Inorganic arsenic exposure increased expression of Fas and Bax gene in vivo and vitro

Gene. 2018 Sep 10:671:135-141. doi: 10.1016/j.gene.2018.05.121. Epub 2018 Jun 1.

Abstract

Accumulating evidences have shown that apoptosis plays an important role in mediating the therapeutic effects and toxicity of arsenic. Fas and Bax genes are critical regulatory genes for apoptosis. In this study, we investigated the association between levels of Fas and Bax expression and the three arsenic species (inorganic arsenic (iAs), monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA)) in vivo and vitro. Three arsenic species in urine were measured and levels of Fas and Bax expression were examined by the quantitative real-time PCR (qPCR) for all subjects. We found that Fas and Bax mRNA expression in the exposed group were significantly higher than that in the control group. The levels of gene expression were positively correlated with the concentrations of urinary iAs, MMA and DMA in all subjects. Sodium arsenite induced Fas and Bax mRNA expression, then MMA and DMA did not induce mRNA expression in MDA-MB-231 and XWLC-05 cells. The findings of the present study indicated that iAs, MMA, and DMA had different effects on expression of Bax and Fas gene.

Keywords: Arsenic; Bax; DMA Fas; MMA.

MeSH terms

  • Arsenic / toxicity
  • Arsenic / urine*
  • Arsenic Poisoning / genetics*
  • Arsenic Poisoning / urine
  • Arsenicals / urine
  • Cacodylic Acid / toxicity
  • Cacodylic Acid / urine
  • Cell Line, Tumor
  • Female
  • Gene Expression Regulation / drug effects
  • Humans
  • Male
  • Occupational Exposure
  • Up-Regulation*
  • bcl-2-Associated X Protein / genetics*
  • fas Receptor / genetics*

Substances

  • Arsenicals
  • BAX protein, human
  • FAS protein, human
  • bcl-2-Associated X Protein
  • fas Receptor
  • Cacodylic Acid
  • monomethylarsonic acid
  • Arsenic