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Salinomycin co-treatment enhances tamoxifen cytotoxicity in luminal A breast tumor cells by facilitating lysosomal degradation of receptor tyrosine kinases.沙利霉素联合治疗通过促进受体酪氨酸激酶的溶酶体降解增强他莫昔芬对腔面A型乳腺肿瘤细胞的细胞毒性。
Oncotarget. 2016 Aug 2;7(31):50461-50476. doi: 10.18632/oncotarget.10459.
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A comprehensive review of glycosylated bacterial natural products.糖基化细菌天然产物的全面综述。
Chem Soc Rev. 2015 Nov 7;44(21):7591-697. doi: 10.1039/c4cs00426d.
3
Anticancer Activity of Polyether Ionophore-Salinomycin.聚醚离子载体-沙利霉素的抗癌活性
Anticancer Agents Med Chem. 2015;15(5):575-91. doi: 10.2174/1871520615666150101130209.
4
Salinomycin exerts anticancer effects on human breast carcinoma MCF-7 cancer stem cells via modulation of Hedgehog signaling.沙利霉素通过调节 Hedgehog 信号通路对人乳腺癌 MCF-7 肿瘤干细胞发挥抗癌作用。
Chem Biol Interact. 2015 Feb 25;228:100-7. doi: 10.1016/j.cbi.2014.12.002. Epub 2014 Dec 8.
5
Co-delivery of all-trans-retinoic acid and doxorubicin for cancer therapy with synergistic inhibition of cancer stem cells.载阿霉素和全反式维甲酸的药物共传递用于癌症治疗并协同抑制肿瘤干细胞。
Biomaterials. 2015 Jan;37:405-14. doi: 10.1016/j.biomaterials.2014.10.018. Epub 2014 Oct 23.
6
Sensitization of cancer cells through reduction of total Akt and downregulation of salinomycin-induced pAkt, pGSk3β, pTSC2, and p4EBP1 by cotreatment with MK-2206.通过与MK-2206联合处理降低总Akt水平以及下调沙林霉素诱导的pAkt、pGSk3β、pTSC2和p4EBP1来使癌细胞致敏。
Biomed Res Int. 2014;2014:295760. doi: 10.1155/2014/295760. Epub 2014 Jul 8.
7
Tackling the cancer stem cells - what challenges do they pose?攻克癌症干细胞——它们带来了哪些挑战?
Nat Rev Drug Discov. 2014 Jul;13(7):497-512. doi: 10.1038/nrd4253.
8
Salinomycin suppresses LRP6 expression and inhibits both Wnt/β-catenin and mTORC1 signaling in breast and prostate cancer cells.沙利霉素可抑制乳腺癌和前列腺癌细胞中低密度脂蛋白受体相关蛋白6(LRP6)的表达,并抑制Wnt/β-连环蛋白和mTORC1信号通路。
J Cell Biochem. 2014 Oct;115(10):1799-807. doi: 10.1002/jcb.24850.
9
Salinomycin activates AMP-activated protein kinase-dependent autophagy in cultured osteoblastoma cells: a negative regulator against cell apoptosis.黏菌素激活培养成骨肉瘤细胞中 AMP 激活的蛋白激酶依赖性自噬:细胞凋亡的负调节剂。
PLoS One. 2013 Dec 17;8(12):e84175. doi: 10.1371/journal.pone.0084175. eCollection 2013.
10
Salinomycin induces cell death with autophagy through activation of endoplasmic reticulum stress in human cancer cells.沙利霉素通过激活内质网应激诱导人癌细胞自噬性死亡。
Autophagy. 2013 Jul;9(7):1057-68. doi: 10.4161/auto.24632. Epub 2013 Apr 18.

苷元型聚醚南昌霉素及其同系物对癌症干细胞具有凋亡和抗增殖活性。

Aglycone Polyether Nanchangmycin and Its Homologues Exhibit Apoptotic and Antiproliferative Activities against Cancer Stem Cells.

作者信息

Huang Minjian, Liu Bo, Liu Ran, Li Jian, Chen Jilei, Jiang Fenglei, Ding Hong, Deng Zixin, Liu Tiangang

机构信息

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.

出版信息

ACS Pharmacol Transl Sci. 2018 Oct 12;1(2):84-95. doi: 10.1021/acsptsci.8b00007. eCollection 2018 Nov 9.

DOI:10.1021/acsptsci.8b00007
PMID:32219205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7088892/
Abstract

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.

摘要

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。