Chemopreventive effects of Ginkgo biloba extract in estrogen-negative human breast cancer cells

Arch Pharm Res. 2013 Jan;36(1):102-8. doi: 10.1007/s12272-013-0002-0.

Abstract

Excessive level of estrogen is considered as a main cause of breast cancer, therefore, many studies have focused on estrogen receptor (ER)-positive breast cancer, even though ER-negative cancer has a poor prognosis than ER-positive breast cancer. We evaluated the anti-cancer effects of Ginkgo biloba extract (GBE) in estrogen-independent breast cancer. GBE has been traditionally used as a platelet activating factor, a circulatory stimulant, a tonic, and anti-asthmatic drug, and anti-cancer agent. However, anti-cancer effects of GBE on ER-negative breast cancer have not been proved yet. In this study, we tested chemotherapeutic potential of GBE in the MDA-MB-231 (ER-negative) human breast cancer cell line. Our results showed that cytotoxicity effects of GBE in MDA-MB-231 lead to DNA fragmentation at high concentrations (500 and 1,000 μg/ml). Caspase-3 was significantly activated and mRNA levels of apoptosis-related genes (Bcl-2 and Bax) were altered. These results indicate that GBE induces apoptosis in MDA-MB-231 cells. It is presumed that GBE has chemopreventive effects in ER-independent breast cancer through anti-proliferation and apoptosis-inducing activities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anticarcinogenic Agents / isolation & purification
  • Anticarcinogenic Agents / pharmacology*
  • Apoptosis / drug effects
  • Apoptosis Regulatory Proteins / biosynthesis
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Breast Neoplasms / prevention & control*
  • Caspase 3 / metabolism
  • Cell Culture Techniques
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Chromatography, High Pressure Liquid
  • DNA Fragmentation / drug effects
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • Estrogens / metabolism*
  • Female
  • Ginkgo biloba / chemistry*
  • Humans
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology*
  • Real-Time Polymerase Chain Reaction

Substances

  • Anticarcinogenic Agents
  • Apoptosis Regulatory Proteins
  • Estrogens
  • Plant Extracts
  • Caspase 3