School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, 510006, PR China.
School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, 510006, PR China; Guangdong Cosmetics Engineering & Technology Research Center, Guangzhou, 510006, PR China; Guangdong Engineering Research Center for Lead Compounds & Drug Discovery, Guangzhou, 510006, PR China.
Eur J Med Chem. 2018 Feb 10;145:338-349. doi: 10.1016/j.ejmech.2017.11.091. Epub 2017 Dec 1.
An iridium (III) complex [Ir(ppy)(BDPIP)]PF (Ir-1) was reported to show high anticancer activity and may be used as a potent anticancer drug. In the current study, we designed and synthesized a novel iridium (III) complex and evaluated its potential inhibitory effect on the cancer cell growth in vitro and in vivo. This complex was found to display high cytotoxic activity in vitro and in vivo against A549 cell with a low IC value of 3.6 ± 0.3 μM and inhibiting percentage of tumor growth is 63.84% compared with the control. The complex also exhibited potencies superior to that of cisplatin toward A549 cell in vitro and in vivo. Further studies revealed that the complex can induce apoptosis and autophagy, enhance the ROS level, cause a decrease in the mitochondrial membrane potential and inhibit the cell invasion. Our findings indicated that the complex induced apoptosis in A549 through mitochondria dysfunction and PI3K/AKT/mTOR signaling pathways.
报道称,铱(III)配合物[Ir(ppy)(BDPIP)]PF(Ir-1)具有高抗癌活性,可作为一种有效的抗癌药物。在本研究中,我们设计并合成了一种新型的铱(III)配合物,并评估了其在体外和体内对肺癌 A549 细胞生长的潜在抑制作用。该配合物在体外和体内对 A549 细胞表现出高细胞毒性活性,IC 值低至 3.6±0.3μM,与对照组相比,肿瘤生长抑制率为 63.84%。该配合物对 A549 细胞的体外和体内活性也优于顺铂。进一步的研究表明,该配合物可以诱导细胞凋亡和自噬,增加 ROS 水平,导致线粒体膜电位下降,并抑制细胞侵袭。我们的研究结果表明,该配合物通过线粒体功能障碍和 PI3K/AKT/mTOR 信号通路诱导 A549 细胞凋亡。