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Chlorpromazine reduces UV-induced squamous cell carcinogenesis in hairless mice and enhances UV-induced DNA damage in cultured cells.氯丙嗪可减少无毛小鼠紫外线诱导的鳞状细胞癌发生,并增强培养细胞中紫外线诱导的DNA损伤。
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Skin tumor development after UV irradiation and photodynamic therapy is unaffected by short-term pretreatment with 5-fluorouracil, imiquimod and calcipotriol. An experimental hairless mouse study.紫外线照射和光动力治疗后皮肤肿瘤的发生不受5-氟尿嘧啶、咪喹莫特和卡泊三醇短期预处理的影响。一项无毛小鼠实验研究。
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The phenomenon of phototoxicity and long-term risks of commonly prescribed and structurally diverse drugs.常用且结构多样药物的光毒性现象及长期风险。
J Photochem Photobiol. 2024 Feb;19. doi: 10.1016/j.jpap.2023.100221. Epub 2023 Dec 5.

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Inhibitory action of chlorpromazine, dibucaine, and other phospholipid-interacting drugs on calcium-activated, phospholipid-dependent protein kinase.氯丙嗪、丁卡因及其他与磷脂相互作用药物对钙激活的、磷脂依赖性蛋白激酶的抑制作用。
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Do tumor promoters affect DNA after all?
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氯丙嗪可减少无毛小鼠紫外线诱导的鳞状细胞癌发生,并增强培养细胞中紫外线诱导的DNA损伤。

Chlorpromazine reduces UV-induced squamous cell carcinogenesis in hairless mice and enhances UV-induced DNA damage in cultured cells.

作者信息

Peak M J, Pfaff M, Peraino C

机构信息

Biological, Environmental, and Medical Research Division, Argonne National Laboratory, IL 60439-4833.

出版信息

Br J Cancer. 1989 Aug;60(2):220-2. doi: 10.1038/bjc.1989.255.

DOI:10.1038/bjc.1989.255
PMID:2765369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2247052/
Abstract

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.

摘要

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。