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用于通过凋亡和坏死进行抗缺氧肿瘤光动力治疗的新型单光子/双光子激发β-咔啉/喹啉鎓光敏剂。

Novel one-/two-photon excited β-carboline/quinolinium photosensitizers for hypoxia-resistant tumor photodynamic therapy through apoptosis and necrosis.

作者信息

Ji Dongliang, Chen Jian, Ma Yifan, Jiang Yangyang, Xu Ke, Yuan Zifei, Ling Yong, Yang Tao, Zhang Yanan

机构信息

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

Department of Pharmacy, Affiliated Hospital of Nantong University. Nantong 226001, Jiangsu, PR China.

出版信息

Bioorg Chem. 2025 Jul 1;161:108538. doi: 10.1016/j.bioorg.2025.108538. Epub 2025 Apr 26.

Abstract

Photodynamic therapy (PDT) represents an innovative modality that employs photosensitizer for the treatment of tumors, dermatological conditions, and vascular disorders. Herein, a series of novel photosensitizers 2a-e were designed and synthesized by incorporating quinolinium into the β-carboline. In particular, photosensitizer 2d generated a large amount of type-I/-II active oxygen species, including O, •O, and •OH under one-/two-photon excitation. Furthermore, 2d effectively overcame the tumor hypoxic microenvironment and exhibited strong one-/two-photon photodynamic activities against HT29 cells (ICs = 0.18-0.56 μM, PIs = 88-263). Additionally, 2d could significantly induce cancer cell apoptosis via reducing Bcl-2 and increasing Bax/Cleaved-caspase-3, and simultaneously promote programmed necrosis through boosting P-MLKL and P-RIPK1/3 expression. In vivo experiments substantiated that 2d powerfully suppressed colonic tumor growth under one-/two-photon irradiation (suppression rates 77-91 %). Therefore, this work may provide an effective approach for designing novel β-carboline/quinolinium photosensitizers and present a promising prospect in the field of one-/two-photon tumor photodynamic therapy.

摘要

光动力疗法(PDT)是一种创新的治疗方式,它利用光敏剂来治疗肿瘤、皮肤病和血管疾病。在此,通过将喹啉鎓引入β-咔啉,设计并合成了一系列新型光敏剂2a - e。特别地,光敏剂2d在单光子/双光子激发下产生大量的I型/II型活性氧,包括O、•O和•OH。此外,2d有效地克服了肿瘤缺氧微环境,并对HT29细胞表现出强烈的单光子/双光子光动力活性(IC50 = 0.18 - 0.56 μM,PI = 88 - 263)。此外,2d可通过降低Bcl-2和增加Bax/裂解的caspase-3显著诱导癌细胞凋亡,同时通过增强P-MLKL和P-RIPK1/3表达促进程序性坏死。体内实验证实,2d在单光子/双光子照射下能有效抑制结肠肿瘤生长(抑制率77 - 91%)。因此,这项工作可能为设计新型β-咔啉/喹啉鎓光敏剂提供一种有效方法,并在单光子/双光子肿瘤光动力治疗领域展现出广阔前景。

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