DNA damage and somatic mutations in mammalian cells after irradiation with a nail polish dryer

被引:19
作者
Zhivagui, Maria [1 ,2 ,3 ]
Hoda, Areebah [1 ]
Valenzuela, Noelia [3 ]
Yeh, Yi-Yu [2 ]
Dai, Jason [2 ]
He, Yudou [1 ,2 ,3 ]
Nandi, Shuvro P. [1 ,2 ,3 ]
Otlu, Burcak [1 ,2 ,3 ]
Van Houten, Bennett [4 ]
Alexandrov, Ludmil B. [1 ,2 ,3 ]
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92037 USA
[4] Univ Pittsburgh, UPMC Hillman Canc Ctr, Pittsburgh, PA 15213 USA
关键词
ULTRAVIOLET-A RADIATION; CARCINOGENIC RISKS; CELLULAR-DNA; UVA; SIGNATURES; TUMORIGENESIS; VISUALIZATION; MUTAGENICITY; MUTAGENESIS; PATTERNS;
D O I
10.1038/s41467-023-35876-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nail polish dryers commonly emit ultraviolet A (UVA) light, but the effects of this irradiation on mammalian cells remain unclear. Here, the authors examine the effects of UVA irradiation by a nail polish dryer on the genomes of mammalian cell lines, finding high levels of reactive oxygen species and related mutational signatures. Ultraviolet A light is commonly emitted by UV-nail polish dryers with recent reports suggesting that long-term use may increase the risk for developing skin cancer. However, the effect of radiation emitted by UV-nail polish dryers on the physiology and mutagenesis of mammalian cells remains unclear. Here, we show that irradiation by a UV-nail polish dryer causes high levels of reactive oxygen species, consistent with 8-oxo-7,8-dihydroguanine damage and mitochondrial dysfunction. Analysis of somatic mutations reveals a dose-dependent increase of C:G>A:T substitutions in irradiated samples with mutagenic patterns similar to mutational signatures previously attributed to reactive oxygen species. In summary, this study demonstrates that radiation emitted by UV-nail polish dryers can both damage DNA and permanently engrave mutations on the genomes of primary mouse embryonic fibroblasts, human foreskin fibroblasts, and human epidermal keratinocytes.
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页数:14
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