| Literature DB >> 24280585 |
Yan-Cong Li1, Shu-Ming He2, Zhi-Xu He3, Minghua Li4, Yinxue Yang5, Jian-Xin Pang6, Xueji Zhang7, Kevin Chow4, Qingyu Zhou4, Wei Duan8, Zhi-Wei Zhou4, Tianxin Yang9, Gui-Hua Huang10, Aibing Liu11, Jia-Xuan Qiu12, Jun-Ping Liu13, Shu-Feng Zhou14.
Abstract
Plumbagin (PLB) has shown anti-cancer activity but the mechanism is unclear. This study has found that PLB has a potent pro-apoptotic and pro-autophagic effect on A549 and H23 cells. PLB arrests cells in G2/M phase, and increases the intracellular level of reactive oxygen species in both cell lines. PLB dose-dependently induces autophagy through inhibition of PI3K/Akt/mTOR pathway as indicated by reduced phosphorylation of Akt and mTOR. Inhibition or induction of autophagy enhances PLB-induced apoptosis. There is crosstalk between PLB-induced apoptosis and autophagy. These findings indicate that PLB initiates both apoptosis and autophagy in NSCLC cells through coordinated pathways.Entities:
Keywords: Apoptosis; Autophagy; Non-small-cell lung cancer; PI3K/Akt/mTOR; Plumbagin
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Year: 2013 PMID: 24280585 DOI: 10.1016/j.canlet.2013.11.001
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679