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培非司亭与紫杉醇联合应用协同诱导卵巢癌细胞凋亡:不仅仅是 AKT 抑制。

Co-administration of perifosine with paclitaxel synergistically induces apoptosis in ovarian cancer cells: more than just AKT inhibition.

机构信息

Central Lab., Jining First People's Hospital, 6 Jiankang Road, Jining City, Shandong Province 272111, PR China.

出版信息

Cancer Lett. 2011 Nov 1;310(1):118-28. doi: 10.1016/j.canlet.2011.06.010. Epub 2011 Jun 29.

Abstract

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.

摘要

在这里,我们报告了一种口服烷基磷酸脂质 perifosine,它可显著增强化疗耐药的卵巢癌细胞对紫杉醇诱导的细胞死亡和凋亡的敏感性。我们发现,perifosine 与紫杉醇联合应用于人类卵巢癌细胞中,可抑制 AKT/mTOR 复合物 1(mTORC1),显著增加神经酰胺和活性氧(ROS)的产生,并显著增加促凋亡途径的激活,包括 caspase 3、c-Jun N-末端激酶(JNK)和 AMP 激活蛋白激酶(AMPK)。这些信号事件共同导致癌细胞凋亡的显著增加。紫杉醇与 perifosine 联合应用可能代表一种新的抗卵巢癌策略。

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