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西红花苷通过抑制Akt/mTOR活性诱导肝癌细胞自噬性凋亡。

Crocin induces autophagic apoptosis in hepatocellular carcinoma by inhibiting Akt/mTOR activity.

作者信息

Yao Chong, Liu Bing-Bing, Qian Xiao-Dong, Li Li-Qin, Cao Heng-Bin, Guo Qiao-Sheng, Zhou Gui-Fen

机构信息

Institute of Chinese Medicinal Materials, Nanjing Agricultural University, Nanjing 210095, China.

Pharmaceutical Department, Huzhou Central Hospital, Huzhou 313003, China.

出版信息

Onco Targets Ther. 2018 Apr 9;11:2017-2028. doi: 10.2147/OTT.S154586. eCollection 2018.

Abstract

BACKGROUND

Autophagy induction is a common mechanism for antitumor chemicals in induction of cancer cell death. However, the role of autophagy in crocin-induced apoptosis is barely studied in hepatocellular carcinoma (HCC).

MATERIALS AND METHODS

The influence of crocin on growth, apoptosis, and autophagy and its mutual relations were analyzed by Cell Counting Kit-8 assay, flow cytometer, EGFP-LC3 puncta analysis, and Western blot in HCC cells. The activities of Akt/mTOR axis and its roles in autophagy regulation were also detected by Western blot in HCC cells treated with crocin. Finally, the roles of Akt/mTOR axis in crocin-induced autophagic apoptosis were analyzed by Western blot and flow cytometer in HCC cells.

RESULTS

The results showed that crocin can induce growth inhibition in a does- and time-dependent pattern by apoptosis. Increased LC3 puncta and upregulated LC3-II accumulation was observed as early as at 6 hours in HepG2 and HCCLM3 cells treated with 3 mg/mL crocin. Moreover, apoptosis analysis using flow cytometer and cleaved poly (ADP-ribose) polymerase detection revealed that autophagy initiation was prior to apoptosis activation in HCC cells treated with crocin. When autophagy was blocked with 3-methyladenine, crocin-induced apoptosis was inhibited in HCC cells. Furthermore, crocin treatment constrained the activities of key proteins in Akt/mTOR signaling, such as p-Akt (S473), p-mTOR (S2448), and p-p70S6K (T389), suggesting that crocin could induce autophagic apoptosis in HCC cells in an Akt/mTOR-dependent mechanism. Indeed, when autophagy was suppressed by forced expression of Akt, the crocin-induced apoptosis was also impaired in HCC cells.

CONCLUSION

The results suggested that crocin could induce autophagic apoptosis in HCC cells by inhibiting Akt/mTOR activity. This study originally revealed that autophagic apoptosis is a novel cytotoxic function of crocin, which lays the theoretical foundation for clinical application of crocin in HCC.

摘要

背景

自噬诱导是抗肿瘤化学物质诱导癌细胞死亡的常见机制。然而,在肝细胞癌(HCC)中,藏红花素诱导的凋亡过程中自噬的作用鲜有研究。

材料与方法

采用细胞计数试剂盒-8法、流式细胞仪、EGFP-LC3斑点分析和蛋白质免疫印迹法,分析藏红花素对肝癌细胞生长、凋亡和自噬的影响及其相互关系。同时,采用蛋白质免疫印迹法检测Akt/mTOR轴的活性及其在自噬调节中的作用。最后,通过蛋白质免疫印迹法和流式细胞仪分析Akt/mTOR轴在藏红花素诱导的自噬性凋亡中的作用。

结果

结果表明,藏红花素可通过凋亡以剂量和时间依赖性方式诱导生长抑制。在用3mg/mL藏红花素处理的HepG2和HCCLM3细胞中,早在6小时就观察到LC3斑点增加和LC3-II积累上调。此外,流式细胞仪凋亡分析和裂解的聚(ADP-核糖)聚合酶检测显示,在用藏红花素处理的肝癌细胞中,自噬启动先于凋亡激活。当用3-甲基腺嘌呤阻断自噬时,藏红花素诱导的凋亡在肝癌细胞中受到抑制。此外,藏红花素处理抑制了Akt/mTOR信号通路中关键蛋白如p-Akt(S473)、p-mTOR(S2448)和p-p70S6K(T389)的活性,表明藏红花素可通过Akt/mTOR依赖性机制诱导肝癌细胞发生自噬性凋亡。事实上,当通过强制表达Akt抑制自噬时,藏红花素诱导的凋亡在肝癌细胞中也受到损害。

结论

结果表明,藏红花素可通过抑制Akt/mTOR活性诱导肝癌细胞发生自噬性凋亡。本研究首次揭示自噬性凋亡是藏红花素的一种新的细胞毒性功能,为藏红花素在肝癌临床应用中奠定了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a72e/5898595/d8f0c3f79d20/ott-11-2017Fig1.jpg

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