Organic selenium compounds as potential chemotherapeutic agents for improved cancer treatment

Valentina Gandin1, Prajakta Khalkar2, Jeremy Braude1

  • 1Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Via Marzolo 5, 35131 Padova, Italy.

Insights

Selenium compounds show promise as anticancer agents, selectively targeting cancer cells. Organoselenium compounds, both natural and synthetic, offer potent antitumor activity with potentially fewer side effects, warranting further research into their mechanisms.

Area of Science:

  • Biochemistry
  • Pharmacology
  • Oncology

Background:

  • Selenium (Se)-containing compounds are increasingly recognized for their anticancer potential.
  • These compounds exhibit high efficacy and selectivity against various cancer cells.
  • Their cytotoxic effects often involve acting as pro-oxidants, disrupting cellular redox homeostasis.

Purpose of the Study:

  • To review natural and synthetic organoselenium compounds with anticancer activity.
  • To summarize recent advancements in understanding their molecular anticancer mechanisms.
  • To highlight the therapeutic potential of organoselenium compounds in cancer treatment.

Main Methods:

  • Literature review of natural and synthetic organoselenium compounds.
  • Analysis of studies on their cytotoxic effects and mechanisms of action.
  • Examination of their impact on cellular redox homeostasis and signaling pathways.

Main Results:

  • Organoselenium compounds demonstrate significant antitumor activity, including metastasis prevention.
  • Natural organoselenium compounds may possess fewer side effects compared to inorganic selenium compounds.
  • The specific mechanisms of action and cell death pathways are dependent on the compound's chemical properties and the cancer model.

Conclusions:

  • Organoselenium compounds represent a promising class of anticancer agents.
  • Further research into their molecular mechanisms can facilitate the development of novel chemotherapeutics.
  • Their potential for reduced systemic toxicity warrants continued investigation for clinical applications.

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