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Cancer Stem Cells of Differentiated B-Cell Malignancies: Models and Consequences

The concept of cancer stem cells has revolutionized our current vision of cancer development and was validated in solid tumors and cancers of the primitive hematopoietic compartment. Proof of the principle is still lacking, however, in malignancies of differentiated B-cells. We review here the curre...

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Detalles Bibliográficos
Autores principales: Gross, Emilie, Quillet-Mary, Anne, Ysebaert, Loic, Laurent, Guy, Fournie, Jean-Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757378/
https://www.ncbi.nlm.nih.gov/pubmed/24212774
http://dx.doi.org/10.3390/cancers3021566
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author Gross, Emilie
Quillet-Mary, Anne
Ysebaert, Loic
Laurent, Guy
Fournie, Jean-Jacques
author_facet Gross, Emilie
Quillet-Mary, Anne
Ysebaert, Loic
Laurent, Guy
Fournie, Jean-Jacques
author_sort Gross, Emilie
collection PubMed
description The concept of cancer stem cells has revolutionized our current vision of cancer development and was validated in solid tumors and cancers of the primitive hematopoietic compartment. Proof of the principle is still lacking, however, in malignancies of differentiated B-cells. We review here the current literature, which nevertheless suggests hierarchical organizations of the tumor clone for mostly incurable B-cell cancers such as multiple myeloma, lymphomas and B-chronic lymphocytic leukemia. We propose two models accounting for cancer stem cells in these contexts: a “top-to-bottom” clonal hierarchy from memory B-cells and a “bottom-to-top” model of clonal reprogramming. Selection pressure on the growing tumor can drive such reprogramming and increase its genetic diversity.
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spelling pubmed-37573782013-09-04 Cancer Stem Cells of Differentiated B-Cell Malignancies: Models and Consequences Gross, Emilie Quillet-Mary, Anne Ysebaert, Loic Laurent, Guy Fournie, Jean-Jacques Cancers (Basel) Review The concept of cancer stem cells has revolutionized our current vision of cancer development and was validated in solid tumors and cancers of the primitive hematopoietic compartment. Proof of the principle is still lacking, however, in malignancies of differentiated B-cells. We review here the current literature, which nevertheless suggests hierarchical organizations of the tumor clone for mostly incurable B-cell cancers such as multiple myeloma, lymphomas and B-chronic lymphocytic leukemia. We propose two models accounting for cancer stem cells in these contexts: a “top-to-bottom” clonal hierarchy from memory B-cells and a “bottom-to-top” model of clonal reprogramming. Selection pressure on the growing tumor can drive such reprogramming and increase its genetic diversity. Molecular Diversity Preservation International (MDPI) 2011-03-25 /pmc/articles/PMC3757378/ /pubmed/24212774 http://dx.doi.org/10.3390/cancers3021566 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Gross, Emilie
Quillet-Mary, Anne
Ysebaert, Loic
Laurent, Guy
Fournie, Jean-Jacques
Cancer Stem Cells of Differentiated B-Cell Malignancies: Models and Consequences
title Cancer Stem Cells of Differentiated B-Cell Malignancies: Models and Consequences
title_full Cancer Stem Cells of Differentiated B-Cell Malignancies: Models and Consequences
title_fullStr Cancer Stem Cells of Differentiated B-Cell Malignancies: Models and Consequences
title_full_unstemmed Cancer Stem Cells of Differentiated B-Cell Malignancies: Models and Consequences
title_short Cancer Stem Cells of Differentiated B-Cell Malignancies: Models and Consequences
title_sort cancer stem cells of differentiated b-cell malignancies: models and consequences
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757378/
https://www.ncbi.nlm.nih.gov/pubmed/24212774
http://dx.doi.org/10.3390/cancers3021566
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