Triterpenoid saponin flaccidoside II from Anemone flaccida triggers apoptosis of NFI-associated malignant peripheral nerve sheath tumors via the MAPK-HO-I pathway

被引:7
作者
Han, Lin-tao [1 ]
Fang, Yin [1 ]
Cao, Yan [2 ]
Wu, Feng-hua [1 ]
Liu, E. [2 ]
Mo, Guo-yan [2 ]
Huang, Fang [1 ]
机构
[1] Minist Educ, China Key Lab TCM Resource & Prescript, Wuhan 430065, Hubei, Peoples R China
[2] Hubei Univ Chinese Med, Dept Pharm, 1 Tan Hua Lin Rd, Wuhan 430065, Hubei, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2016年 / 9卷
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
flaccidoside II; malignant peripheral nerve sheath tumors; apoptosis; MAPK; HO-1; HEME OXYGENASE-1; ENDOTHELIAL-CELLS; SIGNALING PATHWAY; NEUROFIBROMATOSIS TYPE-1; OLEANANE SAPONINS; GENE-EXPRESSION; UP-REGULATION; NITRIC-OXIDE; ACTIVATION; TARGET;
D O I
10.2147/OTT.S95597
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Malignant peripheral nerve sheath tumors (MPNSTs) are highly aggressive soft tissue neoplasms that are extremely rare and are frequently associated with neurofibromatosis type 1 patients. MPNSTs are typically fatal, and there is no effective treatment so far. In our previous study, we showed that flaccidoside II, one of the triterpenoid saponins isolated from Anemone flaccida Fr. Schmidt, has antitumor potential by inducing apoptosis. In the present study, we found that flaccidoside II inhibits proliferation and facilitates apoptosis in MPNST cell lines ST88-14 and S462. Furthermore, this study provides a mechanism by which the downregulation of heme oxygenase-1 via extracellular signal-regulated kinase-1/2 and p38 mitogen-activated protein kinase pathways is involved in the apoptotic role of flaccidoside II. This study suggested the potential of flaccidoside II as a novel pharmacotherapeutic approach for MPNSTs.
引用
收藏
页码:1969 / 1979
页数:11
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