Natural and Synthetic Flavonoids: Structure–Activity Relationship and Chemotherapeutic Potential for the Treatment of Leukemia

José C.J.M.D.S. Menezes, Barbora Orlikova, Franck Morceau, Marc Diederich*

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

76 Citations (Scopus)

Abstract

Flavonoids and their derivatives are polyphenolic secondary metabolites with an extensive spectrum of pharmacological activities, including antioxidants, antitumor, anti-inflammatory, and antiviral activities. These flavonoids can also act as chemopreventive agents by their interaction with different proteins and can play a vital role in chemotherapy, suggesting a positive correlation between a lower risk of cancer and a flavonoid-rich diet. These agents interfere with the main hallmarks of cancer by various individual mechanisms, such as inhibition of cell growth and proliferation by arresting the cell cycle, induction of apoptosis and differentiation, or a combination of these mechanisms. This review is an effort to highlight the therapeutic potential of natural and synthetic flavonoids as anticancer agents in leukemia treatment with respect to the structure–activity relationship (SAR) and their molecular mechanisms. Induction of cell death mechanisms, production of reactive oxygen species, and drug resistance mechanisms, including p-glycoprotein efflux, are among the best-described effects triggered by the flavonoid polyphenol family.

Original languageEnglish
Pages (from-to)S4-S28
JournalCritical Reviews in Food Science and Nutrition
Volume56
DOIs
Publication statusPublished - 29 Jul 2016
Externally publishedYes

Keywords

  • apoptosis
  • caspase
  • chemoprevention
  • cytotoxic
  • Flavonoids
  • leukemia
  • mitochondria
  • P-glycoprotein
  • PARP
  • ROS
  • SAR

Fingerprint

Dive into the research topics of 'Natural and Synthetic Flavonoids: Structure–Activity Relationship and Chemotherapeutic Potential for the Treatment of Leukemia'. Together they form a unique fingerprint.

Cite this