Flavonoids as regulators of TIMPs expression in cancer: Consequences, opportunities, and challenges

Life Sci. 2022 Nov 1:308:120932. doi: 10.1016/j.lfs.2022.120932. Epub 2022 Sep 5.

Abstract

Cancer is one of the leading causes of death in patients worldwide, where invasion and metastasis are directly responsible for this statement. Although cancer therapy has progressed in recent years, current therapeutic approaches are ineffective due to toxicity and chemoresistance. Therefore, it is essential to evaluate other treatment options, and natural products are a promising alternative as they show antitumor properties in different study models. This review describes the regulation of tissue inhibitors of metalloproteinases (TIMPs) expression and the role of flavonoids as molecules with the antitumor activity that targets TIMPs therapeutically. These inhibitors regulate tissue extracellular matrix (ECM) turnover; they inhibit matrix metalloproteinases (MMPs), cell migration, invasion, and angiogenesis and induce apoptosis in tumor cells. Data obtained in cell lines and in vivo models suggest that flavonoids are chemopreventive and cytotoxic against various types of cancer through several mechanisms. Flavonoids also regulate crucial signaling pathways such as focal adhesion kinase (FAK), phosphatidylinositol-3-kinase (PI3K)-Akt, signal transducer and activator of transcription 3 (STAT3), nuclear factor κB (NFκB), and mitogen-activated protein kinase (MAPK) involved in cancer cell migration, invasion, and metastasis. All these data reposition flavonoids as excellent candidates for use in cancer therapy.

Keywords: Cancer; Flavonoids; Matrix metalloproteinases; Metastasis; Tissue inhibitor of metalloproteinases.

Publication types

  • Review

MeSH terms

  • Biological Products*
  • Flavonoids / pharmacology
  • Flavonoids / therapeutic use
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Humans
  • Matrix Metalloproteinases / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Neoplasms* / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphatidylinositols
  • Proto-Oncogene Proteins c-akt / metabolism
  • STAT3 Transcription Factor / metabolism
  • Tissue Inhibitor of Metalloproteinases / metabolism*

Substances

  • Biological Products
  • Flavonoids
  • NF-kappa B
  • Phosphatidylinositols
  • STAT3 Transcription Factor
  • Tissue Inhibitor of Metalloproteinases
  • Focal Adhesion Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinases
  • Matrix Metalloproteinases