Yao Chong, Liu Bing-Bing, Qian Xiao-Dong, Li Li-Qin, Cao Heng-Bin, Guo Qiao-Sheng, Zhou Gui-Fen
Institute of Chinese Medicinal Materials, Nanjing Agricultural University, Nanjing 210095, China.
Pharmaceutical Department, Huzhou Central Hospital, Huzhou 313003, China.
Onco Targets Ther. 2018 Apr 9;11:2017-2028. doi: 10.2147/OTT.S154586. eCollection 2018.
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).
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.
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.
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.
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。
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。