含有3,3 ' -二羧基-2,2 ' -联吡啶配体的钌配合物(II)的抗癌和抗增殖活性

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Mohamed Saadh
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引用次数: 0

摘要

尽管癌症治疗已经取得了重大进展,但仍有改进的余地。实验药物钌复合物II显示出治疗癌症的希望。本文合成了二氯-3,3′-二羧基-2,2′-联吡啶基双(二甲基亚砜)钌(II) [RuCl 2(3,3′-dcbpy)(DMSO) 2],并对其对MDA-MB-231和MRC-5细胞系的抗癌活性、作用机制和选择性进行了研究。研究发现,[RuCl 2(3,3′-dcbpy)(DMSO) 2]对MDA-MB-231细胞毒性高,对MRC-5细胞毒性最低,ic50值分别为5.95和579.6 μg/ml。钌络合物II在破坏癌细胞方面非常有效,同时对健康细胞的危害最小。RuCl 2 (3,3 ' -dcbpy)(DMSO) 2]引起细胞凋亡,通过激活caspase-3证实了这一点。钌络合物作为强效抗癌剂具有很大的前景。它们独特的作用机制、选择性靶向癌细胞的能力以及化学结构的多功能性使它们成为靶向治疗发展的有吸引力的候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticancer and antiproliferative activity of ruthenium complex (II) bearing 3,3’-dicarboxy-2,2’-bipyridine ligand
Even though significant progress has been made in cancer treatment, there is always room for improvement. The experimental drug Ruthenium Complex II shows promise as a cancer treatment. In this article, the dichloro-3,3’-dicarboxy-2,2’-bipyridyl bis(dimethylsulphoxide)ruthenium(II) [RuCl 2 (3,3’-dcbpy)(DMSO) 2 ], have been synthesized, characterized, and studied for its anticancer activity against MDA-MB-231 and MRC-5 cell lines, as well as its mechanisms of action and selectivity. According to research, [RuCl 2 (3,3’-dcbpy)(DMSO) 2 ], is highly cytotoxic to the MDA-MB-231 and minimum cytotoxic to MRC-5 cell lines, with IC 50 values of 5.95 and 579.6 μg/ml, respectively. Ruthenium Complex II is exceptionally effective at destroying cancer cells while causing minimal harm to healthy cells. RuCl 2 (3,3’-dcbpy)(DMSO) 2 ] caused apoptosis, which was confirmed by the activation of caspase-3. Ruthenium complexes hold great promise as powerful anticancer agents. Their unique mechanisms of action, ability to selectively target cancer cells, and versatility in chemical structure make them attractive candidates for the development of targeted therapies.
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来源期刊
Pharmacia
Pharmacia PHARMACOLOGY & PHARMACY-
CiteScore
2.30
自引率
27.30%
发文量
114
审稿时长
12 weeks
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