Autophagy Induction by Trichodermic Acid Attenuates Endoplasmic Reticulum Stress-Mediated Apoptosis in Colon Cancer Cells

被引:12
作者
Qu, Junyan [1 ]
Zeng, Cheng [1 ]
Zou, Tingting [1 ]
Chen, Xu [1 ]
Yang, Xiaolong [2 ]
Lin, Zhenghong [1 ]
机构
[1] Chongqing Univ, Sch Life Sci, Chongqing 401331, Peoples R China
[2] South Cent Univ Nationalities, Sch Pharmaceut Sci, Modernizat Engn Technol Res Ctr Ethn Minor Med Hu, Wuhan 430074, Peoples R China
基金
中央高校基本科研业务费专项资金资助; 中国国家自然科学基金;
关键词
TDA; ER stress; apoptosis; autophagy; colorectal cancer; UNFOLDED PROTEIN RESPONSE; COLORECTAL-CANCER; ER-STRESS; M-COPA; GOLGI SYSTEM; DEATH; TUMOR; ACTIVATION; PATHWAY; THAPSIGARGIN;
D O I
10.3390/ijms22115566
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal cancer (CRC) is the third leading malignant tumor in the world, which has high morbidity and mortality. In this study we found that trichodermic acid (TDA), a secondary metabolite isolated from the plant endophytic fungus Penicillium ochrochloronthe with a variety of biological and pharmacological activities, exhibited the antitumor effects on colorectal cancer cells in vitro and in vivo. Our results showed that TDA inhibited the proliferation of colon cancer cells in a dose-dependent manner. TDA induces sustained endoplasmic reticulum stress, which triggers apoptosis through IRE1 alpha/XBP1 and PERK/ATF4/CHOP pathways. In addition, we found that TDA mediated endoplasmic reticulum stress also induces autophagy as a protective mechanism. Moreover, combined treatment of TDA with autophagy inhibitors significantly enhanced its anticancer effect. In conclusion, our results indicated that TDA can induce ER stress and autophagy mediated apoptosis, suggesting that targeting ER stress and autophagy may be an effective strategy for the treatment of CRC.
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页数:19
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