Gamma-mangostin, a micronutrient of mangosteen fruit, induces apoptosis in human colon cancer cells

Molecules. 2012 Jul 3;17(7):8010-21. doi: 10.3390/molecules17078010.

Abstract

Recently colorectal cancer rates have increased rapidly in Taiwan. The treatment of colorectal cancer includes surgery, radiation therapy and chemotherapy. Mangosteen (Garcinia mangostana) is a famous Asian tropical fruit. γ-Mangostin is a xanthone derivative isolated from the fruit hull. In previous studies, we found evidence of anti-inflammatory and anti-brain tumor activities in γ-mangostin. In this study, we performed further studies to assess the apoptotic effects of γ-mangostin on colorectal adenocarcinoma cells HT29. γ-Mangostin showed concentration and time-dependent cytotoxic effects on HT29 cells. Microscopic observation under Giemsa staining showed that γ-mangostin induced cellular swelling and the appearance of apoptotic bodies, characteristic of apoptosis in HT29 cells. In addition, flow cytometry analysis showed an increase of hypodiploid cells in γ-mangostin-treated HT29 cells, while enhancement of intracellular peroxide production was detected in the same γ-mangostin-treated cells by DCHDA assay and DiOC6(3) staining. In view of the above results, γ-mangostin has demonstrated anticancer activity and induces apoptosis in HT29 colorectal adenocarcinoma cells. The evidence suggests that γ-mangostin could serve as a micronutrient for colon cancer prevention and is a potential lead compound for the development of anti-colon cancer agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Catalase / metabolism
  • Cell Proliferation / drug effects
  • Cell Shape / drug effects
  • Colonic Neoplasms / drug therapy
  • Colonic Neoplasms / pathology*
  • Diploidy
  • Drug Screening Assays, Antitumor
  • Fruit / chemistry*
  • Garcinia mangostana / chemistry*
  • HT29 Cells
  • Humans
  • Intracellular Space / drug effects
  • Intracellular Space / metabolism
  • Micronutrients / pharmacology*
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Mitochondrial Membranes / drug effects
  • Mitochondrial Membranes / metabolism
  • Peroxides / metabolism
  • Phytotherapy
  • Time Factors
  • Xanthones / chemistry
  • Xanthones / pharmacology*

Substances

  • Micronutrients
  • Peroxides
  • Xanthones
  • Catalase
  • mangostin