Text en © Springer Nature Limited 2018 Open Access 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 http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Consensus Statement Anderson, Robin L. Balasas, Theo Callaghan, Juliana Coombes, R. Charles Evans, Jeff Hall, Jacqueline A. Kinrade, Sally Jones, David Jones, Paul S. Jones, Rob Marshall, John F. Panico, Maria Beatrice Shaw, Jacqui A. Steeg, Patricia S. Sullivan, Mark Tong, Warwick Westwell, Andrew D. Ritchie, James W. A. A framework for the development of effective anti-metastatic agents |
title | A framework for the development of effective anti-metastatic agents |
title_full | A framework for the development of effective anti-metastatic agents |
title_fullStr | A framework for the development of effective anti-metastatic agents |
title_full_unstemmed | A framework for the development of effective anti-metastatic agents |
title_short | A framework for the development of effective anti-metastatic agents |
title_sort | framework for the development of effective anti-metastatic agents |
topic | Consensus Statement |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136167/ https://www.ncbi.nlm.nih.gov/pubmed/30514977 http://dx.doi.org/10.1038/s41571-018-0134-8 |
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