Cannabinoid Receptor Agonist as an Alternative Drug in 5-Fluorouracil-resistant Gastric Cancer Cells

被引:0
|
作者
Xian, Xiang-Shu [1 ,2 ]
Park, Hyeyeon [1 ]
Choi, Myung-Gyu [1 ]
Park, Jae Myung [1 ]
机构
[1] Catholic Univ Korea, Div Gastroenterol, Dept Internal Med, Coll Med, Seoul 137070, South Korea
[2] Yantai Yuhuangding Hosp, Dept Internal Med, Div Gastroenterol, Yantai, Shandong, Peoples R China
关键词
Gastric cancer; cannabinoids; fluorouracil; drug resistance; apoptosis; CERAMIDE ACCUMULATION; MEDIATED APOPTOSIS; R(+)-METHANANDAMIDE; CHEMOTHERAPY; ACTIVATION; CARCINOMA; PROSTATE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fluorouracil is the main chemotherapeutic drug used for gastrointestinal cancers, which suffers the important problem of treatment resistance. There is little information whether cannabinoid agonists can be used as an alternative drug for fluorouracil-resistant gastric cancer cells. In this study, we investigated the effects of a cannabinoid agonist, WIN-55,212-2, on 5-fluorouracil (5-FU)-resistant human gastric cancer cells, to examine whether the cannabinoid agonist may be an alternative therapy. Survival of the 5-FU-resistant gastric cancer cell line, SNU-620-5FU/1000, was not significantly reduced even by a high dose of 5-FU treatment. However, WIN-55,212-2 inhibited the proliferation of SNU-620-5FU/1000 and enhanced their apoptosis, as indicated by an increase of apoptotic cell proportion, activated caspase-3 and Poly (ADP-ribose) polymerase cleavage. Furthermore, WIN-55,212-2 reduced phospho-extracellular-signal-regulated kinases (ERK) 1/2, phospho-Akt (protein kinase B), B-cell lymphoma-2 (BCL2) and BCL2-associated X (BAX) protein expression in 5-FU-resistant gastric cancer cells. These results indicate that a cannabinoid agonist may, indeed, be an alternative chemotherapeutic agent for 5-FU-resistant gastric cancer.
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页码:2541 / 2547
页数:7
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