Metal-induced toxicity, carcinogenesis, mechanisms and cellular responses

Mol Cell Biochem. 2004 Jan;255(1-2):3-10. doi: 10.1023/b:mcbi.0000007255.72746.a6.

Abstract

A wide variety of metals have been reported to act as mutagenic and carcinogenic agents in both human and animal studies. The underlying mechanisms are being extensively investigated. Recently, a new sub-discipline of molecular carcinogenesis has surfaced and new techniques and instruments are being developed which allow exploration of the complex biological relationships and signaling pathways involved in response to metal exposure at the molecular level. The 2nd Conference on Molecular Mechanisms of Metal Toxicity and Carcinogenesis was held at NIOSH in Morgantown, West Virginia, Sept. 8-11, 2002. One hundred thirty scientist from sixteen countries presented their novel findings and investigations of metal-induced carcinogenesis. The conference focused on state-of-the-art research and developments in metal toxicity and carcinogenesis. Emphasis was placed on delineating molecular mechanisms involved in free radical effects, cellular uptake, signaling pathways/interaction, dose response, biomarkers, and resistance mechanisms. This article reviews some of the novel information presented at the conference and discusses future avenues of research in this field.

Publication types

  • Review

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Carcinogens / toxicity*
  • Cell Cycle / drug effects
  • Cell Division / drug effects
  • Cell Transformation, Neoplastic / chemically induced*
  • DNA Adducts / metabolism
  • DNA Damage
  • DNA Repair
  • Free Radicals / metabolism
  • Gene Expression / drug effects
  • Humans
  • Metals / metabolism
  • Metals / toxicity*
  • Mice
  • Mutagens / toxicity*
  • Neoplasms / chemically induced
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects
  • Transcription Factors / drug effects
  • Transcription Factors / physiology

Substances

  • Carcinogens
  • DNA Adducts
  • Free Radicals
  • Metals
  • Mutagens
  • Reactive Oxygen Species
  • Transcription Factors