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Translesion Synthesis Polymerases in the Prevention and Promotion of Carcinogenesis

A critical step in the transformation of cells to the malignant state of cancer is the induction of mutations in the DNA of cells damaged by genotoxic agents. Translesion DNA synthesis (TLS) is the process by which cells copy DNA containing unrepaired damage that blocks progression of the replicatio...

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Detalles Bibliográficos
Autores principales: Stallons, L. Jay, McGregor, W. Glenn
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945679/
https://www.ncbi.nlm.nih.gov/pubmed/20936171
http://dx.doi.org/10.4061/2010/643857
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author Stallons, L. Jay
McGregor, W. Glenn
author_facet Stallons, L. Jay
McGregor, W. Glenn
author_sort Stallons, L. Jay
collection PubMed
description A critical step in the transformation of cells to the malignant state of cancer is the induction of mutations in the DNA of cells damaged by genotoxic agents. Translesion DNA synthesis (TLS) is the process by which cells copy DNA containing unrepaired damage that blocks progression of the replication fork. The DNA polymerases that catalyze TLS in mammals have been the topic of intense investigation over the last decade. DNA polymerase η (Pol η) is best understood and is active in error-free bypass of UV-induced DNA damage. The other TLS polymerases (Pol ι, Pol κ, REV1, and Pol ζ) have been studied extensively in vitro, but their in vivo role is only now being investigated using knockout mouse models of carcinogenesis. This paper will focus on the studies of mice and humans with altered expression of TLS polymerases and the effects on cancer induced by environmental agents.
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spelling pubmed-29456792010-10-08 Translesion Synthesis Polymerases in the Prevention and Promotion of Carcinogenesis Stallons, L. Jay McGregor, W. Glenn J Nucleic Acids Review Article A critical step in the transformation of cells to the malignant state of cancer is the induction of mutations in the DNA of cells damaged by genotoxic agents. Translesion DNA synthesis (TLS) is the process by which cells copy DNA containing unrepaired damage that blocks progression of the replication fork. The DNA polymerases that catalyze TLS in mammals have been the topic of intense investigation over the last decade. DNA polymerase η (Pol η) is best understood and is active in error-free bypass of UV-induced DNA damage. The other TLS polymerases (Pol ι, Pol κ, REV1, and Pol ζ) have been studied extensively in vitro, but their in vivo role is only now being investigated using knockout mouse models of carcinogenesis. This paper will focus on the studies of mice and humans with altered expression of TLS polymerases and the effects on cancer induced by environmental agents. SAGE-Hindawi Access to Research 2010-09-22 /pmc/articles/PMC2945679/ /pubmed/20936171 http://dx.doi.org/10.4061/2010/643857 Text en Copyright © 2010 L. J. Stallons and W. G. McGregor. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Stallons, L. Jay
McGregor, W. Glenn
Translesion Synthesis Polymerases in the Prevention and Promotion of Carcinogenesis
title Translesion Synthesis Polymerases in the Prevention and Promotion of Carcinogenesis
title_full Translesion Synthesis Polymerases in the Prevention and Promotion of Carcinogenesis
title_fullStr Translesion Synthesis Polymerases in the Prevention and Promotion of Carcinogenesis
title_full_unstemmed Translesion Synthesis Polymerases in the Prevention and Promotion of Carcinogenesis
title_short Translesion Synthesis Polymerases in the Prevention and Promotion of Carcinogenesis
title_sort translesion synthesis polymerases in the prevention and promotion of carcinogenesis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945679/
https://www.ncbi.nlm.nih.gov/pubmed/20936171
http://dx.doi.org/10.4061/2010/643857
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