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DNA damage and somatic mutations in mammalian cells after irradiation with a nail polish dryer.
Zhivagui, Maria; Hoda, Areebah; Valenzuela, Noelia; Yeh, Yi-Yu; Dai, Jason; He, Yudou; Nandi, Shuvro P; Otlu, Burcak; Van Houten, Bennett; Alexandrov, Ludmil B.
Affiliation
  • Zhivagui M; Department of Cellular and Molecular Medicine, UC San Diego, La Jolla, CA, 92093, USA.
  • Hoda A; Department of Bioengineering, UC San Diego, La Jolla, CA, 92093, USA.
  • Valenzuela N; Moores Cancer Center, UC San Diego, La Jolla, CA, 92037, USA.
  • Yeh YY; Department of Cellular and Molecular Medicine, UC San Diego, La Jolla, CA, 92093, USA.
  • Dai J; Moores Cancer Center, UC San Diego, La Jolla, CA, 92037, USA.
  • He Y; Department of Bioengineering, UC San Diego, La Jolla, CA, 92093, USA.
  • Nandi SP; Department of Bioengineering, UC San Diego, La Jolla, CA, 92093, USA.
  • Otlu B; Department of Cellular and Molecular Medicine, UC San Diego, La Jolla, CA, 92093, USA.
  • Van Houten B; Department of Bioengineering, UC San Diego, La Jolla, CA, 92093, USA.
  • Alexandrov LB; Moores Cancer Center, UC San Diego, La Jolla, CA, 92037, USA.
Nat Commun ; 14(1): 276, 2023 01 17.
Article in En | MEDLINE | ID: mdl-36650165
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, no experimental evaluation has been conducted to reveal the effect of radiation emitted by UV-nail polish dryers on mammalian cells. 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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Ultraviolet Rays / DNA Damage / Fibroblasts Limits: Animals / Humans Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Ultraviolet Rays / DNA Damage / Fibroblasts Limits: Animals / Humans Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2023 Type: Article Affiliation country: United States