Oxidative damage and transforming growth factor beta 1 expression in pretumoral and tumoral lesions of human intestine

Free Radic Biol Med. 1997;22(5):889-94. doi: 10.1016/s0891-5849(96)00481-9.


The aim of this study was to evaluate a possible relationship between oxidative stress and transforming growth factor beta 1 (TGF beta 1) expression in human colon adenocarcinoma. Crohn's disease, an inflammatory pathology of the intestine often regarded to as precancerous, was also examined. Indices of impaired redox balance were monitored in blood and in bioptic samples from 10 adult patients with adenocarcinoma of the colon and from five patients with Crohn's disease. On tissue samples TGF beta 1 mRNA expression was also determined. Ten healthy adults provided normal reference values for plasma indices of oxidative stress, and normal tissue distant from the lesions was used for comparative analysis. Fluorescent adducts with plasma proteins of malonaldehyde (MDA) and 4-hydroxynonenal (HNE) were significantly lower than controls in the plasma from cancer patients and significantly higher in the plasma from Crohn's patients. In adenocarcinoma biopsies, susceptibility to lipid peroxidation processes and TGF beta 1 expression were below the relative control; in Crohn's disease, lipid peroxidation and cytokine expression were both above the relative control. The findings obtained suggest the existence of an association between oxidative damage and fibrogenic cytokine expression in the human intestine. Further studies are needed to conclusively prove the correlation between the two events.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / metabolism*
  • Adult
  • Aged
  • Aged, 80 and over
  • Case-Control Studies
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / metabolism*
  • Crohn Disease / genetics
  • Crohn Disease / metabolism
  • Female
  • Gene Expression
  • Humans
  • Male
  • Malondialdehyde / metabolism
  • Middle Aged
  • Oxidative Stress*
  • Precancerous Conditions / genetics
  • Precancerous Conditions / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • Transforming Growth Factor beta / genetics*


  • RNA, Messenger
  • RNA, Neoplasm
  • Transforming Growth Factor beta
  • Malondialdehyde