Chemopreventive effect of quercetin, a natural dietary flavonoid on prostate cancer in in vivo model

Clin Nutr. 2014 Aug;33(4):718-26. doi: 10.1016/j.clnu.2013.08.011. Epub 2013 Sep 3.

Abstract

Background & aim: Prostate cancer is one of the frequently diagnosed cancers in men. Increased Growth factor IGF-1/IGF-1R axis activation mediated by both PI3K/Akt or RAF/MEK/ERK system and AR expression remains important in the development and progression of prostate cancer. Targeting such system by dietary agents quercetin in vivo model could aid its application in both treatment as well as prevention of prostate cancer.

Methods: In our study the rats were divided into four groups; Group I: control (propylene glycol-vehicle), Group II: cancer-induced (MNU and Testosterone treated) rats, Group III: cancer-induced + Quercetin (200 mg/kg body wt/orally) and Group IV: Quercetin (200 mg/kg body wt) thrice a week. After the treatment period rats were sacrificed and the ventral and dorsolateral prostate lobes were dissected.

Results: Antioxidant enzymes and apoptotic proteins were significantly decreased in cancer-induced animal and upon quercetin supplement its level was increased. The IGFIR, AKT, AR, cell proliferative and anti-apoptotic proteins were increased in cancer-induced group whereas supplement of quercetin decreased its expression.

Conclusions: Quercetin down regulates the cell survival, proliferative and anti-apoptotic proteins thereby prevents prostate cancer, by acting as a chemopreventive agent in preclinical model.

Keywords: Antioxidant enzymes; Apoptosis; Cell survival; Proliferation; Prostate cancer; Quercetin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticarcinogenic Agents / pharmacology*
  • Antioxidants / pharmacology
  • Apoptosis / drug effects
  • CDC2 Protein Kinase
  • Caspase 3 / genetics
  • Caspase 3 / metabolism
  • Caspase 8 / genetics
  • Caspase 8 / metabolism
  • Caspase 9 / genetics
  • Caspase 9 / metabolism
  • Cell Cycle Checkpoints / drug effects
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cyclin-Dependent Kinases / genetics
  • Cyclin-Dependent Kinases / metabolism
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • Polyphenols / pharmacology*
  • Prostatic Neoplasms / drug therapy
  • Prostatic Neoplasms / prevention & control*
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Quercetin / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • bcl-2-Associated X Protein / genetics
  • bcl-2-Associated X Protein / metabolism

Substances

  • Anticarcinogenic Agents
  • Antioxidants
  • Bax protein, rat
  • Polyphenols
  • bcl-2-Associated X Protein
  • insulin-like growth factor-1, rat
  • Insulin-Like Growth Factor I
  • Quercetin
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • CDC2 Protein Kinase
  • Cdk1 protein, rat
  • Cyclin-Dependent Kinases
  • Casp3 protein, rat
  • Casp8 protein, rat
  • Casp9 protein, rat
  • Caspase 3
  • Caspase 8
  • Caspase 9