蛋白激酶B
紫杉醇
mTORC1型
细胞凋亡
PI3K/AKT/mTOR通路
癌症研究
卵巢癌
安普克
激酶
mTORC2型
活性氧
药理学
化学
细胞生物学
生物
医学
癌症
蛋白激酶A
内科学
生物化学
作者
Hui Sun,Yuee Teng,Jinchao Li
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2011-11-01
卷期号:310 (1): 118-128
被引量:70
标识
DOI:10.1016/j.canlet.2011.06.010
摘要
Here we report an oral alkylphospholipid perifosine dramatically sensitizes chemo-resistant ovarian cancer cells to paclitaxel induced cell death and apoptosis in vitro. We found that co-administration perifosine with paclitaxel in human ovarian cancer cells led to the inhibition of AKT/mTOR complex 1 (mTORC1), a marked increase in ceramide and reactive oxygen species (ROS) production, and a striking increase in the activation of pro-apoptosis pathways, including caspase 3, c-Jun N-terminal kinases (JNK) and AMP-activated protein kinase (AMPK). These signaling events together caused a marked increase of cancer cell apoptosis. Combining paclitaxel with perifosine may represent a novel anti-ovarian cancer strategy.
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