Peak M J, Pfaff M, Peraino C
Biological, Environmental, and Medical Research Division, Argonne National Laboratory, IL 60439-4833.
Br J Cancer. 1989 Aug;60(2):220-2. doi: 10.1038/bjc.1989.255.
Administration of the photoactivable compound chlorpromazine (CPZ) to SKH-1 hairless mice via their drinking water (CPZ, 0.01%) significantly reduced the rates of accumulation and yields of squamous cell carcinomas induced by long-term repeated exposures of these animals to solar UV radiation. This protective effect of CPZ was partially reversed in mice given a single injection of ethyl nitrosourea at birth. In in vitro studies, the presence of CPZ (0.2 mM) in mammalian cell cultures enhanced the yield of DNA single-strand breaks induced in the cells by exposure to monochromatic UVA radiation at 334 nm. Collectively, the results suggest that CPZ may exert antineoplastic effects against UV-induced skin tumours by the induction of DNA damage.
通过饮用水(0.01%氯丙嗪,CPZ)给SKH-1无毛小鼠施用可光活化化合物氯丙嗪,显著降低了这些动物长期反复暴露于太阳紫外线辐射所诱导的鳞状细胞癌的累积率和发生率。CPZ的这种保护作用在出生时单次注射乙基亚硝基脲的小鼠中部分被逆转。在体外研究中,哺乳动物细胞培养物中存在CPZ(0.2 mM)可提高细胞暴露于334 nm单色UVA辐射时诱导的DNA单链断裂的发生率。总体而言,结果表明CPZ可能通过诱导DNA损伤对紫外线诱导的皮肤肿瘤发挥抗肿瘤作用。