Recent Progress in Polynuclear Ruthenium Complex-Based DNA Binders/Structural Probes and Anticancer Agents

被引:22
作者
Zhang, Si-Qi [1 ]
Gao, Li-Hua [2 ]
Zhao, Hua [2 ]
Wang, Ke-Zhi [1 ]
机构
[1] Beijing Normal Univ, Key Lab Radiopharmaceut, Minist Educ, Coll Chem, Beijing 100875, Peoples R China
[2] Beijing Technol & Business Univ, Sch Sci, Key Lab Cosmet, China Natl Light Ind, Beijing 100048, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Ruthenium; DNA; DNA structural probe; cytotoxicity; binding mode; Cisplatin-based drugs; anticancer drugs; CELLULAR UPTAKE; POLYPYRIDYL COMPLEXES; IN-VITRO; RU(II)-PT(II) SUPRAMOLECULE; THREADING INTERCALATION; BINDING PROPERTIES; RED-LIGHT; PHASE-I; METAL; PHOTOCLEAVAGE;
D O I
10.2174/0929867326666181203143422
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ruthenium complexes have stood out by several mononuclear complexes which have entered into clinical trials, such as imidazolium [trans-RuCl4(1H-imidazole)(DMSO-S)] (NAMI-A) and ([Ru(II)(4,4'-dimethyl-2,2'-bipyridine)2-(2(2'-,2 '':5 '',2'''-terthiophene)-imidazo[4,5-f] [1,10]phenanthroline)](2+)) (TLD-1433), opening a new avenue for developing promising ruthenium-based anticancer drugs alternative to Cisplatin. Polynuclear ruthenium complexes were reported to exhibit synergistic and/or complementary effects: the enhanced DNA structural recognition and DNA binding as well as in vitro anticancer activities. This review overviews some representative polynuclear ruthenium complexes acting as DNA structural probes, DNA binders and in vitro anticancer agents, which were developed during last decades. These complexes are reviewed according to two main categories of homo-polynuclear and hetero-polynuclear complexes, each of which is further clarified into the metal centers linked by rigid and flexible bridging ligands. The perspective, challenges and future efforts for investigations into these exciting complexes are pointed out or suggested.
引用
收藏
页码:3735 / 3752
页数:18
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