Xeroderma pigmentosum group A gene action as a protection factor against 4-nitroquinoline 1-oxide-induced tongue carcinogenesis

被引:32
作者
Ide, F
Oda, H
Nakatsuru, Y
Kusama, K
Sakashita, H
Tanaka, K
Ishikawa, T [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
[2] Meikai Univ, Sch Dent, Dept Oral & Maxillofacial Surg 2, Sakado, Saitama 3500283, Japan
[3] Osaka Univ, Inst Mol & Cellular Biol, Div Cellular Genet, Suita, Osaka 5650871, Japan
[4] Univ Tokyo, Fac Evaluat & Res, Natl Inst Acad Degrees, Chiyoda Ku, Tokyo 1010003, Japan
关键词
D O I
10.1093/carcin/22.4.567
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To test the hypothesis that nucleotide excision repair (NER) plays a protective role in chemical carcinogenesis in internal organs, xeroderma pigmentosum group A gene-deficient (XPAJ(-/-)) mice, heterozygous (XPA(+/-)) and wild-type (XPA(+/+)) mice were orally administered 0.001% 4-nitroquinoline 1-oxide (4NQO) in their drinking water and compared. After 50 weeks of 4NQO exposure, tongue squamous cell carcinomas (SCCs) occurred in XPA(-/-) mice only, no tumors being observed in XPA(+/-) and XPA(+/+) animals. Of the XPA(-/-) mice 86% had tumors and 100% demonstrated multiple foci of dysplastic epithelium in the tongue. Accumulation of p53 protein was immunohistochemically detected in 56% of the SCCs, Mutational analysis of the p53 gene (exons 4-10) in carcinoma DNA revealed missense mutations in exons 5 and 9 in four of 20 samples. Our results clearly demonstrate that the NER gene XPA acts as a defensive factor against 4NQO-induced tongue carcinogenesis in vivo.
引用
收藏
页码:567 / 572
页数:6
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