Ma Wenli, Ge Xingxing, Xu Zhishan, Zhang Shumiao, He Xiangdong, Li JuanJuan, Xia Xiaorong, Chen Xiaobing, Liu Zhe
Institute of Anticancer Agents Development and Theranostic Application, The Key Laboratory of Life-Organic Analysis and Key Laboratory of Pharmaceutical Intermediates and Analysis of Natural Medicine, Department of Chemistry and Chemical Engineering, Qufu Normal University, Qufu 273165, China.
Department of Chemistry and Chemical Engineering, Shandong Normal University, Jinan 250014, China.
ACS Omega. 2019 Sep 3;4(12):15240-15248. doi: 10.1021/acsomega.9b01863. eCollection 2019 Sep 17.
Two rhodamine-modified half-sandwich Ir(III) complexes with the general formula [(Cp)Ir(ĈN) Cl] were synthesized and characterized, where Cp is 1-biphenyl-2,3,4,5-tetramethylcyclopentadienyl (Cp). Both complexes showed potent anticancer activity against A549, HeLa, and HepG2 cancer cells and normal cells, and altered ligands had an effect on proliferation resistance. The complex enters cells through energy dependence, and because of the different ligands, not only could it affect the anticancer ability of the complex but also could affect the degree of complex lysosome targeting, lysosomal damage, and further prove the antiproliferative mechanism of the complex. Excitingly, antimetastatic experiments demonstrated that complex has the ability to block the migration of cancer cells. Furthermore, although the complex did not show a stronger ability to interfere with the coenzyme NAD/NADH pair by transfer hydrogenation, the intracellular reactive oxygen species (ROS) content has shown a marked increase. NF-κB activity is increased by ROS regulation, and the role of ROS-NF-κB signaling pathway further induces apoptosis. Moreover, cell flow experiments also demonstrated that complex blocked the cell cycle in S phase, but the complex did not cause significant changes in the mitochondrial membrane potential.
合成并表征了两种通式为[(Cp)Ir(ĈN)Cl]的罗丹明修饰的半夹心铱(III)配合物,其中Cp为1-联苯基-2,3,4,5-四甲基环戊二烯基(Cp)。两种配合物均对A549、HeLa和HepG2癌细胞及正常细胞显示出强大的抗癌活性,且配体的改变对增殖抗性有影响。该配合物通过能量依赖进入细胞,并且由于配体不同,其不仅会影响配合物的抗癌能力,还会影响配合物的溶酶体靶向程度、溶酶体损伤,并进一步证明了配合物的抗增殖机制。令人兴奋的是,抗转移实验表明配合物具有阻断癌细胞迁移的能力。此外,尽管该配合物通过转移氢化未表现出更强的干扰辅酶NAD/NADH对的能力,但其细胞内活性氧(ROS)含量已显著增加。ROS调节增加了NF-κB活性,且ROS-NF-κB信号通路的作用进一步诱导了细胞凋亡。此外,细胞流式实验还表明配合物将细胞周期阻滞在S期,但该配合物未引起线粒体膜电位的显著变化。