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新型三联吡啶钌(II)配合物作为 I 型/II 型光敏剂通过铁死亡和免疫原性细胞死亡用于抗肿瘤光动力治疗。

Novel tris-bipyridine based Ru(II) complexes as type-I/-II photosensitizers for antitumor photodynamic therapy through ferroptosis and immunogenic cell death.

机构信息

Department of Oncology, Department of Pharmacy, Affiliated Hospital of Nantong University, Nantong 226001, China; School of Pharmacy and Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target, Nantong Key Laboratory of Small Molecular Drug Innovation, Nantong University, Nantong 226001, China.

School of Pharmacy and Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target, Nantong Key Laboratory of Small Molecular Drug Innovation, Nantong University, Nantong 226001, China.

出版信息

Eur J Med Chem. 2024 Dec 5;279:116909. doi: 10.1016/j.ejmech.2024.116909. Epub 2024 Sep 24.

DOI:10.1016/j.ejmech.2024.116909
PMID:39357314
Abstract

Ru(II) complexes have attracted attention as photosensitizers for their promising photodynamic properties. Herein, novel tris-bipyridine based Ru(II) complexes (6a-e) were synthesized by introducing saturated heterocycles to improve photodynamic properties and lipid-water partition coefficients. Among them, 6d demonstrated significant phototoxicity towards three cancer cells, with IC values of 5.66-7.17 μM, exceeding values in dark (ICs > 100 μM). Under hypoxic conditions, 6d maintained excellent photodynamic activity in A549 cells, with PI values exceeding 24, highlighting its potential for highly effective type-I/-II photodynamic therapy by inducing ROS generation, oxidative stress, and mitochondrial damage. Additionally, it induced ferroptosis and immunogenic cell death of A549 cells by regulating the expression of relevant markers. Finally, 6d remarkably inhibited the growth of A549 transplanted tumor growth by 95.4 %. This Ru(II) complex shows great potential for cancer treatment with its potent photodynamic activity and diverse mechanisms of tumor cell death.

摘要

钌(II)配合物因其有前景的光动力特性而被作为光敏剂引起了关注。在此,通过引入饱和杂环来改善光动力性质和脂水分配系数,合成了新型三吡啶基基于钌(II)的配合物(6a-e)。其中,6d 对三种癌细胞表现出显著的光毒性,IC 值为 5.66-7.17 μM,超过暗毒性(ICs > 100 μM)。在缺氧条件下,6d 在 A549 细胞中保持优异的光动力活性,PI 值超过 24,通过诱导 ROS 生成、氧化应激和线粒体损伤,突出了其用于高效的 I 型/-II 型光动力治疗的潜力。此外,它通过调节相关标记物的表达诱导 A549 细胞发生铁死亡和免疫原性细胞死亡。最后,6d 显著抑制 A549 移植瘤生长达 95.4%。该 Ru(II) 配合物具有强大的光动力活性和多种肿瘤细胞死亡机制,显示出在癌症治疗方面的巨大潜力。

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