Ji Dongliang, Chen Jian, Ma Yifan, Jiang Yangyang, Xu Ke, Yuan Zifei, Ling Yong, Yang Tao, Zhang Yanan
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.
Bioorg Chem. 2025 Jul 1;161:108538. doi: 10.1016/j.bioorg.2025.108538. Epub 2025 Apr 26.
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.
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。