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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...

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Detalles Bibliográficos
Autores principales: Cardiff, Robert D, Couto, Suzana, Bolon, Brad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
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.
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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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