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溶酶体介导线粒体自噬促进茶多糖诱导的结肠癌细胞死亡通过 mTOR-TFEB 信号通路。

Lysosome-Mediated Cytotoxic Autophagy Contributes to Tea Polysaccharide-Induced Colon Cancer Cell Death via mTOR-TFEB Signaling.

机构信息

State Key Laboratory of Food Science and Technology, China-Canada Joint Lab of Food Science and Technology (Nanchang), Nanchang University, 235 Nanjing East Road, Nanchang, Jiangxi 330047, China.

出版信息

J Agric Food Chem. 2021 Jan 20;69(2):686-697. doi: 10.1021/acs.jafc.0c07166. Epub 2020 Dec 28.

Abstract

Targeting autophagy and lysosome may serve as a promising strategy for cancer therapy. Tea polysaccharide (TP) has shown promising antitumor effects. However, its mechanism remains elusive. Here, TP was found to have a significant inhibitory effect on the proliferation of colon cancer line HCT116 cells. RNA-seq analysis showed that TP upregulated autophagy and lysosome signal pathways, which was further confirmed through experiments. Immunofluorescence experiments indicated that TP activated transcription factor EB (TFEB), a key nuclear transcription factor modulating autophagy and lysosome biogenesis. In addition, TP inhibited the activity of mTOR, while it increased the expression of Lamp1. Furthermore, TP ameliorated the lysosomal damage and autophagy flux barrier caused by Baf A1 (lysosome inhibitor). Hence, our data suggested that TP repressed the proliferation of HCT116 cells by targeting lysosome to induce cytotoxic autophagy, which might be achieved through mTOR-TFEB signaling. In summary, TP may be used as a potential drug to overcome colon cancer.

摘要

靶向自噬和溶酶体可能成为癌症治疗的一种有前途的策略。茶多糖(TP)已显示出有希望的抗肿瘤作用。然而,其机制仍不清楚。本研究发现 TP 对结肠癌细胞系 HCT116 细胞的增殖有显著的抑制作用。RNA-seq 分析显示 TP 上调了自噬和溶酶体信号通路,通过实验进一步证实了这一点。免疫荧光实验表明,TP 激活了转录因子 EB(TFEB),TFEB 是调节自噬和溶酶体生物发生的关键核转录因子。此外,TP 抑制了 mTOR 的活性,同时增加了 Lamp1 的表达。此外,TP 改善了 Baf A1(溶酶体抑制剂)引起的溶酶体损伤和自噬流障碍。因此,我们的数据表明,TP 通过靶向溶酶体诱导细胞毒性自噬来抑制 HCT116 细胞的增殖,这可能是通过 mTOR-TFEB 信号通路实现的。综上所述,TP 可能被用作一种潜在的药物来克服结肠癌。

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