Allelic losses in mouse skin tumors induced by γ-irradiation of p53 heterozygotes

被引:9
作者
Miyazawa, T
Sato, H
Hatakeyama, K
Kitagawa, T
Kominami, R
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Dept Gene Regulat, Niigata 9518510, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Dept Regenerat & Transplantat Med, Niigata 9518510, Japan
[3] Japanese Fdn Canc Res, Inst Canc, Tokyo 1700012, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 2002年 / 93卷 / 09期
关键词
gamma-ray; mouse skin tumors; LOH; tumor suppressor gene; genomic instability;
D O I
10.1111/j.1349-7006.2002.tb02475.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Skin tumors were induced by gamma-irradiation in F, mice between C3H/He or BALB/c and MSM carrying a p53-deficient allele. The incidence was 39.1% (34/87) in p53(KO/+) mice of the C3H/MSM genetic background and 14.3% (19/133) in those of the BALB/MSM background. Interestingly, most of the tumors (82 %) lost the wild-type p53 allele and no skin tumor was found in p53(+/+) F-1 mice. This suggests a requirement of p53 loss for the skin cancer development. Genome scan localized a chromosomal locus showing frequent allelic losses near D12MiO, which may harbor a tumor suppressor gene. In addition, 23 loci distributed on 13 chromosomes exhibited allelic losses at frequencies of more than 20%. The genome-wide occurrence of allelic losses suggests that genomic instability of the skin tumors may be implicated in radiation-induced carcinogenesis. The present study is the first to report a mouse model system useful for the analysis of radiation induction of skin cancer in man.
引用
收藏
页码:994 / 999
页数:6
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