Fisetin, a Potent Anticancer Flavonol Exhibiting Cytotoxic Activity against Neoplastic Malignant Cells and Cancerous Conditions: A Scoping, Comprehensive Review

Nutrients. 2022 Jun 23;14(13):2604. doi: 10.3390/nu14132604.

Abstract

Diet plays a crucial role in homeostasis maintenance. Plants and spices containing flavonoids have been widely used in traditional medicine for thousands of years. Flavonols present in our diet may prevent cancer initiation, promotion and progression by modulating important enzymes and receptors in signal transduction pathways related to proliferation, differentiation, apoptosis, inflammation, angiogenesis, metastasis and reversal of multidrug resistance. The anticancer activity of fisetin has been widely documented in numerous in vitro and in vivo studies. This review summarizes the worldwide, evidence-based research on the activity of fisetin toward various types of cancerous conditions, while describing the chemopreventive and therapeutic effects, molecular targets and mechanisms that contribute to the observed anticancer activity of fisetin. In addition, this review synthesized the results from preclinical studies on the use of fisetin as an anticancer agent. Based on the available literature, it might be suggested that fisetin has a bioactive potential to become a complementary drug in the prevention and treatment of cancerous conditions. However, more in-depth research is required to validate current data, so that this compound or its derivatives can enter the clinical trial phase.

Keywords: anticancer; cancer; fisetin; flavonoid; flavonol.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents* / pharmacology
  • Antineoplastic Agents* / therapeutic use
  • Apoptosis
  • Cell Line, Tumor
  • Flavonoids / pharmacology
  • Flavonoids / therapeutic use
  • Flavonols / pharmacology
  • Flavonols / therapeutic use
  • Humans
  • Neoplasms* / drug therapy
  • Neoplasms* / prevention & control

Substances

  • Antineoplastic Agents
  • Flavonoids
  • Flavonols
  • fisetin

Grants and funding

This work was financially supported by the Medical University of Silesia in Katowice, Poland (Grant No. PCN-2-050/K/O/I and No. PCN-1-019/N/1/I).