Anhui Key Laboratory of Functional Coordination Compounds, School of Chemistry and Chemical Engineering, Anqing Normal University, Anqing, 246011, China; Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing, 210023, China.
Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing, 210023, China.
J Inorg Biochem. 2020 Sep;210:111132. doi: 10.1016/j.jinorgbio.2020.111132. Epub 2020 Jun 10.
Polypyridyl ruthenium complexes as novel photosensitizers had drawn attention due to its high selectivity towards cancer cells and low toxicity to normal cells. Herein, we synthesized a lysosome-targeted polypyridyl ruthenium complex Rhein-Ru(bpy) (bpy = 2,2'-bipyridine, rhein = 4,5-dihydroxy-9,10-dioxoanthracene-2-carboxylic acid), tethering with the Chinese medicine herb rhein. Rhein-Ru(bpy) exhibited high phototoxicity with short time of irradiation against tumor cell lines with the IC value of 2.4- 8.7 μM, and higher cytotoxicity against cisplatin-resistant A2780 cell lines, suggesting that Rhein-Ru(bpy) could overcome the cisplatin resistance. Moreover, Rhein-Ru(bpy) displayed low cytotoxicity towards cell lines in dark incubation, which was beneficial to reduce the toxic side effects towards normal cell lines. Besides, the confocal imaging and western blotting assay results suggested that Rhein-Ru(bpy) could induce cancer cell death through the autophagy pathway. These results inspired us that lysosome-targeted photosensitizers based on ruthenium complexes showed great potential for photodynamic therapy (PDT) application in cancer treatment.
基于聚吡啶钌配合物的新型光动力治疗剂因其对癌细胞的高选择性和对正常细胞的低毒性而受到关注。本研究合成了一种溶酶体靶向聚吡啶钌配合物 Rhein-Ru(bpy)(bpy=2,2'-联吡啶,rheine=4,5-二羟基-9,10-二氧代蒽-2-羧酸),它与中药大黄酸相连。Rhein-Ru(bpy) 对肿瘤细胞系具有高的光毒性,在短时间的照射下即可达到 2.4-8.7 μM 的 IC 值,对顺铂耐药的 A2780 细胞系的细胞毒性更高,提示 Rhein-Ru(bpy) 可以克服顺铂耐药性。此外,Rhein-Ru(bpy) 在黑暗孵育时对细胞系的细胞毒性较低,这有利于减少对正常细胞系的毒性副作用。此外,共聚焦成像和 Western blot 检测结果表明,Rhein-Ru(bpy) 可以通过自噬途径诱导癌细胞死亡。这些结果启发我们,基于钌配合物的溶酶体靶向光动力治疗剂在癌症治疗的光动力治疗(PDT)应用中具有巨大的潜力。