8-Oxoguanine Formation Induced by Chronic UVB Exposure Makes <i>Ogg1</i> Knockout Mice Susceptible to Skin Carcinogenesis

Cancer Research - Tập 65 Số 14 - Trang 6006-6010 - 2005
Makoto Kunisada1, Kunihiko Sakumi2, Yohei Tominaga2, Arief Budiyanto1, Masato Ueda1, Masamitsu Ichihashi1, Yusaku Nakabeppu2, Chikako Nishigori1
11Division of Dermatology, Clinical Molecular Medicine, Faculty of Medicine, Kobe University Graduate School of Medicine, Kobe, Japan and
22Division of Neurofunctional Genomics, Medical Institute of Bioregulation, Kyusyu University, Fukuoka, Japan

Tóm tắt

Abstract 8-Oxoguanine is one of the oxidative DNA damages that can result in stable mutations. The Ogg1 gene encodes the repair enzyme 8-oxoguanine-DNA glycosylase, which removes the oxidized base from DNA. In this study, we investigated the role of 8-oxoguanine in skin carcinogenesis induced by UVB irradiation using Ogg1 knockout mice (C57Bl/6J background). We examined the effect of UVB irradiation on the formation of 8-oxoguanine in epidermal cells using immunostaining and found that the level of 8-oxoguanine in Ogg1 knockout mice 24 hours after UVB irradiation remained high compared with that in wild-type and heterozygous mice. To verify the effect of chronic UVB irradiation on 8-oxoguanine formations in epidermal cells, we irradiated wild-type, heterozygous, and Ogg1 knockout mice with UVB at a dose of 2.5 kJ/m2 thrice a week for 40 weeks. We found that the mean number of tumors in Ogg1 knockout mice was 3.71, which was significantly more than in wild-type and heterozygous mice, being 1.71 and 2.28, respectively. The rate of developing malignant tumors in Ogg1 knockout mice was also significantly higher (88.5%; squamous cell carcinomas, 73.1%; sarcomas, 15.4%) than in wild-type mice (50.0%; squamous cell carcinomas, 41.7%; sarcomas, 8.3%). Moreover, the age of onset of developing skin tumors in Ogg1 knockout mice was earlier than in the other types of mice. These results clearly indicate that oxidative DNA damage induced by sunlight plays an important role in the development of skin cancers.

Từ khóa


Tài liệu tham khảo

Kasai H, Chung MH, Jones DS, et al. 8-Hydroxyguanine, a DNA adduct formed by oxygen radicals: its implication on oxygen radical-involved mutagenesis/carcinogenesis. J Toxicol Sci 1991; 16: 95–105.

Maki H, Sekiguchi M. MutT protein specifically hydrolyses a potent mutagenic substrate for DNA synthesis. Nature 1992; 355: 273–5.

Aburatani H, Hippo Y, Ishida T, et al. Cloning and characterization of mammalian 8-hydroxyguanine-specific DNA glycosylase/apurinic, apyrimidinic lyase, a functional mutM homologue. Cancer Res 1997; 57: 2151–6.

Kraemer KH. Sunlight and skin cancer: another link revealed. Proc Natl Acad Sci U S A 1997; 94: 11–4.

Drobetsky EA, Grosovsky AJ, Glickman BW. The specificity of UV-induced mutations at an endogenous locus in mammalian cells. Proc Natl Acad Sci U S A 1987; 84: 9103–7.

Nishigori C, Hattori Y, Toyokuni S. Role of reactive oxygen species in skin carcinogenesis. Antioxid Redox Signal 2004; 6: 561–70.

Yamamoto F, Nishimura S, Kasai H. Photosensitized formation of 8-hydroxydeoxyguanosine in cellular DNA by riboflavin. Biochem Biophys Res Commun 1992; 187: 809–13.

Hattori Y, Nishigori C, Tanaka T, et al. 8-Hydroxy-2′-deoxyguanosine is increased in epidermal cells of hairless mice after chronic ultraviolet B exposure. J Invest Dermatol 1996; 107: 733–7.

Sakumi K, Tominaga Y, Furuichi M, et al. Ogg1 knockout-associated lung tumorigenesis and its suppression by Mth1 gene disruption. Cancer Res 2003; 63: 902–5.

Hardie LJ, Briggs JA, Davidson LA, et al. The effect of hOGG1 and glutathione peroxidase I genotypes and 3p chromosomal loss on 8-hydroxydeoxyguanosine levels in lung cancer. Carcinogenesis 2000; 21: 167–72.

Xu J, Zheng SL, Turner A, et al. Associations between hOGG1 sequence variants and prostate cancer susceptibility. Cancer Res 2002; 62: 2253–7.

Hattori-Nakakuki Y, Nishigori C, Okamoto K, Imamura S, Hiai H, Toyokuni S. Formation of 8-hydroxy-2′-deoxyguanosine in epidermis of hairless mice exposed to near-UV. Biochem Biophys Res Commun 1994; 201: 1132–9.

Nishigori C, Wang S, Miyakoshi J, et al. Mutations in ras genes in cells cultured from mouse skin tumors induced by ultraviolet irradiation. Proc Natl Acad Sci U S A 1994; 91: 7189–93.

Basset-Seguin N, Moles JP, Mils V, Dereure O, Guilhou JJ. TP53 tumor suppressor gene and skin carcinogenesis. J Invest Dermatol 1994; 103: 102–6S.

Abbott PJ. Strain-specific tumorigenesis in mouse skin induced by the carcinogen, 15,16-dihydro-11-methylcyclopenta[a]phenanthren-17-one, and its relation to DNA adduct formation and persistence. Cancer Res 1983; 43: 2261–6.

Arai T, Kelly VP, Komoro K, Minowa O, Noda T, Nishimura S. Cell proliferation in liver of Mmh/Ogg1-deficient mice enhances mutation frequency because of the presence of 8-hydroxyguanine in DNA. Cancer Res 2003; 63: 4287–92.

Morrison WL, Jerdan MS, Hoover TL, Farmer ER. UV radiation-induced tumors in haired mice: identification as squamous cell carcinomas. J Natl Cancer Inst 1986; 77: 1155–62.

Guyton KZ, Kensler TW. Oxidative mechanisms in carcinogenesis. Br Med Bull 1993; 49: 523–44.

Nishigori C, Moriwaki S, Takebe H, Tanaka T, Imamura S. Gene alterations and clinical characteristics of xeroderma pigmentosum group A patients in Japan. Arch Dermatol 1994; 130: 191–7.