Miyazawa Tomonori, Sato Hiroki, Hatakeyama Katsuyoshi, Kitagawa Tomoyuki, Kominami Ryo
Department of Gene Regulation, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
Jpn J Cancer Res. 2002 Sep;93(9):994-9. doi: 10.1111/j.1349-7006.2002.tb02475.x.
Skin tumors were induced by gamma-irradiation in F(1) 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 D12Mit2, 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.
通过γ射线照射,在携带p53缺陷等位基因的C3H/He或BALB/c与MSM之间的F(1)代小鼠中诱发皮肤肿瘤。在C3H/MSM遗传背景的p53(KO/+)小鼠中,发病率为39.1%(34/87),在BALB/MSM背景的小鼠中为14.3%(19/133)。有趣的是,大多数肿瘤(82%)丢失了野生型p53等位基因,并且在p53(+ / +) F(1)代小鼠中未发现皮肤肿瘤。这表明p53缺失是皮肤癌发生所必需的。基因组扫描在D12Mit2附近定位了一个显示频繁等位基因缺失的染色体位点,该位点可能含有一个肿瘤抑制基因。此外,分布在13条染色体上的23个位点表现出频率超过20%的等位基因缺失。全基因组范围内等位基因缺失的发生表明皮肤肿瘤的基因组不稳定性可能与辐射诱导的致癌作用有关。本研究首次报道了一个可用于分析人类皮肤癌辐射诱导的小鼠模型系统。