蛋白激酶B
PI3K/AKT/mTOR通路
MAPK/ERK通路
体内
化学
激酶
MTT法
蛋白激酶A
膜联蛋白
A549电池
分子生物学
皂甙
细胞凋亡
细胞生长
癌细胞
体外
生物
生物化学
癌症
医学
遗传学
替代医学
生物技术
病理
作者
Xiaoyu Song,Han Feng-ying,Jingjie Chen,Wei Wang,Yan Zhang,Guo‐Dong Yao,Shao‐Jiang Song
出处
期刊:Steroids
[Elsevier BV]
日期:2019-04-02
卷期号:146: 57-64
被引量:43
标识
DOI:10.1016/j.steroids.2019.03.009
摘要
Timosaponin AIII (TAIII), a steroidal saponin isolated from the rhizome of Anemarrhena 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.
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