Anthocyanin-rich extracts inhibit multiple biomarkers of colon cancer in rats

Geeta Lala1, Minnie Malik, Cuiwei Zhao

  • 1Department of Nutrition and Food Science, University of Maryland, College Park 20742, USA.

Nutrition and Cancer
|June 28, 2006
PubMed

Insights

Anthocyanin-rich extracts from bilberry, chokeberry, and grape show chemoprotective effects against colon cancer in rats by reducing aberrant crypt foci and cell proliferation. These extracts also influence gene expression and gut parameters, indicating multiple protective mechanisms.

Area of Science:

  • Nutritional biochemistry
  • Cancer chemoprevention
  • Pharmacology

Background:

  • Colon cancer is a significant health concern.
  • Dietary compounds, like anthocyanins, show potential for cancer prevention.
  • Anthocyanin-rich extracts (AREs) from bilberry, chokeberry, and grape warrant investigation for chemoprotective properties.

Purpose of the Study:

  • To investigate the chemoprotective activity of AREs from bilberry, chokeberry, and grape against colon cancer.
  • To assess the effects of AREs on multiple biomarkers of colon carcinogenesis in a rat model.
  • To evaluate the bioavailability of anthocyanins in serum, urine, and feces.

Main Methods:

  • Fischer 344 male rats were fed diets supplemented with AREs or a control diet for 14 weeks.
  • Evaluated biomarkers included colonic aberrant crypt foci (ACF), cell proliferation, oxidative DNA damage, and cyclooxygenase (COX) gene expression.
  • Anthocyanin levels in serum, urine, and feces were measured to assess bioavailability.

Main Results:

  • AREs from bilberry, chokeberry, and grape significantly reduced total ACF.
  • Bilberry and chokeberry AREs decreased the number of large ACF and colonic cell proliferation.
  • AREs modulated COX-2 mRNA expression, increased fecal anthocyanins, and reduced fecal bile acids.

Conclusions:

  • AREs from bilberry, chokeberry, and grape demonstrate chemoprotective effects against colon carcinogenesis in rats.
  • These extracts act through multiple mechanisms, including reducing aberrant crypt foci and modulating gene expression.
  • The findings support the potential of AREs as a dietary strategy for colon cancer prevention.