Cellular toxicity of organotellurans: a systematic review of pre-clinical studies

Maria Luisa Lima Barreto do Nascimento1, Isabela Ribeiro de Sá Guimarães Nolêto2,3, Francisco Leonardo Torres-Leal4

  • 1Laboratory of Genetical Toxicology, Postgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Piauí, 64.049-550, Brazil. mlbarreto95@gmail.com.

Insights

Organotellurans show promise as anticancer agents due to their cytotoxic effects on cancer cells. Further research is needed to optimize efficacy and address toxicity concerns for these organometallic compounds.

Area of Science:

  • Medicinal Chemistry
  • Toxicology
  • Pharmacology

Background:

  • Organotellurans, organometallic compounds containing tellurium, are gaining attention for their unique structures and potential therapeutic uses.
  • Despite potential pharmacological applications, organotellurans also present toxicity risks that warrant investigation.

Purpose of the Study:

  • To evaluate the cytotoxic effects of organotellurans as potential anticancer agents.
  • To examine the cellular and genetic mechanisms underlying their action.
  • To assess toxicity in preclinical studies.

Main Methods:

  • A systematic literature search identified 32 articles.
  • Reviewed studies investigated 30 distinct organotelluran molecules.
  • Data from cell lines and in vivo experiments were analyzed.

Main Results:

  • Most studies demonstrated significant cytotoxic potential of organotellurans against various cancer cell lines.
  • Observed cytotoxic effects were dose-dependent.
  • Mechanisms included cell cycle arrest, caspase upregulation, mitochondrial dysfunction, and genotoxicity.

Conclusions:

  • Organotellurans exhibit considerable cytotoxic potential against cancer cells, supporting their development as anticancer agents.
  • Further research is essential to elucidate mechanisms, enhance efficacy, and mitigate toxicity.
  • Careful evaluation of cytotoxic effects and toxicity profiles is crucial for future organotelluran drug development.