ROS-mediated autophagy induced by dysregulation of lipid metabolism plays a protective role in colorectal cancer cells treated with gambogic acid.

Abstract

Gambogic acid (GA), the main active component of gamboge resin, has potent antitumor activity both in vivo and in vitro. However, the underlying molecular mechanisms remain unclear. In this study, we found that GA could initiate autophagy in colorectal cancer cells, and inhibition of the autophagy process accelerated the effect of proliferative inhibition and apoptotic cell death induced by GA, implying a protective role of autophagy. Two-dimensional electrophoresis-based proteomics showed that GA treatment altered the expression of multiple proteins involved in redox signaling and lipid metabolism. Functional studies revealed that GA-induced dysregulation of lipid metabolism could activate 5-lipoxygenase (5-LOX), resulting in intracellular ROS accumulation, followed by inhibition of Akt-mTOR signaling and autophagy initiation. Finally, results using a xenograft model suggested ROS-induced autophagy protect against the antitumor effect of GA. Taken together, these data showed new biological activities of GA against colorectal cancer underlying the protective role of ROS-induced autophagy. This study will provide valuable insights for future studies regarding the anticancer mechanisms of GA.

• Authors: Haiyuan Zhang, Yunlong Lei, Ping Yuan, Lingjun Li, Chao Luo, Rui Gao, Jun Tian, Zuohua Feng, Edouard C Nice, Jun Sun
• Journal: PloS one (PLoS One) Vol. 9 Issue 5 Pg. e96418 ( 2014) ISSN: 1932-6203 [Electronic] United States
• PMID: 24810758 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• Reactive Oxygen Species
• Xanthones
• gambogic acid

Topics

• Antineoplastic Agents (pharmacology, therapeutic use)
• Apoptosis (drug effects)
• Autophagy (drug effects, physiology)
• Cell Line, Tumor
• Colorectal Neoplasms (drug therapy, metabolism)
• Humans
• Lipid Metabolism (drug effects, physiology)
• Reactive Oxygen Species (metabolism)
• Signal Transduction (drug effects)
• Xanthones (pharmacology, therapeutic use)