Preclinical and clinical evaluation of broccoli supplements as inducers of glutathione S-transferase activity

Clin Cancer Res. 1997 Jan;3(1):25-30.

Abstract

Previous studies suggest that cruciferous vegetables may provide protection against carcinogen exposure by inducing detoxification enzymes. ICR(Ha) mice were gavaged with broccoli tablets (1 g/kg), and colon tissues were collected after treatment. Glutathione S-transferase (GST) activity was assayed and peaked on days 1 and 2 after treatment, respectively (P = 0.03). Elevations in GST activity were attributed to the increased expression of mu and pi. These data supported a clinical assessment of broccoli supplements. Twenty-nine subjects at increased risk for colorectal cancer were randomized to group 1 (no cruciferous vegetables) or group 2 (broccoli supplements, 3 g/day) for 14 days. Blood samples and colon biopsies were obtained pre- and postintervention. No significant difference was observed between the GST activities of the control and broccoli supplementation groups posttreatment. Mean lymphocyte GST activity was 107% of baseline in the broccoli supplementation group (range, 79-158%) and 102% of baseline in the control group (range, 75-158 percent;). Correlation of the GST activities of blood lymphocytes and colon mucosa taken simultaneously suggested that the GST activity of blood lymphocytes may be used as a biomarker of the responsiveness of colon tissue to chemopreventive regimens. Future clinical studies evaluating cruciferous vegetables should consider using concentrated dietary supplements in subjects with a previous history of colorectal cancer.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Animals
  • Brassica*
  • Chemoprevention
  • Colorectal Neoplasms / enzymology
  • Colorectal Neoplasms / prevention & control
  • Dietary Supplements*
  • Enzyme Induction
  • Female
  • Gastric Mucosa / enzymology
  • Glutathione Transferase / biosynthesis*
  • Humans
  • Lymphocytes / enzymology
  • Male
  • Mice
  • Mice, Inbred ICR
  • Middle Aged
  • Risk Factors

Substances

  • Glutathione Transferase