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2,6-双(2-苯并咪唑基)吡啶作为潜在抗癌剂的新型锰(II)、铁(II)、钴(II)、镍(II)和铜(II)邻苯甲酰甲酸盐配合物。

New manganese(II), iron(II), cobalt(II), nickel(II) and copper(II) saccharinate complexes of 2,6-bis(2-benzimidazolyl)pyridine as potential anticancer agents.

机构信息

Department of Chemistry, Faculty of Arts and Sciences, Bursa Uludag University, 16059, Bursa, Turkey.

Department of Chemistry, Faculty of Arts and Sciences, Bursa Uludag University, 16059, Bursa, Turkey.

出版信息

Eur J Med Chem. 2020 Sep 15;202:112535. doi: 10.1016/j.ejmech.2020.112535. Epub 2020 Jul 3.

DOI:10.1016/j.ejmech.2020.112535
PMID:32653697
Abstract

New mononuclear complexes [Mn(NO)(sac)(HO)(bzimpy)]·2DMF (Mn), [Fe(sac)(HO)(bzimpy)]·2HO (Fe), Co(bzimpy)·2HO (Co), Ni(bzimpy)·HO·i-PrOH (Ni) and [Cu(sac)(bzimpy)]·3DMF (Cu) (sac = saccharinate and bzimpy = 2,6-bis(2-benzimidazolyl)pyridine) were synthesized and structurally characterized by elemental analysis, UV-Vis, IR, ESI-MS and X-ray diffraction. The anticancer activity of the metal complexes against A549 (lung), MCF-7 (breast), HT29 (colon) cancer cells and MCF10A (normal human breast epithelial) cells was tested and compared with those of cisplatin and bzimpy. The complexes displayed potent cytotoxic activity especially in MCF-7 and A549 cell lines, but they were practically inactive against the normal cells. Mechanistic studies with Mn and Cu complexes on A549 cells indicated that the complexes induced G0/G1 arrest. Both complexes increased intracellular ROS (reactive oxygen species) levels and successfully caused both mitochondrial dysfunction and double-strand DNA breaks. The up-regulated Bax and down-regulated Bcl-2 expression levels, caspase-3/7 activation and reduced Fas expression indicated that Mn and Cu induced ROS-dependent mitochondria-mediated intrinsic apoptosis in A549 cells.

摘要

新单核配合物[Mn(NO)(sac)(HO)(bzimpy)]·2DMF(Mn),[Fe(sac)(HO)(bzimpy)]·2HO(Fe),Co(bzimpy)·2HO(Co),Ni(bzimpy)·HO·i-PrOH(Ni)和[Cu(sac)(bzimpy)]·3DMF(Cu)(sac= saccharinate,bzimpy=2,6-双(2-苯并咪唑基)吡啶)被合成并通过元素分析、UV-Vis、IR、ESI-MS 和 X 射线衍射进行了结构表征。测试了金属配合物对 A549(肺)、MCF-7(乳腺)、HT29(结肠)癌细胞和 MCF10A(正常人类乳腺上皮)细胞的抗癌活性,并与顺铂和 bzimpy 进行了比较。这些配合物表现出很强的细胞毒性活性,特别是在 MCF-7 和 A549 细胞系中,但对正常细胞实际上没有活性。用 Mn 和 Cu 配合物对 A549 细胞进行的机制研究表明,这些配合物诱导了 G0/G1 期停滞。两种配合物均增加了细胞内 ROS(活性氧)水平,并成功导致线粒体功能障碍和双链 DNA 断裂。上调的 Bax 和下调的 Bcl-2 表达水平、caspase-3/7 激活和 Fas 表达减少表明,Mn 和 Cu 诱导了 A549 细胞中 ROS 依赖性线粒体介导的内在细胞凋亡。

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