Synthesis and biological properties of polyamine modified flavonoids as hepatocellular carcinoma inhibitors

Eur J Med Chem. 2016 Oct 4:121:110-119. doi: 10.1016/j.ejmech.2016.04.031. Epub 2016 May 19.

Abstract

A series of polyamine conjugates of flavonoids with a naphthalene motif were synthesized and evaluated for their anti-hepatocellular carcinoma properties using in vitro and in vivo assays. Compound 8a displayed favorable selectivity between hepatocellular carcinoma cells and normal hepatocyte cells, and the combination of 8a with aspirin resulted in additive inhibition of in vitro tumor cell growth and migration. The 8a-aspirin combination also inhibited H22 liver tumor growth and pulmonary metastasis and improved body weight index in animal models. Preliminary mechanistic studies indicated that 8a increased the expression of apoptosis-related proteins such as p-p38, p-JNK, p53 and Bcl-2, an effect that was further amplified by aspirin. Therefore, a cocktail therapy of flavonoid-polyamine conjugates with aspirin has potential use as an antitumor therapy.

Keywords: Antitumor; Flavonoids; Polyamine; Synthesis.

MeSH terms

  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Apoptosis Regulatory Proteins / drug effects
  • Aspirin / therapeutic use
  • Carcinoma, Hepatocellular / drug therapy*
  • Cell Line / pathology
  • Flavonoids / chemical synthesis
  • Flavonoids / pharmacology*
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / pathology
  • Neoplasm Metastasis
  • Polyamines / chemistry
  • Polyamines / pharmacology

Substances

  • Apoptosis Regulatory Proteins
  • Flavonoids
  • Polyamines
  • Aspirin