Rosmarinus officinalis L. as Fascinating Source of Potential Anticancer Agents Targeting Aromatase and COX-2: An

Adriana Gargano1,2, Ilario Greco1,2, Carmine Lupia3,4

  • 1Dipartimento di Scienze della Salute, Università degli Studi "Magna Græcia" di Catanzaro, Campus "S. Venuta", Viale Europa, 88100 Catanzaro, Italy.

Insights

This review explores Rosmarinus officinalis L. compounds as potential anticancer agents. These natural compounds may inhibit key enzymes, aromatase and cyclooxygenase-2, often upregulated in various cancers.

Area of Science:

  • Pharmacology and Oncology
  • Natural Product Chemistry

Background:

  • Cancer is a leading global cause of death.
  • Aromatase and cyclooxygenase-2 (COX-2) enzymes are frequently upregulated in numerous cancer types.
  • Natural compounds, particularly phytocompounds, have a significant history in cancer chemotherapy, often by interacting with key enzymes.

Purpose of the Study:

  • To review the role of main compounds from Rosmarinus officinalis L. as potential anticancer agents.
  • To investigate the interaction of these phytocompounds with aromatase and COX-2 enzymes.

Main Methods:

  • Literature review of scientific evidence on Rosmarinus officinalis L. compounds.
  • Analysis of studies reporting the interaction of phytocompounds with aromatase and COX-2.
  • Focus on compounds within Rosmarinus officinalis L.

Main Results:

  • Rosmarinus officinalis L. is rich in phytocompounds with demonstrated enzyme-inhibiting properties.
  • Several compounds from this medicinal plant show potential for interacting with and inhibiting aromatase and COX-2.
  • These interactions suggest a role in anticancer activity.

Conclusions:

  • Compounds from Rosmarinus officinalis L. show promise as natural anticancer agents.
  • Targeting aromatase and COX-2 with these phytocompounds represents a potential therapeutic strategy.
  • Further research into Rosmarinus officinalis L. for cancer treatment is warranted.