13-Oxyingenol dodecanoate, a cytotoxic ingenol derivative, induces mitochondrial apoptosis and caspase-dependent Akt decrease in K562 cells

被引:7
作者
Liu, Ming [1 ]
Zhang, Weiyi [1 ]
Wang, Genzhu [1 ]
Song, Xiaoping [1 ]
Zhao, Xingzeng [2 ]
Wang, Xiangyun [3 ]
Qi, Xin [1 ]
Li, Jing [1 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, Minist Educ, Key Lab Marine Drugs, Qingdao 266003, Peoples R China
[2] Jiangsu Prov & Chinese Acad Sci, Inst Bot, Nanjing Bot Garden Mem Sun Yat Sen, Nanjing 210014, Jiangsu, Peoples R China
[3] Nanjing Spring & Autumn Biol Engn Co Ltd, Nanjing 210014, Jiangsu, Peoples R China
关键词
13-Oxyingenol dodecanoate; Apoptosis; Euphorbia kansui; mTOR; Akt; CHRONIC MYELOID-LEUKEMIA; PROTEIN-KINASE-C; COLON-CANCER CELLS; ACTINIC KERATOSIS; BCR-ABL; INHIBITORS; MEBUTATE; PEP005; ACTIVATION; RESISTANCE;
D O I
10.1007/s13277-015-4495-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
13-Oxyingenol dodecanoate (13OD) is an ingenol derivative prepared from Chinese traditional medicine Euphorbia kansui without any report about its bioactivity. The present study demonstrated for the first time that 13OD displayed potent cytotoxicity against chronic myeloid leukemia K562 cells in vitro. 13OD inhibited proliferation, induced G2/M phase arrest, and exhibited potent apoptotic activity in K562 cells. In K562 cells, 13OD disrupted the mitochondrial membrane potential and induced high level of ROS, which played an indispensable role in 13OD-induced apoptosis. Further investigations on the molecular mechanisms revealed that total Akt protein level was decreased in a caspase-dependent way after treatment with 13OD; in addition, ERK was activated by 13OD, and this activation played a protective role in 13OD stimulation. Altogether, these results revealed that the cytotoxic ingenol derivative 13OD induced apoptosis with novel mechanisms for the proapoptotic function in cancer cells, and suggested that 13OD may serve as a lead template for rational drug design and for future anticancer agent development.
引用
收藏
页码:6227 / 6238
页数:12
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