Minnelide reduces tumor burden in preclinical models of osteosarcoma

被引:54
作者
Banerjee, Sulagna [1 ]
Thayanithy, Venugopal [1 ]
Sangwan, Veena [1 ]
Mackenzie, Tiffany N. [1 ]
Saluja, Ashok K. [1 ,2 ]
Subramanian, Subbaya [1 ,2 ]
机构
[1] Univ Minnesota, Dept Surg, Div Basic & Translat Res, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Masonic Canc Ctr, Minneapolis, MN 55455 USA
关键词
Triptolide; Minnelide; Osteosarcoma; Heat shock proteins; NF-kappa B; NF-KAPPA-B; HEAT-SHOCK PROTEINS; GLUCOCORTICOID-RECEPTOR; GENE-EXPRESSION; CELL-DEATH; IN-VITRO; TRIPTOLIDE; CANCER; ACTIVATION; APOPTOSIS;
D O I
10.1016/j.canlet.2013.02.050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is the most common bone cancer in children and adolescents with a 5-year survival rate of about 70%. In this study, we have evaluated the preclinical therapeutic efficacy of the novel synthetic drug, Minnelide, a prodrug of triptolide on osteosarcoma. Triptolide was effective in significantly inducing apoptosis in all osteosarcoma cell lines tested but had no significant effect on the human osteoblast cells. Notably, Minnelide treatment significantly reduced tumor burden and lung metastasis in the orthotopic and lung colonization models. Triptolide/Minnelide effectively downregulated the levels of pro-survival proteins such as heat shock proteins, cMYC, survivin and targets the NF-kappa B pathway. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:412 / 420
页数:9
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