Original Article
Copyright ©2011 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Jan 14, 2011; 17(2): 181-190
Published online Jan 14, 2011. doi: 10.3748/wjg.v17.i2.181
LY294002 potentiates the anti-cancer effect of oxaliplatin for gastric cancer via death receptor pathway
Jie Liu, Xue-Qiong Fu, Wei Zhou, Hong-Gang Yu, Jie-Ping Yu, He-Sheng Luo
Jie Liu, Xue-Qiong Fu, Wei Zhou, Institute of Gastroenterology and Hepatology, Wuhan University Medical School, Wuhan 430060, Hubei Province, China
Hong-Gang Yu, Jie-Ping Yu, He-Sheng Luo, Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei Province, China
Author contributions: Liu J, Zhou W and Fu XQ performed the majority of experiments; Yu HG provided vital reagents and analytical tools and was also involved in editing the manuscript; Luo HS and Yu JP designed the study and provided financial support for this work; Liu J wrote the manuscript.
Supported by The National Natural Science Foundation of China, No. 30470782
Correspondence to: He-Sheng Luo, Professor, Department of Gastroenterology, Renmin Hospital of Wuhan University, 238 Jiefang Street, Wuhan 430060, Hubei Province, China. luotangwh@gmail.com
Telephone: +86-27-88042134 Fax: +86-27-88042292
Received: September 14, 2010
Revised: December 14, 2010
Accepted: December 21, 2010
Published online: January 14, 2011
Abstract

AIM: To examine the effects of combined treatment of oxaliplatin and phosphatidylinositol 3’-kinase inhibitor, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002) for gastric cancer.

METHODS: Cell viability was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Apoptotic cells were detected by flow cytometric analysis and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling assay. Western blotting and immuno-precipitation were used to examine protein expression and recruitment, respectively. Nuclear factor κB (NFκB) binding activities were investigated using electrophoretic mobility shift assay. Nude mice were used to investigate tumor growth.

RESULTS: Treatment with combined oxaliplatin and LY294002 resulted in increased cell growth inhibition and cell apoptosis in vitro, and increased tumor growth inhibition and cell death in the tumor mass in vivo. In MKN45 and AGS cells, oxaliplatin treatment promoted both protein kinase B (Akt) and NFκB activation, while pretreatment with LY294002 significantly attenuated oxaliplatin-induced Akt activity and NFκB binding. LY294002 promoted oxaliplatin-induced Fas ligand (FasL) expression, Fas-associated death domain protein recruitment, caspase-8, Bid, and caspase-3 activation, and the short form of cellular caspase-8/FLICE-inhibitory protein (c-FLIPS) inhibition. In vivo, LY294002 inhibited oxaliplatin-induced activation of Akt and NFκB, and increased oxaliplatin-induced expression of FasL, inhibition of c-FLIPS, and activation of caspase-8, Bid, and caspase-3.

CONCLUSION: Combination of oxaliplatin and LY294002 was therapeutically promising for gastric cancer treatment. The enhanced sensitivity of the combined treatment was associated with the activation of the death receptor pathway.

Keywords: Gastric cancer, Oxaliplatin, Phosphatidylinositol 3’-kinase/Akt pathway, Death receptor pathway, Apoptosis, LY294002