Gambogenic acid mediated apoptosis through the mitochondrial oxidative stress and inactivation of Akt signaling pathway in human nasopharyngeal carcinoma CNE-1 cells

Eur J Pharmacol. 2011 Feb 10;652(1-3):23-32. doi: 10.1016/j.ejphar.2010.11.018. Epub 2010 Nov 28.

Abstract

In the present study, Gambogenic acid exhibits potential anti-tumor activity in several cancer cell lines. However, Gambogenic acid-induced apoptosis mechanism is not well understood. Here, we report that Gambogenic acid was capable to induce CNE-1 cells apoptosis and caused mitochondrial and endoplasmic reticulum injury, analyzed via transmission electron microscopy and acridine orange/ethidium bromide (AO/EB) double staining. To quantitatively analyze apoptosis, through the propidium iodide (PI)/Annexin V-FITC double staining to detect cell apoptosis, PI staining of the cell cycle distribution. To further explore the potential mechanism of Gambogenic acid mediated apoptosis in CNE-1 cells, we also examined mitochondrial oxidative stress in the levels of reactive oxygen species, the release of cytochrome c, intracellular Ca(2+) concentration and mitochondrial membrane potential by flow cytometry. Moreover, Gambogenic acid could result in a time and concentration-dependent decrease in Phospho-Akt expression, basal expression levels of Akt change was not obvious, In addition, we detected Bcl-2 family including Bcl-2, Bax and Bad expression in mRNA level. This resulted in a decrease of Bcl-2 and Bad increased in CNE-1 cells after Gambogenic acid treatment. Overall, our results indicated that Gambogenic acid mediated apoptosis through inactivation of Akt, accompanied with mitochondrial oxidative stress and cross-talk with Bcl-2 family in the process of apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Carcinoma
  • Cell Proliferation / drug effects
  • Humans
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Nasopharyngeal Carcinoma
  • Nasopharyngeal Neoplasms / metabolism
  • Nasopharyngeal Neoplasms / pathology
  • Oncogene Protein v-akt / metabolism*
  • Oxidative Stress
  • Reactive Oxygen Species / metabolism*
  • Signal Transduction / drug effects
  • Terpenes / pharmacology*
  • Tumor Cells, Cultured
  • Xanthenes
  • Xanthones / pharmacology*
  • bcl-2-Associated X Protein / metabolism

Substances

  • Reactive Oxygen Species
  • Terpenes
  • Xanthenes
  • Xanthones
  • bcl-2-Associated X Protein
  • neo-gambogic acid
  • Oncogene Protein v-akt