[Arachidonic acid and prostaglandins, inflammation and oncology]

Presse Med. 2001 Mar 17;30(10):508-10.
[Article in French]

Abstract

CYCLOOXYGENASE PATHWAY: Among the 3 metabolic pathways leading to oxidation of arachidonic acid, the cyclooxygenase (COX) pathway produces prostaglandin G2 that is rapidly transformed into prostaglandin H2. PROSTAGLANDINS: Prostaglandins are inflammation mediators that are strongly implicated in tumorgenesis. They participate in tumor initiation, promotion and growth. INFLAMMATION AND EPITHELIAL CANCER: Chronic inflammation is a risk factor for epithelial cancer. It induces prostaglandin synthesis via activation of COX-2. There is a cause and effect relationship between chronic inflammation and carcinogeneis via COX-2 expression. It has been demonstrated that COX-2 favors tumor invasion and inhibits apoptosis. Tumor growth is favored by PGE2-induced reduction in immunity; COX-2 inhibitors reinforce the immune response. Finally COX-2 is expressed in tumor neovessels and plays a role in angiogenesis.

Publication types

  • English Abstract

MeSH terms

  • Arachidonic Acid / pharmacology*
  • Carcinoma / etiology*
  • Carcinoma / physiopathology
  • Cell Transformation, Neoplastic
  • Cyclooxygenase 2
  • Humans
  • Inflammation / physiopathology*
  • Isoenzymes / biosynthesis
  • Isoenzymes / metabolism*
  • Membrane Proteins
  • Neoplasms, Glandular and Epithelial / etiology*
  • Neoplasms, Glandular and Epithelial / physiopathology
  • Neovascularization, Pathologic
  • Oxidation-Reduction
  • Prostaglandin-Endoperoxide Synthases / biosynthesis
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • Prostaglandins / metabolism*

Substances

  • Isoenzymes
  • Membrane Proteins
  • Prostaglandins
  • Arachidonic Acid
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases