Alajroush Duaa R, Anderson Brittney F, Bruce Janae A, Lartey Christian I, Mathurin Dazonte A, Washington Sean T, Washington Tanaya S, Diawara Sidy, Waheed Sakariyau A, Thomas Kaylin L, Beebe Stephen J, Holder Alvin A
Department of Chemistry and Biochemistry, Old Dominion University 4501 Elkhorn Avenue, Norfolk, VA 23529, USA.
Department of Biological Sciences, University of the Virgin Islands, 2 John Brewers Bay, St. Thomas, VI 00802, USA.
Results Chem. 2024 Dec;12. doi: 10.1016/j.rechem.2024.101882. Epub 2024 Oct 30.
In this study, the copper(II) complex [Cu(chromoneTSC)Cl]•0.5HO•0.0625CHOH (where chromoneTSC = -Ethyl-2-((4-oxo-4H-chromen-3-yl)methylene)-hydrazinecarbothioamide) was synthesized and characterized; then used to carry out studies in combination with berberine chloride (BBC). The ligand and complex were characterized by elemental analysis, FTIR and NMR (H and C) spectroscopy, and conductivity measurements. The cytotoxic effect was analyzed by using the CCK-8 viability assay in cancer MDA-MB-231 VIM RFP and non-cancer MCF-10A cell lines. The IC values for the complex and BBC were 21.2 ±1.6 and 48.3 ± 2.4 μM, respectively at 24 h incubation, while the IC value of the combination treatment was 9.3 ± 1.5 in cancer cells. The co-treatment group significantly increased the number of cells in G2 phase, indicating the growth arrest of cancer cells. Moreover, the combination group showed induction of both intrinsic and extrinsic apoptotic pathways. There was also a study on the effect of the combination treatment on receptor-interacting serine/threonine-protein kinase 3 (RIPK3) and mixed lineage kinase domain-like pseudokinase (MLKL) as biomarkers of necroptosis. The results showed activation of necroptosis after treatment with the combination of the copper complex and BBC the activation of RIPK3-MLKL pathway.
在本研究中,合成并表征了铜(II)配合物[Cu(色酮TSC)Cl]•0.5HO•0.0625CHOH(其中色酮TSC = -乙基-2-((4-氧代-4H-色烯-3-基)亚甲基)-肼基甲硫酰胺);然后将其与盐酸小檗碱(BBC)联合进行研究。通过元素分析、傅里叶变换红外光谱(FTIR)和核磁共振(H和C)光谱以及电导率测量对配体和配合物进行了表征。使用CCK-8活力测定法分析了在癌症MDA-MB-231 VIM RFP和非癌症MCF-10A细胞系中的细胞毒性作用。在孵育24小时时,配合物和BBC的半数抑制浓度(IC)值分别为21.2±1.6和48.3±2.4μM,而联合治疗在癌细胞中的IC值为9.3±1.5。联合治疗组显著增加了处于G2期的细胞数量,表明癌细胞生长停滞。此外,联合治疗组显示出诱导了内源性和外源性凋亡途径。还研究了联合治疗对作为坏死性凋亡生物标志物的受体相互作用丝氨酸/苏氨酸蛋白激酶3(RIPK3)和混合谱系激酶结构域样假激酶(MLKL)的影响。结果表明,铜配合物与BBC联合治疗后激活了坏死性凋亡——RIPK3-MLKL途径的激活。