Arsenic induces gender difference of estrogen receptor in AECII cells from ICR fetal mice

Toxicol In Vitro. 2019 Apr:56:133-140. doi: 10.1016/j.tiv.2019.01.014. Epub 2019 Jan 23.

Abstract

Arsenic is a confirmed human lung carcinogen with estrogenic activity. There are gender differences in the incidence of lung cancer. Estrogen receptors (ER) play an important role in the process of the development of lung cancer. In order to understand the gender difference effects of ER during carcinogenesis of lung induced by arsenic, the effects of arsenic and estrogen receptor antagonist (ICI182780) on expression levels of estrogen receptor beta (ERβ), extracellular regulated protein kinase (ERK1/2) and nuclear factor κB (NF-κB/P65) in type II alveolar epithelial cells (AECII) from different sex ICR fetal mice lung were detected. Results showed that arsenic increased the expression levels of mRNA and protein of ERβ, ERK1/2 and NF-κB/P65, and ICI182780 inhibited the increase. Furthermore, there remains a gender difference in these changes. To summarize, the observations here strongly suggested that estrogen receptor and its mediated signal pathway molecules might have critical roles of the gender difference of incidence of lung cancer in arsenic induced.

Keywords: Estrogen receptor β; Gender difference; Lung cancer; Mice; Sodium arsenite; TypeII alveolar epithelial cells.

MeSH terms

  • Alveolar Epithelial Cells / drug effects*
  • Alveolar Epithelial Cells / metabolism
  • Animals
  • Arsenic / toxicity*
  • Cells, Cultured
  • Endocrine Disruptors / toxicity*
  • Estrogen Receptor beta / genetics
  • Estrogen Receptor beta / metabolism*
  • Estrogens / toxicity*
  • Female
  • Fetus
  • MAP Kinase Signaling System / drug effects
  • Male
  • Mice, Inbred ICR
  • NF-kappa B / genetics
  • Sex Characteristics

Substances

  • Endocrine Disruptors
  • Estrogen Receptor beta
  • Estrogens
  • NF-kappa B
  • Arsenic