Aloe gel glucomannan induced colon cancer cell death via mitochondrial damage-driven PINK1/Parkin mitophagy pathway

被引:22
|
作者
Zhang, Ke [1 ]
Zhang, Duoduo [1 ]
Wang, Junqiao [1 ]
Wang, Yuting [1 ]
Hu, Jiarui [1 ]
Zhou, Yujia [1 ]
Zhou, Xingtao [1 ]
Nie, Shaoping [1 ]
Xie, Mingyong [1 ]
机构
[1] Nanchang Univ, State Key Lab Food Sci & Technol, China Canada Joint Lab Food Sci & Technol Nanchang, Key Lab Bioact Polysaccharides Jiangxi Prov, Nanchang, Peoples R China
基金
中国国家自然科学基金;
关键词
Aloe gel glucomannan; colon cancer; Mitophagy; ROS; TFEB; POLYSACCHARIDE; DYSFUNCTION; ACTIVATION; INJURY;
D O I
10.1016/j.carbpol.2022.119841
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Mitophagy can selectively remove damaged mitochondria, which is critical in regulating mitochondrial homeostasis in diseases, such as cancer. Herein, we found that Aloe gel glucomannan (AGP) significantly inhibited the proliferation of colon cancer cells. RNA-seq analysis revealed that AGP upregulated autophagy, lysosome and mitochondrial fission signal pathways in colon cancer cell line CT26. Notably, AGP induced the accumulation of impaired and reactive oxygen species (ROS)-generating mitochondria, which triggered excessive mitophagy. Interestingly, the mitophagy activator enhanced AGP-induced mitophagy and cytotoxicity, whereas the mitophagy inhibitor reversed the influence of AGP. Furthermore, activation of PINK1/Parkin mitophagy pathway and transcription factor EB (TFEB) signaling was dependent on ROS overproduction. Taken together, these results indicated that AGP induced cytotoxic mitophagy through ROS-related PINK1/Parkin pathway and TFEB activation in CT26 cells. The research would provide theoretical basis for the development of AGP as a promising anticancer agent.
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页数:12
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