L-cysteine as a regulator for arsenic-mediated cancer-promoting and anti-cancer effects

Toxicol In Vitro. 2011 Apr;25(3):623-9. doi: 10.1016/j.tiv.2010.12.012. Epub 2010 Dec 30.

Abstract

Previous studies have shown that activities of tyrosine kinases and secretion of the active form of matrix metalloproteinase-2 (MMP-2) are correlated with promotion of tumor growth, while apoptotic cell death in cancer cells is correlated with anti-cancer effects. Although arsenic has been reported to have both cancer-promoting and anti-cancer effects, the mechanisms of the arsenic-mediated bidirectional effects remain unknown. We examined the effects of arsenic on both proto-oncogene c-RET-transfected NIH3T3 cells with benign characters and oncogenic RET-MEN2A-transfected NIH3T3 cells with malignant characters. Arsenic promoted not only c-RET tyrosine kinase activity but also genetically activated RET-MEN2A kinase activity with promotion of dimer formation of RET proteins. Arsenic also increased secretion of the active form of MMP-2 in both RET-MEN2A-transfectants and c-RET-transfectants. On the other hand, arsenic promoted poly-(ADP-ribose) polymerase (PARP) degradation and cell death in both malignant and non-malignant cells. Interestingly, l-cysteine inhibited the arsenic-mediated tumor-promoting effects (activation of kinases and MMP-2 secretion) but not arsenic-mediated anti-cancer effects (PARP degradation and cell death). Our results suggest redox-linked regulation of arsenic-mediated activities of kinases and MMP-2 secretion but not arsenic-mediated cell death. Our results also suggest that l-cysteine is an ideal supplement that inhibits arsenic-mediated tumor-promoting effects without affecting arsenic-mediated anti-cancer effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticarcinogenic Agents / toxicity*
  • Arsenites / toxicity*
  • Carcinogens, Environmental / toxicity*
  • Cell Survival / drug effects
  • Cysteine / pharmacology*
  • Drug Interactions
  • Enzyme Inhibitors / toxicity*
  • Matrix Metalloproteinase 2 / metabolism
  • Mice
  • Multiple Endocrine Neoplasia Type 2a / genetics
  • NIH 3T3 Cells / drug effects*
  • NIH 3T3 Cells / metabolism
  • NIH 3T3 Cells / pathology
  • Poly(ADP-ribose) Polymerases / metabolism
  • Sodium Compounds / toxicity*
  • Transfection

Substances

  • Anticarcinogenic Agents
  • Arsenites
  • Carcinogens, Environmental
  • Enzyme Inhibitors
  • Sodium Compounds
  • sodium arsenite
  • Poly(ADP-ribose) Polymerases
  • Matrix Metalloproteinase 2
  • Cysteine