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

Margie L. Clapper, Christine E. Szarka, Gordon R. Pfeiffer, Todd A. Graham, Andrew M. Balshem, Samuel Litwin, Eric B. Goosenberg, Harold Frucht, Paul F. Engstrom

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

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 μ and π. 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 post-intervention. 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%). 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.

Original languageEnglish
Pages (from-to)25-30
Number of pages6
JournalClinical Cancer Research
Volume3
Issue number1
StatePublished - 1997

Keywords

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

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