Cited by 291DNA Repair MechanismsCarcinogens and Genotoxicity AssessmentGenetic factors in colorectal cancer

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Deficiencies in Mouse Myh and Ogg1 Result in Tumor Predisposition and G to T Mutations in Codon 12 of the K-Ras Oncogene in Lung Tumors

Xie, Yali, Yang, Hanjing, Cunanan, Cristina, Okamoto, Kimberly, Shibata, Darryl, Pan, Janet, Barnes, Deborah E., Lindahl, Tomas, McIlhatton, Michael, Fishel, Richard, Miller, Jeffrey H.·2004·Cancer Research

DOI 10.1158/0008-5472.can-03-3834

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Abstract

Oxidative DNA damage is unavoidably and continuously generated by oxidant byproducts of normal cellular metabolism. The DNA damage repair genes, mutY and mutM, prevent G to T mutations caused by reactive oxygen species in Escherichia coli, but it has remained debatable whether deficiencies in their mammalian counterparts, Myh and Ogg1, are directly involved in tumorigenesis. Here, we demonstrate that deficiencies in Myh and Ogg1 predispose 65.7% of mice to tumors, predominantly lung and ovarian tumors, and lymphomas. Remarkably, subsequent analyses identified G to T mutations in 75% of the lung tumors at an activating hot spot, codon 12, of the K-ras oncogene, but none in their adjacent normal tissues. Moreover, malignant lung tumors were increased with combined heterozygosity of Msh2, a mismatch repair gene involved in oxidative DNA damage repair as well. Thus, oxidative DNA damage appears to play a causal role in tumorigenesis, and codon 12 of K-ras is likely to be an important downstream target in lung tumorigenesis. The multiple oxidative repair genes are required to prevent mutagenesis and tumor formation. The mice described here provide a valuable model for studying the mechanisms of oxidative DNA damage in tumorigenesis and investigating preventive or therapeutic approaches.

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Deciphering the role of xeroderma pigmentosum C (XPC) protein in base excision repair (BER) and oxidative stress
Fayyad, N. (2021) · theses.fr (ABES) · doi:10.70675/180d97efzbb9cz4e9fzaa97z25f2a7d87dc0

Authors: Xie, Y., Yang, H., Cunanan, C., Okamoto, K., Shibata, D., Pan, J., Barnes, D. E., Lindahl, T., McIlhatton, M., Fishel, R., & Miller, J. H.
Affiliations: University of California, Los Angeles (US)
University of Southern California (US)
Cancer Research UK (GB)
Thomas Jefferson University (US)
ORCID: Yang, Hanjing
Shibata, Darryl
Lindahl, Tomas
McIlhatton, Michael
Fishel, Richard
Miller, Jeffrey H.
Venue: Cancer Research
Publisher: American Association for Cancer Research (AACR)
Published: 2004-05-01
Volume: 64
Issue: 9
Pages: 3096-3102
ISSN: 0008-5472 (ISSN-L)
1538-7445
DOI: 10.1158/0008-5472.can-03-3834
OpenAlex: W2137854060
Cited by: 291
References: 38
Citations by year: 2026: 2 · 2025: 4 · 2024: 7 · 2023: 4 · 2022: 8 · 2021: 15 · 2020: 10 · 2019: 16 · 2018: 11 · 2017: 10 · 2016: 11 · 2015: 11 · 2014: 14 · 2013: 15 · 2012: 17
FWCI: 7.22
Type: journal article
Language: en
Open access: closed
Locations: Cancer Research (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (5r01ca085952-04)
National Cancer Institute (CA 85952)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
Keywords: MUTYH, OGG1, oxidative DNA damage, lung cancer, cancer susceptibility, MutY, formamidopyrimidine-DNA glycosylase, MSH2, DNA mismatch repair, oxidative DNA damage repair, mutagenesis, lymphoma, ovarian neoplasms, reactive oxygen species, mouse model
MeSH terms: Animals, Codon, DNA Damage, DNA-Binding Proteins, Female, Humans, Lung Neoplasms, Lymphoma, Male, Mice, Inbred C57BL, Ovarian Neoplasms, Oxidation-Reduction, Proto-Oncogene Proteins, Genes, ras, Point Mutation, Mice, Knockout, Genetic Predisposition to Disease, DNA Glycosylases, Mice, MutS Homolog 2 Protein

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Deficiencies in Mouse Myh and Ogg1 Result in Tumor Predisposition and G to T Mutations in Codon 12 of the K-Ras Oncogene in Lung Tumors

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