Genotoxic Anti-Cancer Agents and Their Relationship to DNA Damage, Mitosis, and Checkpoint Adaptation in Proliferating Cancer Cells

When a human cell detects damaged DNA, it initiates the DNA damage response (DDR) that permits it to repair the damage and avoid transmitting it to daughter cells. Despite this response, changes to the genome occur and some cells, such as proliferating cancer cells, are prone to genome instability....

Full description

Bibliographic Details
Main Authors: Lucy H. Swift, Roy M. Golsteyn
Format: Article
Language:English
Published: MDPI AG 2014-02-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/15/3/3403
id doaj-396292cc227347c9bbeedd85cab85dd2
record_format Article
spelling doaj-396292cc227347c9bbeedd85cab85dd22020-11-24T21:13:34ZengMDPI AGInternational Journal of Molecular Sciences1422-00672014-02-011533403343110.3390/ijms15033403ijms15033403Genotoxic Anti-Cancer Agents and Their Relationship to DNA Damage, Mitosis, and Checkpoint Adaptation in Proliferating Cancer CellsLucy H. Swift0Roy M. Golsteyn1Cancer Cell Laboratory, Department of Biological Sciences, 4401 University Dr, University of Lethbridge, Lethbridge, AB T1K 3M4, CanadaCancer Cell Laboratory, Department of Biological Sciences, 4401 University Dr, University of Lethbridge, Lethbridge, AB T1K 3M4, CanadaWhen a human cell detects damaged DNA, it initiates the DNA damage response (DDR) that permits it to repair the damage and avoid transmitting it to daughter cells. Despite this response, changes to the genome occur and some cells, such as proliferating cancer cells, are prone to genome instability. The cellular processes that lead to genomic changes after a genotoxic event are not well understood. Our research focuses on the relationship between genotoxic cancer drugs and checkpoint adaptation, which is the process of mitosis with damaged DNA. We examine the types of DNA damage induced by widely used cancer drugs and describe their effects upon proliferating cancer cells. There is evidence that cell death caused by genotoxic cancer drugs in some cases includes exiting a DNA damage cell cycle arrest and entry into mitosis. Furthermore, some cells are able to survive this process at a time when the genome is most susceptible to change or rearrangement. Checkpoint adaptation is poorly characterised in human cells; we predict that increasing our understanding of this pathway may help to understand genomic instability in cancer cells and provide insight into methods to improve the efficacy of current cancer therapies.http://www.mdpi.com/1422-0067/15/3/3403Cdk1mitosistissue cultureanti-cancer drugsDNA repair
collection DOAJ
language English
format Article
sources DOAJ
author Lucy H. Swift
Roy M. Golsteyn
spellingShingle Lucy H. Swift
Roy M. Golsteyn
Genotoxic Anti-Cancer Agents and Their Relationship to DNA Damage, Mitosis, and Checkpoint Adaptation in Proliferating Cancer Cells
International Journal of Molecular Sciences
Cdk1
mitosis
tissue culture
anti-cancer drugs
DNA repair
author_facet Lucy H. Swift
Roy M. Golsteyn
author_sort Lucy H. Swift
title Genotoxic Anti-Cancer Agents and Their Relationship to DNA Damage, Mitosis, and Checkpoint Adaptation in Proliferating Cancer Cells
title_short Genotoxic Anti-Cancer Agents and Their Relationship to DNA Damage, Mitosis, and Checkpoint Adaptation in Proliferating Cancer Cells
title_full Genotoxic Anti-Cancer Agents and Their Relationship to DNA Damage, Mitosis, and Checkpoint Adaptation in Proliferating Cancer Cells
title_fullStr Genotoxic Anti-Cancer Agents and Their Relationship to DNA Damage, Mitosis, and Checkpoint Adaptation in Proliferating Cancer Cells
title_full_unstemmed Genotoxic Anti-Cancer Agents and Their Relationship to DNA Damage, Mitosis, and Checkpoint Adaptation in Proliferating Cancer Cells
title_sort genotoxic anti-cancer agents and their relationship to dna damage, mitosis, and checkpoint adaptation in proliferating cancer cells
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2014-02-01
description When a human cell detects damaged DNA, it initiates the DNA damage response (DDR) that permits it to repair the damage and avoid transmitting it to daughter cells. Despite this response, changes to the genome occur and some cells, such as proliferating cancer cells, are prone to genome instability. The cellular processes that lead to genomic changes after a genotoxic event are not well understood. Our research focuses on the relationship between genotoxic cancer drugs and checkpoint adaptation, which is the process of mitosis with damaged DNA. We examine the types of DNA damage induced by widely used cancer drugs and describe their effects upon proliferating cancer cells. There is evidence that cell death caused by genotoxic cancer drugs in some cases includes exiting a DNA damage cell cycle arrest and entry into mitosis. Furthermore, some cells are able to survive this process at a time when the genome is most susceptible to change or rearrangement. Checkpoint adaptation is poorly characterised in human cells; we predict that increasing our understanding of this pathway may help to understand genomic instability in cancer cells and provide insight into methods to improve the efficacy of current cancer therapies.
topic Cdk1
mitosis
tissue culture
anti-cancer drugs
DNA repair
url http://www.mdpi.com/1422-0067/15/3/3403
work_keys_str_mv AT lucyhswift genotoxicanticanceragentsandtheirrelationshiptodnadamagemitosisandcheckpointadaptationinproliferatingcancercells
AT roymgolsteyn genotoxicanticanceragentsandtheirrelationshiptodnadamagemitosisandcheckpointadaptationinproliferatingcancercells
_version_ 1716748820538195968