Broad-Spectrum Preclinical Antitumor Activity of Chrysin: Current Trends and Future Perspectives

Biomolecules. 2020 Sep 27;10(10):1374. doi: 10.3390/biom10101374.

Abstract

Pharmacological profile of phytochemicals has attracted much attention to their use in disease therapy. Since cancer is a major problem for public health with high mortality and morbidity worldwide, experiments have focused on revealing the anti-tumor activity of natural products. Flavonoids comprise a large family of natural products with different categories. Chrysin is a hydroxylated flavonoid belonging to the flavone category. Chrysin has demonstrated great potential in treating different disorders, due to possessing biological and therapeutic activities, such as antioxidant, anti-inflammatory, hepatoprotective, neuroprotective, etc. Over recent years, the anti-tumor activity of chrysin has been investigated, and in the present review, we provide a mechanistic discussion of the inhibitory effect of chrysin on proliferation and invasion of different cancer cells. Molecular pathways, such as Notch1, microRNAs, signal transducer and activator of transcription 3 (STAT3), nuclear factor-kappaB (NF-κB), PI3K/Akt, MAPK, etc., as targets of chrysin are discussed. The efficiency of chrysin in promoting anti-tumor activity of chemotherapeutic agents and suppressing drug resistance is described. Moreover, poor bioavailability, as one of the drawbacks of chrysin, is improved using various nanocarriers, such as micelles, polymeric nanoparticles, etc. This updated review will provide a direction for further studies in evaluating the anti-tumor activity of chrysin.

Keywords: cancer therapy; chemotherapy; chrysin; flavonoid; nanoparticle.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Antioxidants / therapeutic use
  • Drug Resistance, Neoplasm / drug effects*
  • Flavonoids / therapeutic use*
  • Humans
  • MicroRNAs / genetics
  • Neoplasms / drug therapy*
  • Neoplasms / genetics
  • Neoplasms / pathology
  • Receptor, Notch1 / genetics
  • STAT3 Transcription Factor / genetics
  • Signal Transduction / drug effects

Substances

  • Antineoplastic Agents
  • Antioxidants
  • Flavonoids
  • MicroRNAs
  • Receptor, Notch1
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • chrysin