Huang Minjian, Liu Bo, Liu Ran, Li Jian, Chen Jilei, Jiang Fenglei, Ding Hong, Deng Zixin, Liu Tiangang
Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Ministry of Education), School of Pharmaceutical Sciences, Wuhan University, Wuhan, 430071, China.
J1 Biotech Co., Ltd., Wuhan 430075, China.
ACS Pharmacol Transl Sci. 2018 Oct 12;1(2):84-95. doi: 10.1021/acsptsci.8b00007. eCollection 2018 Nov 9.
The potential of the polyether salinomycin as an inhibitory agent against cancer stem cells has attracted interest in this family of compounds. In this study, we found that the aglycone polyether nanchangmycin and its homologues show promising activities against breast cancer stem cells as well as 38 other different types of cancer cells by assays. We found that aglycone polyethers caused elevations in calcium levels, an accumulation of reactive oxygen species and mitochondrial inner membrane permeability to H and K, resulting in the release of cytochrome and apoptosis-inducing factor and the triggering of caspase-dependent apoptosis. Our analyses also indicate that aglycone polyethers are potent Wnt/β-catenin signaling inhibitors, blocking the Wnt pathway and resulting in reduced cell survival. Notably, the key autophagy-related proteins LC3A/B were also activated by aglycone polyether treatment. Furthermore, nanchangmycin showed inhibitory effects toward somatic tumors developed from MCF-7 paclitaxel-resistant breast cancer cells injected into BALB/c mice. Our study not only provides promising candidates for therapy against cancer stem cells but also provides the groundwork for identifying stronger therapeutic agents among the natural polyether compounds.
聚醚盐霉素作为一种抗癌干细胞抑制剂的潜力,引起了人们对这类化合物的关注。在本研究中,我们发现糖苷配基聚醚南昌霉素及其同系物通过实验显示出对乳腺癌干细胞以及其他38种不同类型癌细胞具有良好的活性。我们发现糖苷配基聚醚会导致钙水平升高、活性氧积累以及线粒体内膜对H和K的通透性增加,从而导致细胞色素和凋亡诱导因子的释放,并引发半胱天冬酶依赖性凋亡。我们的分析还表明,糖苷配基聚醚是有效的Wnt/β-连环蛋白信号抑制剂,可阻断Wnt通路并导致细胞存活率降低。值得注意的是,关键的自噬相关蛋白LC3A/B也被糖苷配基聚醚处理激活。此外,南昌霉素对注射到BALB/c小鼠体内的MCF-7耐紫杉醇乳腺癌细胞形成的实体瘤显示出抑制作用。我们的研究不仅为抗癌干细胞治疗提供了有前景的候选药物,也为在天然聚醚化合物中鉴定更强效的治疗药物奠定了基础。