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(A)Symmetric Stem Cell Replication and Cancer

Most tissues in metazoans undergo continuous turnover due to cell death or epithelial shedding. Since cellular replication is associated with an inherent risk of mutagenesis, tissues are maintained by a small group of stem cells (SCs) that replicate slowly to maintain their own population and that g...

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Detalles Bibliográficos
Autores principales: Dingli, David, Traulsen, Arne, Michor, Franziska
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1828703/
https://www.ncbi.nlm.nih.gov/pubmed/17367205
http://dx.doi.org/10.1371/journal.pcbi.0030053
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author Dingli, David
Traulsen, Arne
Michor, Franziska
author_facet Dingli, David
Traulsen, Arne
Michor, Franziska
author_sort Dingli, David
collection PubMed
description Most tissues in metazoans undergo continuous turnover due to cell death or epithelial shedding. Since cellular replication is associated with an inherent risk of mutagenesis, tissues are maintained by a small group of stem cells (SCs) that replicate slowly to maintain their own population and that give rise to differentiated cells. There is increasing evidence that many tumors are also maintained by a small population of cancer stem cells that may arise by mutations from normal SCs. SC replication can be either symmetric or asymmetric. The former can lead to expansion of the SC pool. We describe a simple model to evaluate the impact of (a)symmetric SC replication on the expansion of mutant SCs and to show that mutations that increase the probability of asymmetric replication can lead to rapid mutant SC expansion in the absence of a selective fitness advantage. Mutations in several genes can lead to this process and may be at the root of the carcinogenic process.
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spelling pubmed-18287032007-04-03 (A)Symmetric Stem Cell Replication and Cancer Dingli, David Traulsen, Arne Michor, Franziska PLoS Comput Biol Research Article Most tissues in metazoans undergo continuous turnover due to cell death or epithelial shedding. Since cellular replication is associated with an inherent risk of mutagenesis, tissues are maintained by a small group of stem cells (SCs) that replicate slowly to maintain their own population and that give rise to differentiated cells. There is increasing evidence that many tumors are also maintained by a small population of cancer stem cells that may arise by mutations from normal SCs. SC replication can be either symmetric or asymmetric. The former can lead to expansion of the SC pool. We describe a simple model to evaluate the impact of (a)symmetric SC replication on the expansion of mutant SCs and to show that mutations that increase the probability of asymmetric replication can lead to rapid mutant SC expansion in the absence of a selective fitness advantage. Mutations in several genes can lead to this process and may be at the root of the carcinogenic process. Public Library of Science 2007-03 2007-03-16 /pmc/articles/PMC1828703/ /pubmed/17367205 http://dx.doi.org/10.1371/journal.pcbi.0030053 Text en © 2007 Dingli et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Dingli, David
Traulsen, Arne
Michor, Franziska
(A)Symmetric Stem Cell Replication and Cancer
title (A)Symmetric Stem Cell Replication and Cancer
title_full (A)Symmetric Stem Cell Replication and Cancer
title_fullStr (A)Symmetric Stem Cell Replication and Cancer
title_full_unstemmed (A)Symmetric Stem Cell Replication and Cancer
title_short (A)Symmetric Stem Cell Replication and Cancer
title_sort (a)symmetric stem cell replication and cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1828703/
https://www.ncbi.nlm.nih.gov/pubmed/17367205
http://dx.doi.org/10.1371/journal.pcbi.0030053
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