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姜黄素通过抑制 PI3K/Akt/mTOR 通路调节人肺癌 A549 细胞凋亡和自噬的抗肿瘤活性。

Antitumor activity of curcumin by modulation of apoptosis and autophagy in human lung cancer A549 cells through inhibiting PI3K/Akt/mTOR pathway.

机构信息

School of Public Health, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi 710061, P.R. China.

Department of Nuclear Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.

出版信息

Oncol Rep. 2018 Mar;39(3):1523-1531. doi: 10.3892/or.2018.6188. Epub 2018 Jan 4.

Abstract

Curcumin is known to exhibit anticancer effects on various cancers with selective cytotoxicity in tumor cells. In the present study, the effects of curcumin‑induced multiple PCDs on human non‑small cell lung cancer (NSCLC) cells and the potential molecular mechanisms of apoptosis and autophagy triggered by curcumin via the PI3K/Akt/mTOR signaling pathway were explored, further confirmed by co‑culture of curcumin with mTOR blocker rapamycin and PI3K/Akt inhibitor LY294002. The anti‑proliferation effect of different stimulus was measured by MTT assay. Apoptosis was detected by flow cytometry. Autophagy induction was detected by MDC labeling and western blotting of Beclin1, LC3, and p62 expression. The mRNA and protein expression levels of Akt and mTOR were assayed by real‑time fluorescence quantitative (qRT‑PCR) technique and western blotting. Our results showed that curcumin inhibited the viability of A549 cells time‑ and dose‑dependently. In addition, a dosage-dependent A549 cell apoptosis‑induction phenomena was observed by the curcumin intervention. Moreover, obvious autophagy was induced after curcumin‑treatment, characterized by the formation of fluorescent particles [autophagic vesicles (AVs)] and significant increase in ratio of LC3‑Ⅱ/LC3‑Ⅰ and Beclin1 as well as decreased p62 expression. Furthermore, the effect of curcumin on a substantial downregulation of phosphatidylinositol 3‑kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) pathway was observed. It is worth noting that the inhibition of mTOR by rapamycin or of PI3K/Akt by LY294002 augmented curcumin‑induced apoptosis and autophagy, leading to significant inhibition of cell proliferation. From these findings, it can be speculated that curcumin potently inhibit the cell growth of NSCLC A549 cells through inducing both apoptosis and autophagy by inhibition of the PI3K/Akt/mTOR pathway. These results support the potential use of curcumin as a novel candidate in treatment of human lung cancer.

摘要

姜黄素对多种癌症具有抗癌作用,并对肿瘤细胞具有选择性细胞毒性。本研究探讨了姜黄素诱导的多种细胞程序性死亡(PCD)对人非小细胞肺癌(NSCLC)细胞的影响,以及通过 PI3K/Akt/mTOR 信号通路诱导细胞凋亡和自噬的潜在分子机制,并通过与 mTOR 抑制剂雷帕霉素和 PI3K/Akt 抑制剂 LY294002 共培养进一步证实。采用 MTT 法测定不同刺激物的抗增殖作用。通过流式细胞术检测细胞凋亡。通过 MDC 标记和 Beclin1、LC3 和 p62 表达的 Western blot 检测自噬诱导。采用实时荧光定量(qRT-PCR)技术和 Western blot 法检测 Akt 和 mTOR 的 mRNA 和蛋白表达水平。结果表明,姜黄素呈时间和剂量依赖性抑制 A549 细胞活力。此外,姜黄素干预后观察到 A549 细胞凋亡诱导呈剂量依赖性。此外,姜黄素处理后明显诱导自噬,表现为形成荧光颗粒[自噬小体(AVs)],LC3-Ⅱ/LC3-Ⅰ比值和 Beclin1 显著增加,p62 表达减少。此外,还观察到姜黄素对磷脂酰肌醇 3-激酶(PI3K)/Akt/哺乳动物雷帕霉素靶蛋白(mTOR)通路的显著下调作用。值得注意的是,雷帕霉素抑制 mTOR 或 LY294002 抑制 PI3K/Akt 可增强姜黄素诱导的细胞凋亡和自噬,从而显著抑制细胞增殖。从这些发现可以推测,姜黄素通过抑制 PI3K/Akt/mTOR 通路诱导细胞凋亡和自噬,有力地抑制 NSCLC A549 细胞的生长。这些结果支持姜黄素作为一种新型候选药物用于治疗人类肺癌的潜力。

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