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一种新型皂草苷元衍生物通过增强蛋白水解作用触发非经典坏死性细胞死亡的鉴定

Identification of a Noncanonical Necrotic Cell Death Triggered via Enhanced Proteolysis by a Novel Sapogenol Derivative.

作者信息

Üner Göklem, Tag Özgür, Erzurumlu Yalçın, Kirmizibayrak Petek Ballar, Bedir Erdal

机构信息

Department of Bioengineering, Izmir Institute of Technology, 35430 Urla-İzmir, Turkey.

Bionorm Natural Products Production & Marketing Corporation, ITOB, 35477 Menderes-İzmir, Turkey.

出版信息

Chem Res Toxicol. 2020 Nov 16;33(11):2880-2891. doi: 10.1021/acs.chemrestox.0c00339. Epub 2020 Nov 2.

Abstract

Small molecules which activate distinct cell death pathways have promising high potential for anticancer drug research. Especially, regulated necrosis draws attention as an alternative cell death mechanism to overcome the drug resistance. Here, we report that a new semisynthetic saponin analogue (AG-08) triggers necrotic cell death with unprecedented pathways. AG-08-mediated necrosis depends on enhanced global proteolysis involving calpains, cathepsins, and caspases. Moreover, AG-08 generates several alterations in lysosomal function and physiology including membrane permeabilization, redistribution toward the perinuclear area, and lastly excessive tubulation. As a consequence of lysosomal impairment, the autophagic process was abolished via AG-08 treatment. Collectively, in addition to its ability to induce necrotic cell death, which makes AG-08 a promising candidate to cope with drug resistance, its unique activity mechanisms including autophagy/lysosome impairment and enhancement of proteolysis leading a strong death capacity emphasizes its potential for anticancer drug research.

摘要

激活不同细胞死亡途径的小分子在抗癌药物研究中具有很高的潜力。特别是,调节性坏死作为一种克服耐药性的替代性细胞死亡机制受到关注。在此,我们报告一种新的半合成皂苷类似物(AG-08)通过前所未有的途径引发坏死性细胞死亡。AG-08介导的坏死依赖于涉及钙蛋白酶、组织蛋白酶和半胱天冬酶的整体蛋白水解增强。此外,AG-08在溶酶体功能和生理学方面产生了多种改变,包括膜通透性增加、向核周区域重新分布,以及最终过度形成管状结构。由于溶酶体受损,通过AG-08处理消除了自噬过程。总体而言,除了其诱导坏死性细胞死亡的能力(这使AG-08成为应对耐药性的有希望的候选物)外,其独特的活性机制,包括自噬/溶酶体损伤和蛋白水解增强导致强大的死亡能力,强调了其在抗癌药物研究中的潜力。

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