mTOR Targeted Cancer Chemoprevention by Flavonoids

Curr Med Chem. 2021;28(39):8068-8082. doi: 10.2174/0929867327666201109122025.

Abstract

Over the past several decades, plant-derived products (phytochemicals) have been suggested to possess immense therapeutic potential. Among these phytochemicals, different flavonoids have been reported for their potent anticancer activity. To exhibit their anticancer potential, these flavonoids modulate different signaling pathways. Among these pathways, the mammalian target of rapamycin (mTOR) and associated phosphatidyl-inositol 3-kinase (PI3K)/protein kinase B (Akt) signaling cascade have been reported as a pivotal modulator of cell survival, proliferation, and death/apoptosis. Hence, targeting this cascade could be an ideal strategy to alleviate apoptosis and inhibit proliferation in different forms of cancer. The targeting of PI3K/Akt/mTOR by flavonoids have been well documented in the scientific literature. In the current study, we have studied the anticancer potential of various flavonoids, especially flavones, flavonols, and isoflavones that include apigenin, luteolin, baicalein, tangeretin, epigallocatechin- 3-gallate, genistein, and daidzein especially dealing with mTOR targeting.

Keywords: Apigenin; baicalein; cancer prevention; daidzein; epigallocatechin-3-gallate; flavonoids; genistein; luteolin; mTOR.; tangeretin.

Publication types

  • Review

MeSH terms

  • Chemoprevention
  • Flavonoids* / pharmacology
  • Flavonoids* / therapeutic use
  • Humans
  • Neoplasms* / drug therapy
  • Neoplasms* / prevention & control
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases

Substances

  • Flavonoids
  • MTOR protein, human
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases