School of Chemistry, University of Leicester, Leicester, LE1 7RH, UK.
Dalton Trans. 2024 Apr 2;53(14):6410-6415. doi: 10.1039/d4dt00384e.
An asymmetric bi-nuclear copper(II) complex with both cytotoxic and immunogenic activity towards breast cancer stem cells (CSCs) is reported. The bi-nuclear copper(II) complex comprises of two copper(II) centres bound to flufenamic acid and 3,4,7,8-tetramethyl-1,10-phenanthroline. The bi-nuclear copper(II) complex exhibits sub-micromolar potency towards breast CSCs grown in monolayers and three-dimensional cultures. Remarkably, the bi-nuclear copper(II) complex is up to 25-fold more potent toward breast CSC mammospheres than salinomycin (a gold standard anti-breast CSC agent) and cisplatin (a clinically administered metallodrug). Mechanistic studies showed that the bi-nuclear copper(II) complex readily enters breast CSCs, elevates intracellular reactive oxygen species levels, induces apoptosis, and promotes damage-associated molecular pattern release. The latter triggers phagocytosis of breast CSCs by macrophages. As far as we are aware, this is the first report of a bi-nuclear copper(II) complex to induce engulfment of breast CSCs by immune cells.
报道了一种具有细胞毒性和免疫原性的不对称双核铜(II)配合物,针对乳腺癌干细胞(CSC)。双核铜(II)配合物由两个铜(II)中心与氟芬那酸和 3,4,7,8-四甲基-1,10-菲咯啉结合而成。双核铜(II)配合物对单层和三维培养的乳腺癌 CSCs 的生长具有亚微米级的效力。值得注意的是,双核铜(II)配合物对乳腺癌 CSC 类球体的效力比黏菌素(一种金标准的抗乳腺癌 CSC 试剂)和顺铂(一种临床使用的金属药物)高 25 倍。机制研究表明,双核铜(II)配合物容易进入乳腺癌 CSCs,提高细胞内活性氧水平,诱导细胞凋亡,并促进损伤相关分子模式的释放。后者触发巨噬细胞吞噬乳腺癌 CSCs。据我们所知,这是首例报道双核铜(II)配合物诱导免疫细胞吞噬乳腺癌 CSCs 的报告。