Sato H, Suzuki J S, Tanaka M, Ogiso M, Tohyama C, Kobayashi S
Kyoritsu College of Pharmacy, Tokyo, Japan.
Photochem Photobiol. 1997 May;65(5):908-14. doi: 10.1111/j.1751-1097.1997.tb01942.x.
We investigated the expressions of c-Ha-ras, c-jun, c-fos, c-myc genes and p53 protein in the development of skin tumors induced by chronic exposure to UVB without a photosensitizer using hairless mice. When mice were exposed to UVB at a dose of 2 kJ/m2 three times a week, increased c-Ha-ras and c-myc transcripts were detected after only 5 weeks of exposure, while no tumor appeared on the exposed skin. The increase in gene expression continued until 25 weeks, when tumors, identified pathologically as mainly squamous cell carcinomas (SCC), developed in the dorsal skin. In these SCC, overexpression of c-fos mRNA was also observed along with the increases in c-Ha-ras and c-myc. A single dose of UVB (2 kJ/m2) applied to the backs of hairless mice transiently induced overexpression of the early event genes c-fos, c-jun and c-myc, but not c-Ha-ras, in the exposed area of skin. Accumulation of p53 protein was determined by Western blotting analysis or immunohistochemistry using monoclonal antibodies PAb 240 or 246, which recognize mutant or wild type, respectively. In the SCC, a mutant p53 protein accumulated in the cytoplasm and nucleus. After single-dose irradiation, the increased wild-type p53 protein was observed in the nuclei of epidermal cells. The present results suggest that overexpression of the c-fos, c-myc and c-Ha-ras genes, and the mutational changes in p53 protein might be associated with skin photocarcinogenesis. Moreover, overexpression of the c-Ha-ras and c-myc genes might be an early event in the development of UVB-induced skin tumors in mice.
我们使用无毛小鼠,研究了在无光敏剂的情况下长期暴露于UVB诱导皮肤肿瘤发生过程中c-Ha-ras、c-jun、c-fos、c-myc基因和p53蛋白的表达情况。当小鼠每周接受3次剂量为2 kJ/m2的UVB照射时,仅在照射5周后就检测到c-Ha-ras和c-myc转录本增加,而暴露的皮肤上未出现肿瘤。基因表达的增加一直持续到25周,此时背部皮肤出现了经病理鉴定主要为鳞状细胞癌(SCC)的肿瘤。在这些SCC中,除了c-Ha-ras和c-myc增加外,还观察到c-fos mRNA的过表达。单次剂量的UVB(2 kJ/m2)照射无毛小鼠背部,可在皮肤暴露区域短暂诱导早期事件基因c-fos、c-jun和c-myc的过表达,但不会诱导c-Ha-ras的过表达。使用分别识别突变型或野生型的单克隆抗体PAb 240或246,通过蛋白质印迹分析或免疫组织化学法测定p53蛋白的积累情况。在SCC中,突变型p53蛋白在细胞质和细胞核中积累。单次剂量照射后,在表皮细胞核中观察到野生型p53蛋白增加。目前的结果表明,c-fos、c-myc和c-Ha-ras基因的过表达以及p53蛋白的突变变化可能与皮肤光致癌作用有关。此外,c-Ha-ras和c-myc基因的过表达可能是小鼠UVB诱导皮肤肿瘤发生过程中的早期事件。