Celastrus Orbiculatus Extract Potentiates the Sensitivity of Cisplatin Via Caspase-Depenent Apoptosis in Gastric Cancer

被引:16
|
作者
Wang, Weimin [1 ,2 ,3 ]
Zhou, Yan [1 ,2 ]
Yao, Qiang [2 ]
Liu, Weihua [2 ]
Xiang, Liangliang [1 ,3 ]
Ni, Tengyang [1 ,3 ]
Dai, Xiaojun [1 ,4 ]
Liu, Yanqing [1 ,2 ,3 ]
机构
[1] Yangzhou Univ, Med Coll, Inst Combining Chinese Tradit & Western Med, Yangzhou, Jiangsu, Peoples R China
[2] Yangzhou Univ, Yixing Hosp, Med Coll, Dept Oncol, Yixing, Jiangsu, Peoples R China
[3] Yangzhou Univ, Coll Med, State Adm Tradit Chinese Med, Key Lab Tox Pathogens Based Therapeut Approaches, Yangzhou, Jiangsu, Peoples R China
[4] Yangzhou Univ, Clin Coll Tradit Chinese Med, Dept Oncol, Yangzhou, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Celastrus Orbiculatus; cisplatin; gastric cancer; apoptosis; western blotting; CCK8; caspase pathway; TUMOR ANGIOGENESIS; SIGNALING PATHWAY; BREAST-CANCER; CHEMOTHERAPY; RESISTANCE; PROLIFERATION; ACTIVATION; PREVENTION; CARCINOMA; EFFICACY;
D O I
10.2174/1871520618666180911110124
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Cisplatin-based treatment often leads to therapeutic failure because the acquisition of cisplatin resistance. The combination of cisplatin with other agents has been recognized as a promising strategy to overcome cisplatin resistance. Objective: Celastrus orbiculatus is a traditional Chinese medicine from Celastraceae family with multiple pharmacological activities. We previously found that the ethyl acetate extract of Celastrus orbiculatus (COE) exhibited significant antitumor activity in gastric cancer. Here, we asked whether COE could increase the sensitivity of cisplatin. Methods: We use CCK8 assay to show synergistic cytotoxicity of COE and cisplatin. Then, PI single staining and FITC-Annexin V/PI double staining were used to observe apoptotic cells through flow cytometry. The proteins of caspase signaling pathway were examined by Western blotting. Results: COE and cisplatin showed synergistic cytotoxicity in a dose-dependent manner in BGC 823 and SGC 7901 gastric cancer cells, and COE could increase the number of apoptotic cells upon cisplatin treatment in vitro. Moreover, our results indicated that COE could enhance cisplatin induced activation of caspase-8 or caspase-9/caspase-3/PARP1 signaling pathways. The xenograft study further confirmed that COE increased the sensitivity of cisplatin in vivo. Conclusion: Our findings provided new evidence that COE could increase the sensitivity of cisplatin on the antitumor effect.
引用
收藏
页码:2206 / 2211
页数:6
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