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紫外线照射的全身效应预防小鼠化学诱导的两阶段皮肤癌发生。

Prevention of chemically induced two-stage skin carcinogenesis in mice by systemic effects of ultraviolet irradiation.

作者信息

Gensler H L

机构信息

Department of Radiation Oncology, University of Arizona College of Medicine, Tucson 85724.

出版信息

Carcinogenesis. 1988 May;9(5):767-9. doi: 10.1093/carcin/9.5.767.

Abstract

Systemic effects of UVB irradiation (280 to 320 nm) have been shown to enhance subsequent carcinogenesis induced by UV irradiation or by high doses of benzo[a]pyrene. In the present study, we asked whether the systemic effects of UVB irradiation would influence subsequent chemical tumorigenesis induced by the initiation-promotion protocol. A group of B6D2F1/J mice were irradiated dorsally with five 30-min treatments per week for 11.5 weeks. The irradiation source was a bank of six unfiltered Westinghouse FS40 sun lamps. One week later, irradiated and unirradiated mice were initiated ventrally with 100 micrograms of 7,12-dimethylbenz[a]anthracene. Four days later, ventral 12-O-tetradecanoylphorbol-13-acetate treatments were begun. After 20 weeks of promotion, there were 75% fewer tumors per mouse in the irradiated mice than in unirradiated mice. Thus, systemic effects of UVB irradiation resulted in inhibition of chemical carcinogenesis induced with an initiation-promotion protocol.

摘要

紫外线B(UVB)照射(280至320纳米)的全身效应已被证明会增强随后由紫外线照射或高剂量苯并[a]芘诱导的致癌作用。在本研究中,我们探究了UVB照射的全身效应是否会影响随后通过启动-促进方案诱导的化学致癌作用。一组B6D2F1/J小鼠每周接受5次每次30分钟的背部照射,持续11.5周。照射源是一排六个未过滤的西屋FS40日光灯。一周后,对照射过和未照射过的小鼠进行腹部注射100微克的7,12-二甲基苯并[a]蒽以启动致癌过程。四天后,开始进行腹部12-O-十四酰佛波醇-13-乙酸酯处理。经过20周的促进阶段后,照射组小鼠每只身上的肿瘤数量比未照射组小鼠少75%。因此,UVB照射的全身效应导致了对通过启动-促进方案诱导的化学致癌作用的抑制。

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