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Divide and Conquer: Progress in the Molecular Stratification of Cancer

Cancer remains an outstanding cause of global morbidity and mortality, despite intensive research and unprecedented insights into the basic mechanisms of cancer development. A plethora of clinical and experimental evidence suggests that cancers from individual patients are likely to be molecularly h...

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Detalles Bibliográficos
Autor principal: Tan, Patrick
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2730607/
https://www.ncbi.nlm.nih.gov/pubmed/19718393
http://dx.doi.org/10.3349/ymj.2009.50.4.464
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author Tan, Patrick
author_facet Tan, Patrick
author_sort Tan, Patrick
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description Cancer remains an outstanding cause of global morbidity and mortality, despite intensive research and unprecedented insights into the basic mechanisms of cancer development. A plethora of clinical and experimental evidence suggests that cancers from individual patients are likely to be molecularly heterogeneous in their use of distinct oncogenic pathways and biological programs. Efforts to significantly impact cancer patient outcomes will almost certainly require the development of robust strategies to subdivide such heterogeneous panels of cancers into biologically and clinically homogenous subgroups, for the purposes of personalizing treatment protocols and identifying optimal drug targets. In this review, I describe recent progress in the development of both targeted and genome-wide approaches for the molecular stratification of cancers, drawing examples from both the haematopoietic and solid tumor malignancies.
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spelling pubmed-27306072009-08-31 Divide and Conquer: Progress in the Molecular Stratification of Cancer Tan, Patrick Yonsei Med J Review Article Cancer remains an outstanding cause of global morbidity and mortality, despite intensive research and unprecedented insights into the basic mechanisms of cancer development. A plethora of clinical and experimental evidence suggests that cancers from individual patients are likely to be molecularly heterogeneous in their use of distinct oncogenic pathways and biological programs. Efforts to significantly impact cancer patient outcomes will almost certainly require the development of robust strategies to subdivide such heterogeneous panels of cancers into biologically and clinically homogenous subgroups, for the purposes of personalizing treatment protocols and identifying optimal drug targets. In this review, I describe recent progress in the development of both targeted and genome-wide approaches for the molecular stratification of cancers, drawing examples from both the haematopoietic and solid tumor malignancies. Yonsei University College of Medicine 2009-08-31 2009-08-19 /pmc/articles/PMC2730607/ /pubmed/19718393 http://dx.doi.org/10.3349/ymj.2009.50.4.464 Text en © Copyright: Yonsei University College of Medicine 2009 http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Tan, Patrick
Divide and Conquer: Progress in the Molecular Stratification of Cancer
title Divide and Conquer: Progress in the Molecular Stratification of Cancer
title_full Divide and Conquer: Progress in the Molecular Stratification of Cancer
title_fullStr Divide and Conquer: Progress in the Molecular Stratification of Cancer
title_full_unstemmed Divide and Conquer: Progress in the Molecular Stratification of Cancer
title_short Divide and Conquer: Progress in the Molecular Stratification of Cancer
title_sort divide and conquer: progress in the molecular stratification of cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2730607/
https://www.ncbi.nlm.nih.gov/pubmed/19718393
http://dx.doi.org/10.3349/ymj.2009.50.4.464
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