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

被引:48
作者
Yao, Chong [1 ,2 ]
Liu, Bing-Bing [3 ]
Qian, Xiao-Dong [2 ]
Li, Li-Qin [4 ]
Cao, Heng-Bin [2 ]
Guo, Qiao-Sheng [1 ]
Zhou, Gui-Fen [5 ]
机构
[1] Nanjing Agr Univ, Inst Chinese Med Mat, 1 Weigang, Nanjing 210095, Jiangsu, Peoples R China
[2] Huzhou Cent Hosp, Pharmaceut Dept, Huzhou 313003, Peoples R China
[3] TCM Hosp Changxin, Pharmaceut Dept, Huzhou 313100, Peoples R China
[4] Huzhou Cent Hosp, Huzhou Key Lab Mol Med, Huzhou 313000, Peoples R China
[5] Zhejiang Chinese Med Univ, Coll Pharmaceut Sci, Hangzhou 310053, Zhejiang, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2018年 / 11卷
基金
中国国家自然科学基金;
关键词
crocin; apoptosis; autophagy; Akt/mTOR; autophagic apoptosis; SAFFRON; DEGRADATION; MECHANISMS; HUNTINGTIN; INDUCTION; DEATH; CELLS; DRUG;
D O I
10.2147/OTT.S154586
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:2017 / 2028
页数:12
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