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作为一种前所未有的作用模式被观察到的副凋亡性细胞死亡:含膦配体的新型联吡啶-银(I)化合物

Paraptotic Cell Death as an Unprecedented Mode of Action Observed for New Bipyridine-Silver(I) Compounds Bearing Phosphane Coligands.

作者信息

Teixeira Ricardo G, Stefanelli Alessia, Pilon Adhan, Warmers Rebecca, Fontrodona Xavier, Romero Isabel, Costa Paulo J, Villa de Brito Maria J, Hudec Xenia, Pirker Christine, Türck Sebastian, Antunes Alexandra M M, Kowol Christian R, Ott Ingo, Brozovic Anamaria, Sombke Andy, Eckhard Margret, Tomaz Ana Isabel, Heffeter Petra, Valente Andreia

机构信息

Centro de Química Estrutural, Institute of Molecular Sciences, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, Campo Grande, Lisboa 1749-016, Portugal.

Center for Cancer Research and Comprehensive Cancer Center, Medical University of Vienna, Vienna 1090, Austria.

出版信息

J Med Chem. 2024 Apr 25;67(8):6081-6098. doi: 10.1021/acs.jmedchem.3c01036. Epub 2024 Feb 24.

Abstract

In this work, we investigated the anticancer activity of several novel silver(I) 2,2'-bipyridine complexes containing either triphenylphosphane (PPh) or 1,2-bis(diphenylphosphino)ethane (dppe) ligands. All compounds were characterized by diverse analytical methods including ESI-MS spectrometry; NMR, UV-vis, and FTIR spectroscopies; and elemental analysis. Moreover, several compounds were also studied by X-ray single-crystal diffraction. Subsequently, the compounds were investigated for their anticancer activity against drug-resistant and -sensitive cancer cells. Noteworthily, neither carboplatin and oxaliplatin resistance nor p53 deletion impacted on their anticancer efficacy. MESOV cells displayed exceptional hypersensitivity to the dppe-containing drugs. This effect was not based on thioredoxin reductase inhibition, enhanced drug uptake, or apoptosis induction. In contrast, dppe silver drugs induced paraptosis, a novel recently described form of programmed cell death. Together with the good tumor specificity of this compound's class, this work suggests that dppe-containing silver complexes could be interesting drug candidates for the treatment of resistant ovarian cancer.

摘要

在本研究中,我们研究了几种新型含三苯基膦(PPh)或1,2 - 双(二苯基膦基)乙烷(dppe)配体的银(I)2,2'-联吡啶配合物的抗癌活性。所有化合物均通过多种分析方法进行表征,包括电喷雾质谱(ESI-MS);核磁共振(NMR)、紫外可见(UV-vis)和傅里叶变换红外(FTIR)光谱;以及元素分析。此外,还通过X射线单晶衍射对几种化合物进行了研究。随后,研究了这些化合物对耐药和敏感癌细胞的抗癌活性。值得注意的是,卡铂和奥沙利铂耐药以及p53缺失均未影响其抗癌疗效。MESOV细胞对含dppe的药物表现出异常的超敏感性。这种效应并非基于硫氧还蛋白还原酶抑制、增强的药物摄取或凋亡诱导。相反,含dppe的银药物诱导了类凋亡,这是一种最近描述的新型程序性细胞死亡形式。鉴于该类化合物具有良好的肿瘤特异性,本研究表明含dppe的银配合物可能是治疗耐药卵巢癌的有前景的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d560/11056982/058fb14ee898/jm3c01036_0001.jpg

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