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钌(II)-三吡唑基甲烷配合物通过破坏线粒体钙稳态抑制癌细胞生长。

Ruthenium(II)-Tris-pyrazolylmethane Complexes Inhibit Cancer Cell Growth by Disrupting Mitochondrial Calcium Homeostasis.

机构信息

Czech Academy of Sciences, Institute of Biophysics, Kralovopolska 135, CZ-61265 Brno, Czech Republic.

Faculty of Science, Department of Biochemistry, Masaryk University, Kamenice 5, CZ-62500 Brno, Czech Republic.

出版信息

J Med Chem. 2022 Aug 11;65(15):10567-10587. doi: 10.1021/acs.jmedchem.2c00722. Epub 2022 Aug 1.

Abstract

While ruthenium arene complexes have been widely investigated for their medicinal potential, studies on homologous compounds containing a tridentate tris(1-pyrazolyl)methane ligand are almost absent in the literature. Ruthenium(II) complex was obtained by a modified reported procedure; then, the reactions with a series of organic molecules (L) in boiling alcohol afforded novel complexes - in 77-99% yields. Products were fully structurally characterized. They are appreciably soluble in water, where they undergo partial chloride/water exchange. The antiproliferative activity was determined using a panel of human cancer cell lines and a noncancerous one, evidencing promising potency of , , and and significant selectivity toward cancer cells. The tested compounds effectively accumulate in cancer cells, and mitochondria represent a significant target of biological action. Most notably, data provide convincing evidence that the mechanism of biological action is mediated by the inhibiting of mitochondrial calcium intake.

摘要

虽然钌芳配合物因其药用潜力而被广泛研究,但含三齿三(1-吡唑基)甲烷配体的同系物的研究在文献中几乎不存在。通过改进的报道程序获得了钌(II)配合物 ;然后,在沸腾的醇中与一系列有机分子 (L) 反应,以 77-99%的收率得到了新型配合物-。产物 进行了充分的结构表征。它们在水中具有相当好的溶解性,在水中会发生部分氯化物/水交换。使用一组人类癌细胞系和一个非癌细胞系测定了增殖活性,证明 、 、 和 的潜力很大,对癌细胞具有显著的选择性。测试化合物有效地在癌细胞中积累,线粒体是生物作用的重要靶点。值得注意的是,数据提供了令人信服的证据,表明生物作用的机制是通过抑制线粒体钙摄取来介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23bc/9376960/247f3329c0c7/jm2c00722_0011.jpg

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