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PMID: 7705290 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Potential molecular mechanisms of oxidant-induced carcinogenesis.

Environmental health perspectives ·Vol. 102 Suppl 10 ·1994-12-00 ·Pages 155-7

Jackson JH

Abstract

Chronic exposure to oxidants is associated with an increased incidence of malignancy; however, the mechanism(s) by which oxidants contribute to carcinogenesis is unknown. Since oncogene activation plays an important role in carcinogenesis, we hypothesized that hydroxyl radical-induced DNA damage might contribute to carcinogenesis by causing oncogene activation. The studies reported herein demonstrate that hydroxyl radical-induced DNA damage can activate the K-ras 4B and C-Raf-l oncogenes by causing point mutations and deletions, respectively. In addition, our results indicate that a) hydroxyl radical-induced DNA damage causes selective base substitutions; b) the four DNA bases have different susceptibilities to hydroxyl radical-induced mutations; and c) hydroxyl radical-induced mutations are not randomly distributed among oncogene codons. Our studies suggest that oncogene activation could be one potential mechanism by which oxidants contribute to carcinogenesis.

MeSH Terms
Carcinogens/pharmacology DNA Damage Gene Expression Regulation Humans Hydroxyl Radical/pharmacology Oncogenes
Chemicals
Carcinogens Hydroxyl Radical
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Jackson J H
Department of Immunology, Scripps Research Institute, La Jolla, California 92037.
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24 references, click to expand
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Article Info
Journal
Environmental health perspectives
Abbr.
Environ Health Perspect
ISSN
0091-6765
Published
1994-12-00
Pages
155-7
Language
English
Region
United States
NLM ID
0330411
PMCID
PMC1567006
Subset
IM
Grants
NCI NIH HHS · CA-54298 · United States
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