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诱导产生的黑色素可减少小鼠黑色素瘤中的突变和细胞杀伤。

Induced melanin reduces mutations and cell killing in mouse melanoma.

作者信息

Li W, Hill H Z

机构信息

Department of Radiology, UMDNJ-New Jersey Medical School, Newark 07103, USA.

出版信息

Photochem Photobiol. 1997 Mar;65(3):480-5. doi: 10.1111/j.1751-1097.1997.tb08594.x.

Abstract

When melanin absorbs light energy, it can produce potentially damaging active oxygen species. There is little doubt that constitutive pigment in dark-skinned individuals is photoprotective against skin cancer, but induced pigment-as in tanning-may not be. The first step in cancer induction is mutation in DNA. The most suitable systems for evaluating the role of melanin are those in which pigment can be varied and mutations can be measured. Several cell lines from Cloudman S91 mouse melanoma can be induced to form large quantities of melanin pigment after treatment with a number of different agents enabling comparison of mutant yields in the same cells differing principally in pigment concentration. In these studies, melanin was induced with synthetic alpha-melanocyte-stimulating hormone and with isobutyl methyl xanthine in the cell line S91/mel. The former inducer produced about 50% more pigment than the latter. Survival and mutation induction at the Na+/K(+)-ATPase locus were studied using ethyl methane sulfonate (EMS), a standard mutagen and five UV lamps emitting near monochromatic and polychromatic UV light in the three wave-length ranges of UV. There was greater protection against killing and mutation induction in the more heavily pigmented cells after exposure to EMS and after irradiation with monochromatic UVC and UVB. There was significant protection against killing by polychromatic UVB + UVA (FS20), but the small degree of protection against mutation was not significant. No significant change in killing and mutation using the same protocol was seen in S91/amel, a related cell line that does not respond to these inducers. No mutants were produced by either monochromatic or polychromatic UVA at doses that killed 50% of the cells. Our results show that induced pigment-shown earlier to be eumelanin (K. A. Cieszka et al., Exp. Dermatol. 4, 192-198, 1995)-is photo- and chemoprotective, but it is less effective in protection against mutagenesis by polychromatic UVB + UVA in a spectrum that more nearly approximates the solar spectrum.

摘要

当黑色素吸收光能时,它会产生具有潜在破坏性的活性氧物质。毫无疑问,深色皮肤个体中的固有色素对皮肤癌具有光保护作用,但诸如晒黑产生的诱导性色素可能并非如此。癌症诱发的第一步是DNA突变。评估黑色素作用的最合适系统是那些色素含量可以变化且突变可以测量的系统。用多种不同试剂处理后,Cloudman S91小鼠黑色素瘤的几种细胞系可被诱导形成大量黑色素,从而能够比较主要在色素浓度上存在差异的同一细胞中的突变产量。在这些研究中,在细胞系S91/mel中用合成的α-黑素细胞刺激激素和异丁基甲基黄嘌呤诱导黑色素生成。前一种诱导剂产生的色素比后一种多约50%。使用标准诱变剂甲基磺酸乙酯(EMS)以及五盏在三个紫外线波长范围内发射近单色和多色紫外线的紫外线灯,研究了Na+/K(+)-ATP酶基因座处的细胞存活和突变诱导情况。在暴露于EMS后以及用单色UVC和UVB照射后,色素含量较高的细胞对杀伤和突变诱导具有更强的保护作用。对于多色UVB + UVA(FS20)的杀伤作用有显著保护,但对突变的保护程度较小,不具有显著性。在不响应这些诱导剂的相关细胞系S91/amel中,使用相同方案未观察到杀伤和突变有显著变化。在杀死50%细胞的剂量下,单色或多色UVA均未产生突变体。我们的结果表明,诱导性色素(先前已证明是真黑素,K. A. Cieszka等人,《实验皮肤病学》4,192 - 198,1995)具有光保护和化学保护作用,但在更接近太阳光谱的光谱中,它对多色UVB + UVA诱变的保护效果较差。

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