Ru(II)-Based Acetylacetonate Complexes Induce Apoptosis Selectively in Cancer Cells

被引:16
作者
Gupta, Sayak [1 ]
Vandevord, Jessica M. [2 ]
Loftus, Lauren M. [2 ]
Toupin, Nicholas [1 ]
Al-Afyouni, Malik H. [2 ]
Rohrabaugh, Thomas N., Jr. [2 ]
Turro, Claudia [2 ]
Kodanko, Jeremy J. [1 ]
机构
[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA
[2] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
RUTHENIUM(II) POLYPYRIDYL COMPLEXES; MITOCHONDRIAL DYSFUNCTION; ANTICANCER; CYTOTOXICITY; NECROPTOSIS; GENERATION; TOXICITY; DRUGS; DEATH; CURCUMIN;
D O I
10.1021/acs.inorgchem.1c02796
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis, chemical and biological characterization of seven Ru(II) polypyridyl complexes containing acetylacetonate (acac) ligands are reported. Electronic absorption spectra were determined and electrochemical potentials consistent with Ru(III/II) couples ranging from +0.60 to +0.73 V vs Ag/AgCl were measured. A series of complexes were screened against MDA-MB-231, DU-145, and MCF-10A cell lines to evaluate their cytotoxicities in cancer and normal cell lines. Although most complexes were either nontoxic or equipotent in cancer cells and normal cell lines, compound 1, [Ru(dpqy)(acac)(py)](PF6), where dqpy is 2,6-di(quinolin-2-yl)pyridine, showed up to 2.5:1.0 selectivity for cancer as compared to normal cells, along with nanomolar EC50 values in MDA-MB-231 cells. Lipophilicity, determined as the octanol/water partition coefficient, log P-o/w, ranged from -0.33 (0.06) to 1.15 (0.10) for the complexes. Although cytotoxicity was not correlated with electrochemical potentials, a moderate linear correlation between lipophilicity and toxicities was observed. Cell death mechanism studies indicated that several of the Ru-acac compounds, including 1, induce apoptosis in MDA-MB-231 cells.
引用
收藏
页码:18964 / 18974
页数:11
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