Li Yang, Dong Jianfang, Zhao Peiran, Hu Ping, Yang Dawei, Gao Lei, Li Lianzhi
Zhong Yuan Academy of Biological Medicine, Liaocheng People's Hospital, Liaocheng 252000, China.
Department of Material Science, Shandong Polytechnic Technician College, Liaocheng 252000, China.
Bioinorg Chem Appl. 2020 Sep 29;2020:8834859. doi: 10.1155/2020/8834859. eCollection 2020.
Three hexacoordinated octahedral nickel (II) complexes, [Ni (Trp-sal) (phen) (CHOH)] (1), [Ni (Trp--van) (phen) (CHOH)]•2CHOH (2), and [Ni (Trp-naph) (phen) (CHOH)] (3) (where Trp-sal = Schiff base derived from tryptophan and salicylaldehyde, Trp--van = Schiff base derived from tryptophan and -vanillin, Trp-naph = Schiff base derived from tryptophan and 2-hydroxy-1-naphthaldehyde, phen = 1, 10-phenanthroline), have been synthesized and characterized as potential anticancer agents. Details of structural study of these complexes using single-crystal X-ray crystallography showed that distorted octahedral environment around nickel (II) ion has been satisfied by three nitrogen atoms and three oxygen atoms. All these complexes displayed moderate cytotoxicity toward esophageal cancer cell line Eca-109 with the IC values of 23.95 ± 2.54 M for 1, 18.14 ± 2.39 M for 2, and 21.89 ± 3.19 M for 3. Antitumor mechanism studies showed that complex 2 can increase the autophagy, reactive oxygen species (ROS) levels, and decrease the mitochondrial membrane potential remarkably in a dose-dependent manner in the Eca-109 cells. Complex 2 can cause cell cycle arrest in the G2/M phase. Additionally, complex 2 can regulate the Bcl-2 family and autophagy-related proteins.
三种六配位八面体镍(II)配合物,[Ni (Trp-sal) (phen) (CHOH)](1)、[Ni (Trp-van) (phen) (CHOH)]•2CHOH(2)和[Ni (Trp-naph) (phen) (CHOH)](3)(其中Trp-sal = 由色氨酸和水杨醛衍生的席夫碱,Trp-van = 由色氨酸和香草醛衍生的席夫碱,Trp-naph = 由色氨酸和2-羟基-1-萘醛衍生的席夫碱,phen = 1,10-菲咯啉)已被合成并表征为潜在的抗癌剂。使用单晶X射线晶体学对这些配合物进行结构研究的详细结果表明,镍(II)离子周围扭曲的八面体环境由三个氮原子和三个氧原子满足。所有这些配合物对食管癌细胞系Eca-109均表现出中等细胞毒性,1的IC值为23.95 ± 2.54 μM,2为18.14 ± 2.39 μM,3为21.89 ± 3.19 μM。抗肿瘤机制研究表明,配合物2可以在Eca-109细胞中以剂量依赖性方式显著增加自噬、活性氧(ROS)水平,并降低线粒体膜电位。配合物2可导致细胞周期停滞在G2/M期。此外,配合物2可以调节Bcl-2家族和自噬相关蛋白。