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Carcinogenesis Advance Access originally published online on April 8, 2004
Carcinogenesis 2004 25(9):1689-1694; doi:10.1093/carcin/bgh166
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Carcinogenesis vol.25 no.9 © Oxford University Press 2004; all rights reserved.

ARTICLE

Differential ability of polymorphic OGG1 proteins to suppress mutagenesis induced by 8-hydroxyguanine in human cell in vivo

Arito Yamane1,4, Takashi Kohno1, Kohei Ito1, Noriaki Sunaga1, Kazunori Aoki3, Kimio Yoshimura2, Hirokazu Murakami5, Yoshihisa Nojima4 and Jun Yokota1,6

1 Biology Division, 2 Genetics Division and 3 Section for Studies on Host-immune Response, National Cancer Center Research Institute, 1-1 Tsukiji 5-chome, Chuo-ku, Tokyo 104-0045, 4 Department of Medicine and Clinical Science and 5 School of Health Sciences, Faculty of Medicine, School of Medicine, Gunma University, 39-15 Showa-machi 3-chome, Maebashi 371-8511, Japan

6 To whom correspondence should be addressed Email: jyokota{at}gan2.ncc.go.jp

OGG1 protein has an ability to suppress mutagenesis induced by 8-hydroxyguanine (8OHG), an oxidatively damaged promutagenic base. Here, the mutation suppressive ability was compared between two common polymorphic OGG1 proteins, OGG1-Ser326 and OGG1-Cys326, using a supF forward mutation assay employing an 8OHG-containing plasmid. Polymorphic OGG1 proteins were exogenously expressed by adenoviral transduction in H1299 human lung cancer cells, in which endogenous OGG1 protein was undetectable by western blot analysis. Mutations by 8OHG were more efficiently suppressed in OGG1-Ser326 transduced cells than OGG1-Cys326 transduced cells. The results indicated that OGG1-Cys326 has a lower ability to prevent mutagenesis by 8OHG than OGG1-Ser326 in vivo in human cells; supporting the results of recent association studies that OGG1-Cys326 is a risk allele for several types of human cancers.


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