School of Pharmacy, Guangdong Medical University, Dongguan, 523808, China.
Department of Pharmacy, Dongguan People's Hospital, Dongguan, 523059, China.
J Biol Inorg Chem. 2020 Dec;25(8):1107-1116. doi: 10.1007/s00775-020-01827-7. Epub 2020 Oct 20.
As the "powerhouse" of a cell, mitochondria maintain energy homeostasis, synthesize ATP via oxidative phosphorylation, generate ROS signaling molecules, and modulate cell apoptosis. Herein, three Re(I) complexes bearing guanidinium derivatives have been synthesized and characterized. All of these complexes exhibit moderate anticancer activity in HepG2, HeLa, MCF-7, and A549 cancer cells. Mechanism studies indicate that complex 3, Re(CO)3(L)(Im), can selectively localize in the mitochondria and induce cancer cell death through mitochondria-associated pathways. In addition, complex 3 can effectively depress the ability of cell migration, cell invasion, and colony formation.
线粒体作为细胞的“动力源”,维持着能量的动态平衡,通过氧化磷酸化合成 ATP,产生 ROS 信号分子,并调节细胞凋亡。本文合成并表征了三个含有胍基衍生物的 Re(I) 配合物。这些配合物在 HepG2、HeLa、MCF-7 和 A549 癌细胞中均表现出中等的抗癌活性。机制研究表明,配合物 3,[Re(CO)3(L)(Im)] (PF),可以选择性地定位于线粒体,并通过线粒体相关途径诱导癌细胞死亡。此外,配合物 3 可以有效地抑制细胞迁移、侵袭和集落形成的能力。