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PMID: 10924858 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Oxidative stress and cell cycle checkpoint function.

Free radical biology & medicine ·Vol. 28 ·No. 9 ·2000-05-01 ·Pages 1387-404

Shackelford RE, Kaufmann WK, Paules RS

Abstract

Oxidative stress and the damage that results from it have been implicated in a wide number of disease processes including atherosclerosis, autoimmune disorders, neuronal degeneration, and cancer. Reactive oxygen species (ROS) are ubiquitous and occur naturally in all aerobic species, coming from both exogenous and endogenous sources. ROS are quite reactive and readily damage biological molecules, including DNA. While the damaging effects of ROS on DNA have been intensively studied, the effects of oxidative damage on cell cycle checkpoint function have not. Here will we review several biologically important ROS and their sources, the cell cycle, checkpoints, and current knowledge about the effects of ROS on initiating checkpoint responses.

MeSH Terms
Aerobiosis Animals Apoptosis/physiology Cell Cycle/physiology Cell Cycle Proteins/physiology Cells/radiation effects Cyclins/physiology DNA Damage DNA Repair DNA Replication Electron Transport Gene Expression Regulation/physiology Humans Hydrogen Peroxide/metabolism Hydroxyl Radical/metabolism Inflammation/metabolism Models, Biological Nitric Oxide/metabolism Oxidation-Reduction Oxidative Stress/physiology Reactive Oxygen Species Superoxides/metabolism
Chemicals
Cell Cycle Proteins Cyclins Reactive Oxygen Species Superoxides Nitric Oxide Hydroxyl Radical Hydrogen Peroxide
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Shackelford R E
Growth Control and Cancer Group, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Kaufmann W K
Paules R S
Article Info
Journal
Free radical biology & medicine
Abbr.
Free Radic Biol Med
ISSN
0891-5849
Published
2000-05-01
Pages
1387-404
Language
English
Region
United States
NLM ID
8709159
Subset
IM
Grants
NCI NIH HHS · CA42765 · United States
NCI NIH HHS · CA81343 · United States
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