Role of Induced Programmed Cell Death in the Chemopreventive Potential of Apigenin

Int J Mol Sci. 2022 Mar 29;23(7):3757. doi: 10.3390/ijms23073757.

Abstract

The flavonoid apigenin (4',5,7-trihydroxyflavone), which is one of the most widely distributed phytochemicals in the plant kingdom, is one of the most thoroughly investigated phenolic components. Previous studies have attributed the physiological effects of apigenin to its anti-allergic, antibacterial, antidiabetic, anti-inflammatory, antioxidant, antiviral, and blood-pressure-lowering properties, and its documented anticancer properties have been attributed to the induction of apoptosis and autophagy, the inhibition of inflammation, angiogenesis, and cell proliferation, and the regulation of cellular responses to oxidative stress and DNA damage. The most well-known mechanism for the compound's anticancer effects in human cancer cell lines is apoptosis, followed by autophagy, and studies have also reported that apigenin induces novel cell death mechanisms, such as necroptosis and ferroptosis. Therefore, the aim of this paper is to review the therapeutic potential of apigenin as a chemopreventive agent, as well as the roles of programmed cell death mechanisms in the compound's chemopreventive properties.

Keywords: apigenin; apoptosis; autophagy; ferroptosis; necroptosis.

Publication types

  • Review

MeSH terms

  • Apigenin* / pharmacology
  • Apigenin* / therapeutic use
  • Apoptosis*
  • Autophagy
  • Cell Line, Tumor
  • Cell Proliferation
  • DNA Damage
  • Humans

Substances

  • Apigenin