Autophagy inhibition promotes paclitaxel-induced apoptosis in cancer cells |
| |
Authors: | Xi Guangmin Hu Xiaoyan Wu Baolin Jiang Hanming Young Charles Y F Pang Yingxin Yuan Huiqing |
| |
Affiliation: | Department of Biochemistry and Molecular Biology, Shandong University School of Medicine, Jinan, China. |
| |
Abstract: | Paclitaxel has been demonstrated to be an effective mitotic inhibitor and apoptosis inducer to treat aggressive malignancies. In this paper, we have provided a line of evidence that promotion of apoptotic cell death by paclitaxel was accompanied with induction of autophagy in A549 cells. Paclitaxel treatment could lead to the formation of acidic vesicular organelles (AVOs), the induction of Atg5, Beclin 1 and microtubule-associated protein 1 light chain 3 (LC3) expressions, and the increase of punctate fluorescent signals in A549 cells pre-transfected with green fluorescent protein (GFP)-tagged LC3. Interestingly, paclitaxel-mediated apoptotic cell death was further potentiated by pretreatment with autophagy inhibitor 3-methyladenine (3-MA) or small interfering RNA against the autophagic gene beclin1. These findings suggest that paclitaxel-elicited autophagic response plays a protective role that impedes the eventual cell death, and inhibition of autophagy could be an adjunctive strategy for enhancing chemotherapeutic effect of paclitaxel as an antitumor agent. |
| |
Keywords: | AVOs, acidic vesicular organelles LC3, microtubule-associated protein 1 light chain 3 3-MA, 3-methyladenine MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazoliumbromide |
本文献已被 ScienceDirect PubMed 等数据库收录! |
|