Related Experiment Video
Updated: Aug 29, 2026

Anticancer Metal Complexes: Synthesis and Cytotoxicity Evaluation by the MTT Assay
Published on: November 10, 2013
Metals and metal compounds in carcinogenesis
1Laboratoire de Biochimie et de Biologie Moléculaire, Faculté de Pharmacie, 51 rue Cognac-Jay, IFR-53, EA 3306, 51096 Reims, France. bernard.desoize@univ-reims.fr
Abstract:
Several metals and metal containing compounds are potent mutagens and carcinogens. The most often blamed are chromium, arsenic, nickel, vanadium, iron, copper and manganese. Although each of them has its own mechanism of action, it is believed that most of their mechanisms of action involve reactive oxygen species (ROS). Furthermore, nickel modulates gene expression by induction of DNA methylation and/or suppression of histone acetylation. Arsenic activity on cell metabolism is multiple; it seems that cell transformation is induced by long-term exposure to a low level of arsenic. The paradox of arsenic is that it has also a valuable therapeutic efficacy in cancer treatment. Manganese is known to cause DNA damage, although it does not represent a significant carcinogenic risk. Magnesium deficiency and iron excess are not exactly carcinogenetic, but certain concentrations of these metal ions are needed to prevent cancer.
Insights
Several metals like chromium, arsenic, and nickel are potent mutagens and carcinogens, often acting through reactive oxygen species (ROS). While some metals pose risks, others like arsenic also show therapeutic potential in cancer treatment.
Area of Science:
- Environmental toxicology
- Molecular carcinogenesis
- Metal-induced toxicity
Background:
- Certain metals and metal compounds are recognized as significant mutagens and carcinogens.
- Chromium, arsenic, nickel, vanadium, iron, copper, and manganese are frequently implicated in such effects.
Purpose of the Study:
- To explore the mechanisms by which metals induce mutagenicity and carcinogenicity.
- To highlight the dual role of certain metals, such as arsenic, in both causing and treating cancer.
Main Methods:
- Review of existing literature on metal toxicity and carcinogenicity.
- Analysis of proposed mechanisms involving reactive oxygen species (ROS).
- Examination of specific metal effects, including nickel's modulation of gene expression and arsenic's impact on cell metabolism.
Main Results:
- Most metal-induced mechanisms are believed to involve reactive oxygen species (ROS).
- Nickel can alter gene expression through DNA methylation and histone acetylation changes.
- Long-term, low-level arsenic exposure may induce cell transformation, yet arsenic also possesses anti-cancer therapeutic properties.
- Manganese can cause DNA damage but has a low carcinogenic risk; magnesium deficiency and iron excess are linked to cancer risk.
Conclusions:
- Metals play a complex role in carcinogenesis, with diverse mechanisms.
- Understanding these mechanisms is crucial for both prevention and therapeutic strategies.
- The dual nature of some metals, like arsenic, warrants further investigation for cancer treatment applications.
Related Concept Videos
Mutagenicity and Carcinogenicity
Properties of Organometallic Compounds
Cancer Prevention
Some...
The Periodic Table and Organismal Elements
Periodic Table Provides Information...
Bioactivation and Tissue Toxicity
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...

