Jiangxi Provincial Key Laboratory of Tumor Pathogens and Molecular Pathology and Department of Pathophysiology, Nanchang University Jiangxi Medical College, China.
Department of Gastroenterology, Research Institute of Digestive Diseases, The First Affiliated Hospital, Nanchang University, Nanchang, China.
Int J Biol Macromol. 2020 May 15;151:1277-1286. doi: 10.1016/j.ijbiomac.2019.10.174. Epub 2019 Nov 18.
The present study explores the mechanisms underlying the anti-cancer action of Inonotus obliquus polysaccharides (IOP). Thus, we characterized the IOP components extracted from Chaga sclerotium and, found that the extracts contained 70% polysaccharides with an average molecular weight of 4.5 × 10 Da consisting of 75% glucose. We then showed that IOP extract activated AMPK in lung cancer cells expressing LKB1, suppressed cell viability, colony-formation, and triggered cell apoptosis. In conjunction, IOP downregulated Bcl-2, upregulated Bax, and enhanced cleavage of Caspase-3 and PARP. All of these effects were prevented by treatment with Compound C, a chemical inhibitor of AMPK. IOP diminished mitochondrial membrane potential (MMP), concurrent with decreases in oxidative phosphorylation and glycolysis, which was dependent on LKB1/AMPK. Finally, IOP at a dosage of 50 mg/kg significantly inhibited allograft tumor growth of the LLC1 cells in association with increased apoptosis. Collectively, our results demonstrate that IOP acts on cancer cells through a mechanism by which AMPK triggers the apoptotic pathway via the opening of mitochondrial permeability transition pore, and reducing MMP, leading to an inhibition of ATP production. Therefore, our study provides a solid foundation for the use of IOP as a promising alternative or supplementary medicine for cancer therapy.
本研究探讨了桦褐孔菌多糖(IOP)抗癌作用的机制。因此,我们对桦褐孔菌菌核中提取的 IOP 成分进行了表征,发现提取物含有 70%的多糖,平均分子量为 4.5×10 Da,由 75%的葡萄糖组成。然后我们表明,IOP 提取物在表达 LKB1 的肺癌细胞中激活 AMPK,抑制细胞活力、集落形成,并触发细胞凋亡。同时,IOP 下调 Bcl-2,上调 Bax,并增强 Caspase-3 和 PARP 的裂解。所有这些作用都可以通过用 AMPK 的化学抑制剂 Compound C 处理来预防。IOP 降低了线粒体膜电位(MMP),同时伴随着氧化磷酸化和糖酵解的降低,这依赖于 LKB1/AMPK。最后,IOP 在 50mg/kg 的剂量下显著抑制 LLC1 细胞的同种异体移植肿瘤生长,同时增加凋亡。总的来说,我们的结果表明,IOP 通过一种机制作用于癌细胞,即 AMPK 通过打开线粒体通透性转换孔触发凋亡途径,并降低 MMP,从而抑制 ATP 产生。因此,我们的研究为将 IOP 用作癌症治疗的一种有前途的替代或补充药物提供了坚实的基础。