Therapeutic potential of chrysin nanoparticle-mediation inhibition of succinate dehydrogenase and ubiquinone oxidoreductase in pancreatic and lung adenocarcinoma

Eur J Med Res. 2022 Sep 8;27(1):172. doi: 10.1186/s40001-022-00803-y.

Abstract

Pancreatic adenocarcinoma (PDAC) and lung cancer are expected to represent the most common cancer types worldwide until 2030. Under typical conditions, mitochondria provide the bulk of the energy needed to sustain cell life. For that inhibition of mitochondrial complex ΙΙ (CΙΙ) and ubiquinone oxidoreductase with natural treatments may represent a promising cancer treatment option. A naturally occurring flavonoid with biological anti-cancer effects is chyrsin. Due to their improved bioavailability, penetrative power, and efficacy, chitosan-chrysin nano-formulations (CCNPs) are being used in medicine with increasing frequency. Chitosan (cs) is also regarded as a highly versatile and adaptable polymer. The cationic properties of Cs, together with its biodegradability, high adsorption capacity, biocompatibility, effect on permeability, ability to form films, and adhesive properties, are advantages. In addition, Cs is thought to be both safe and economical. CCNPs may indeed be therapeutic candidates in the treatment of pancreatic adenocarcinoma (PDAC) and lung cancer by blocking succinate ubiquinone oxidoreductase.

Keywords: Cancer; Chitosan; Chrysin; Mitochondria; Succinate dehydrogenase.

Publication types

  • Review

MeSH terms

  • Adenocarcinoma of Lung* / drug therapy
  • Adenocarcinoma* / drug therapy
  • Chitosan* / pharmacology
  • Flavonoids
  • Humans
  • Lung Neoplasms* / drug therapy
  • Nanoparticles*
  • Pancreatic Neoplasms* / drug therapy
  • Succinate Dehydrogenase / metabolism
  • Ubiquinone

Substances

  • Flavonoids
  • Ubiquinone
  • chrysin
  • Chitosan
  • Succinate Dehydrogenase