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Three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells
Recent efforts to understand breast cancer biology involve three interrelated themes that are founded on a combination of clinical and experimental observations. The central concept is gene addiction. The clinical dilemma is the escape from gene addiction, which is mediated, in part, by phenotypic p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262190/ https://www.ncbi.nlm.nih.gov/pubmed/22067349 http://dx.doi.org/10.1186/bcr2887 |
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author | Cardiff, Robert D Couto, Suzana Bolon, Brad |
author_facet | Cardiff, Robert D Couto, Suzana Bolon, Brad |
author_sort | Cardiff, Robert D |
collection | PubMed |
description | Recent efforts to understand breast cancer biology involve three interrelated themes that are founded on a combination of clinical and experimental observations. The central concept is gene addiction. The clinical dilemma is the escape from gene addiction, which is mediated, in part, by phenotypic plasticity as exemplified by epithelial-to-mesenchymal transition and mesenchymal-to-epithelial transition. Finally, cancer stem cells are now recognized as the basis for minimal residual disease and malignant progression over time. These themes cooperate in breast cancer, as induction of epithelial-to-mesenchymal transition enhances self-renewal and expression of cancer stem cells, which are believed to facilitate tumor resistance. |
format | Online Article Text |
id | pubmed-3262190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32621902012-04-25 Three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells Cardiff, Robert D Couto, Suzana Bolon, Brad Breast Cancer Res Review Recent efforts to understand breast cancer biology involve three interrelated themes that are founded on a combination of clinical and experimental observations. The central concept is gene addiction. The clinical dilemma is the escape from gene addiction, which is mediated, in part, by phenotypic plasticity as exemplified by epithelial-to-mesenchymal transition and mesenchymal-to-epithelial transition. Finally, cancer stem cells are now recognized as the basis for minimal residual disease and malignant progression over time. These themes cooperate in breast cancer, as induction of epithelial-to-mesenchymal transition enhances self-renewal and expression of cancer stem cells, which are believed to facilitate tumor resistance. BioMed Central 2011 2011-10-25 /pmc/articles/PMC3262190/ /pubmed/22067349 http://dx.doi.org/10.1186/bcr2887 Text en Copyright ©2011 BioMed Central Ltd |
spellingShingle | Review Cardiff, Robert D Couto, Suzana Bolon, Brad Three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells |
title | Three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells |
title_full | Three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells |
title_fullStr | Three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells |
title_full_unstemmed | Three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells |
title_short | Three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells |
title_sort | three interrelated themes in current breast cancer research: gene addiction, phenotypic plasticity, and cancer stem cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262190/ https://www.ncbi.nlm.nih.gov/pubmed/22067349 http://dx.doi.org/10.1186/bcr2887 |
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