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辅助配体在确定噻唑烷酮 Pd(II)配合物的遗传毒性和细胞死亡方式中的作用。

Role of the auxiliary ligand in determining the genotoxicity and mode of cell death of thiosemicarbazone Pd(II) complexes.

机构信息

Department of Chemistry, United Arab Emirates University, Al-Ain, United Arab Emirates.

Department of Chemistry, Faculty of Science, Cairo University, Gamma Street, Giza, Cairo 12613, Egypt.

出版信息

Dalton Trans. 2024 Mar 12;53(11):5073-5083. doi: 10.1039/d4dt00032c.

Abstract

A series of Pd(II) complexes of the general formula [PdX(NNS)] (X = Cl, Br, I, NCS and phenyl-tetrazole-thiolato; NNS = 2-quinolinecarboxyaldehyde--phenylthiosemicarbazone) was tested against four malignant cell lines for their antiproliferative properties and the outcomes were compared to those seen in normal mouse splenocytes. Various auxiliary ligands were substituted in order to investigate the impact of the character of the ligand on the cytotoxicity of this class of Pd(II) complexes. The iodo complex was the most cytotoxic compound towards the Caco-2 cell line in this study. The improved apoptosis and necrosis cell modes were in accordance with the fragmentation results of DNA, which revealed increased fragmentation terminals, especially in isothiocyanate and tetrazole-thiolato complexes. After 24 hours, at half the IC of each complex, the complex-treated cells exhibited considerable genotoxicity when compared to the corresponding non-treated control especially in the case of isothiocyanate and tetrazole-thiolato complexes.

摘要

一系列通式为[PdX(NNS)]的 Pd(II) 配合物(X = Cl、Br、I、NCS 和苯并四唑硫醇;NNS = 2-喹啉羧酸醛-苯并噻唑缩氨硫脲)被测试了其对四种恶性细胞系的抗增殖特性,结果与正常小鼠脾细胞的结果进行了比较。为了研究配体的性质对这类 Pd(II) 配合物的细胞毒性的影响,我们取代了各种辅助配体。在这项研究中,碘配合物对 Caco-2 细胞系的细胞毒性最强。改进的凋亡和坏死细胞模式与 DNA 的片段化结果一致,这表明特别是在异硫氰酸酯和四唑硫醇配合物中,片段化末端增加。在每个配合物的 IC 的一半后,与相应的未经处理的对照相比,经处理的细胞在 24 小时后表现出相当大的遗传毒性,特别是在异硫氰酸酯和四唑硫醇配合物的情况下。

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