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