[Role of clock proteins in skin carcinogenesis in 14-month-old SHR mice maintained under disrupted light regimen]

Vopr Onkol. 2016;62(5):666-670.
[Article in Russian]

Abstract

Circadian rhythm disturbance promotes of carcinogenesis and is associated with changes in clock genes and proteins expression. In the current study we observed that continu- ous light exposure potentiated skin carcinogenesis induced by 7,12-dimethylbenz[a]anthracene and 12-0-tetradecanoylphor- bol-13-acetate while melatonin had opposite effect. Carcinogenic exposure decreased BMAL1 and CRYI- expression in the skin, CLOCK expression was upregulated and CRYl downregulated in tumor compared to normal skin. BMAL1 expression increased under disrupted light regimen; melatonin treatment affected CLOCK expression in tumors and CRYI in skin at the carcinogens application sites.

MeSH terms

  • 9,10-Dimethyl-1,2-benzanthracene / toxicity
  • ARNTL Transcription Factors / biosynthesis
  • Animals
  • CLOCK Proteins / biosynthesis*
  • Cell Transformation, Neoplastic / chemically induced
  • Cell Transformation, Neoplastic / metabolism*
  • Cell Transformation, Neoplastic / pathology
  • Cryptochromes / biosynthesis
  • Gene Expression Regulation, Neoplastic*
  • Lighting*
  • Male
  • Mice
  • Neoplasm Proteins / biosynthesis*
  • Skin Neoplasms / chemically induced
  • Skin Neoplasms / metabolism*
  • Skin Neoplasms / pathology
  • Tetradecanoylphorbol Acetate / toxicity

Substances

  • ARNTL Transcription Factors
  • Bmal1 protein, mouse
  • Cry1 protein, mouse
  • Cryptochromes
  • Neoplasm Proteins
  • 9,10-Dimethyl-1,2-benzanthracene
  • CLOCK Proteins
  • Clock protein, mouse
  • Tetradecanoylphorbol Acetate