Timosaponin AIII, a steroidal saponin, exhibits anti-tumor effect on taxol-resistant cells in vitro and in vivo

被引:28
|
作者
Song, Xiao-Yu [1 ,2 ]
Han, Feng-Ying [1 ,2 ]
Chen, Jing-Jie [1 ,2 ]
Wang, Wei [1 ,2 ]
Zhang, Yan [1 ,2 ]
Yao, Guo-Dong [1 ,2 ]
Song, Shao-Jiang [1 ,2 ]
机构
[1] Shenyang Pharmaceut Univ, Dept Nat Prod Chem, Shenyang 110016, Liaoning, Peoples R China
[2] Key Lab Computat Chem Based Nat Antitumor Drug Re, Shenyang, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Timosaponin AIII; Anemarrhena asphodeloides; Taxol-resistant cells; Apoptosis; MULTIDRUG-RESISTANCE; APOPTOSIS; RAS/RAF/MEK/ERK; ACTIVATION; AUTOPHAGY; MUTATIONS;
D O I
10.1016/j.steroids.2019.03.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Timosaponin AIII (TAIII), a steroidal saponin isolated from the rhizome of Anenuorhena asphodeloides, exerted cytotoxic effect in many cancer cell lines. However, the effect of TAIII on resistant tumor cancer cells was unclear. In this study, MTT assay showed that TAIII exhibited significant cytotoxicity against A549/Taxol and A2780/Taxol cells in vitro. Annexin V-FITC/PI staining revealed that TAIII induced apoptosis in A549/T and A2780/T cells. Furthermore, Western blot analysis demonstrated that TAIII inhibited the expressions of phosphatidylinositol 3-kinase (PI3K), protein kinase B (AKT), mammalian target of rapamycin (mTOR) as well as Ras, Raf, mitogen-activated protein kinase (MEPK), extracellular regulated protein kinases (ERK) in two taxol-resistant cancer cell lines. Besides, in vivo studies demonstrated that TAIII inhibited tumor growth in a nude mouse xenograft model. Additionally, TAIII (2.5 and 5 mg/kg) also down-regulated the protein expressions of PI3K/AKT/mTOR and Ras/Raf/MEK/ERK pathways in vivo. Taken together, these findings demonstrated that TAIII exhibited significant anti-tumor effect on taxol-resistant cells.
引用
收藏
页码:57 / 64
页数:8
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