Syntheses, crystal structures of copper (II)-based complexes of sulfonamide derivatives and their anticancer effects through the synergistic effect of anti-angiogenesis, anti-inflammation, pro-apoptosis and cuproptosis

IF 5.9 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2024-12-15 Epub Date: 2024-10-10 DOI:10.1016/j.ejmech.2024.116954
Ai-Qiu Liao , Juan Wen , Jing-Chen Wei , Bing-Bing Xu , Nan Jin , Hong-Yu Lin , Xiu-Ying Qin
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Abstract

Three novel copper(II)-based complexes Cu-1, Cu-2, and Cu-3 containing sulfamethoxazole or sulfamethazine ligand were obtained, and their single structures were characterized. Both Cu-1 and Cu-3 show a broad spectrum of cytotoxicity than Cu-2, and Cu-1 is more cytotoxic than Cu-3. What's interesting is that Cu-1 can exhibit obvious inhibitory effect on the growth of human triple-negative breast cancer in vivo and vitro through anti-proliferative, anti-angiogenic, anti-inflammatory, pro-apoptotic and cuproptotic synergistic effects. Though Cu-3 shows no significant cytotoxicity against MDA-MB-231 cells, it can significantly inhibit the growth of SKOV3 cells in vitro by down-regulating the expression of some key proteins in the VEGF/VEGFR2 signaling pathway and the expression of some pro-inflammatory cytokines, and by disrupting the balance of intracellular reactive oxygen species levels.

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磺酰胺衍生物铜 (II) 基配合物的合成、晶体结构及其通过抗血管生成、抗炎、促凋亡和杯突变的协同效应发挥的抗癌作用
研究人员获得了含有磺胺甲噁唑或磺胺甲嗪配体的三种新型铜(II)基配合物 Cu-1、Cu-2 和 Cu-3,并对它们的单一结构进行了表征。与 Cu-2 相比,Cu-1 和 Cu-3 的细胞毒性范围更广,而 Cu-1 的细胞毒性比 Cu-3 更大。有趣的是,Cu-1 通过抗增殖、抗血管生成、抗炎、促凋亡和杯突协同作用,对人三阴性乳腺癌的体内和体外生长均有明显的抑制作用。虽然 Cu-3 对 MDA-MB-231 细胞没有明显的细胞毒性,但它能通过下调 VEGF/VEGFR2 信号通路中一些关键蛋白的表达和一些促炎细胞因子的表达,以及破坏细胞内活性氧水平的平衡,显著抑制 SKOV3 细胞在体外的生长。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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