Exploring six-coordinate germanium(IV)-diketonate complexes as anticancer agents

被引:12
|
作者
Mertens, Randall T. [1 ]
Parkin, Sean [1 ]
Awuah, Samuel G. [1 ]
机构
[1] Univ Kentucky, Coll Arts & Sci, Dept Chem, 505 Rose St, Lexington, KY 40506 USA
关键词
Germanium; Anticancer; Metalloid; Cytotoxicity; Drug discovery; Resistance; ACUTE PROMYELOCYTIC LEUKEMIA; MOLECULAR-STRUCTURE; N-METHYLFORMAMIDE; CRYSTAL-STRUCTURE; OXIDATIVE STRESS; ARSENIC TRIOXIDE; PHASE-II; GERMANIUM; CISPLATIN; SPIROGERMANIUM;
D O I
10.1016/j.ica.2019.119375
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Cancer remains one of the leading causes of death worldwide and despite several attempts using chemotherapy to combat the deadly disease, toxic side effects and drug resistance temper efficacy [1]. Thus, drugs with potentially new mechanisms and lower toxicity to normal cells are needed. Metalloids such as arsenic compounds have been clinically beneficial in fighting cancer, but germanium is yet to gain such prominence [2,3]. We report the synthesis of four octahedral germanium(IV) complexes bearing acetylacetonato ligand, [Ge-IV(acac)(3))](+), with different anions (3 - 6) using a streamlined synthetic approach. The compounds were structurally and electrochemically characterized using NMR, MS, X-ray crystallography, and cyclic voltammetry. The cyclic voltammogram of 3-5 revealed distinct irreversible peaks in the range of - 0.9 to - 1.9 V, corresponding to Ge(IV)/Ge(II) or Ge(II)/Ge(0) couple in DMSO. We explored the anticancer activity of the complexes against a panel of cancer cell lines with IC50 values in the sub-micromolar range (9-15 mu M). The compounds display similar to 3-fold selectivity in cancer cells over normal epithelial cells. In addition to the promising anticancer activity, the compounds display high complex stability in biological media, induces G1 arrest, reactive oxygen stress (ROS) accumulation, and mitochondria membrane depolarization in cancer cells. Furthermore, the compounds induce significant apoptosis.
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页数:11
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