Department of Bioengineering, Faculty of Engineering, İzmir Institute of Technology, 35430, Urla, İzmir, Turkey.
Department of Bioengineering, Faculty of Engineering, Gebze Technical University, 41400, Gebze, Kocaeli, Turkey.
Sci Rep. 2022 Aug 16;12(1):13834. doi: 10.1038/s41598-022-17977-4.
The discovery of novel chemotherapeutics that act through different mechanisms is critical for dealing with tumor heterogeneity and therapeutic resistance. We previously reported a saponin analog (AG-08) that induces non-canonical necrotic cell death and is auspicious for cancer therapy. Here, we describe that the key element in triggering this unique cell death mechanism of AG-08 is its ability to form supramolecular particles. These self-assembled particles are internalized via a different endocytosis pathway than those previously described. Microarray analysis suggested that AG-08 supramolecular structures affect several cell signaling pathways, including unfolded protein response, immune response, and oxidative stress. Finally, through investigation of its 18 analogs, we further determined the structural features required for the formation of particulate structures and the stimulation of the unprecedented cell death mechanism of AG-08. The unique results of AG-08 indicated that supramolecular assemblies of small molecules are promising for the field of anticancer drug development, although they have widely been accepted as nuisance in drug discovery studies.
发现作用机制不同的新型化疗药物对于应对肿瘤异质性和治疗抵抗至关重要。我们之前报道了一种皂苷类似物(AG-08),它能诱导非典型的坏死性细胞死亡,对癌症治疗有好处。在这里,我们描述了触发 AG-08 这种独特细胞死亡机制的关键因素是它形成超分子颗粒的能力。这些自组装颗粒通过不同于先前描述的内吞作用途径被内化。微阵列分析表明,AG-08 超分子结构影响几种细胞信号通路,包括未折叠蛋白反应、免疫反应和氧化应激。最后,通过对其 18 种类似物的研究,我们进一步确定了形成颗粒状结构和刺激 AG-08 前所未有的细胞死亡机制所需的结构特征。AG-08 的独特结果表明,尽管小分子的超分子组装在药物发现研究中被广泛认为是一种干扰,但它们在抗癌药物开发领域具有广阔的前景。