Huang Yongfei, Liang Junping, Lu Wenbo, Li Chenzhong, Fan Zhefeng
Key Laboratory of Magnetic Molecules and Magnetic Information Materials (Ministry of Education), School of Chemistry and Material Science, Shanxi Normal University, Taiyuan 030032, China.
School of Medicine, The Chinese University of Hong Kong, Shenzhen, Guangdong 518172, China.
Anal Chem. 2025 Aug 12;97(31):17175-17183. doi: 10.1021/acs.analchem.5c03328. Epub 2025 Jul 29.
Cancer is a serious threat to human health, and it is essential to find effective methods for detecting and treating cancer. Diagnostic integration is a new strategy for cancer diagnosis and treatment that enables localized detection and treatment of tumors in a single administration and effectively reduces the toxic side effects on normal tissues. It remains a challenge for small-molecule probes to achieve multifunctionality in sensing, targeting, imaging, and therapy. Photodynamic therapy (PDT), which uses photosensitizers to generate reactive oxygen species under specific wavelengths of light to ablate tumor tissue, has demonstrated unique advantages in tumor treatment. However, the high expression of Cys/GSH in the tumor region will consume the reactive oxygen species generated by photosensitizers during PDT and reduce the therapeutic effect of the tumor. In this study, the highly expressed Cys/GSH in the tumor microenvironment was used as the activation source, and benzopyrylium salt and coumarin dyes were selected as fluorophores, with the ether bond and aldehyde group as recognition sites, to construct a near-infrared-activated Cys/GSH fluorescent probe (). Based on the intramolecular rearrangement mechanism and intramolecular cyclization mechanism, could discriminate the detection of Cys/GSH accompanied by different fluorescence emissions. Under near-infrared laser irradiation, + Cys/GSH could produce OH and O, leading to 4T1 cell death. In vivo experiments further illustrated the interventional role of in the PDT process. This study provides a new idea for the design of multifunctional probes for cancer diagnostics and therapeutics.
癌症是对人类健康的严重威胁,找到有效的癌症检测和治疗方法至关重要。诊断一体化是癌症诊断和治疗的一种新策略,能够在单次给药中实现肿瘤的局部检测和治疗,并有效降低对正常组织的毒副作用。小分子探针要在传感、靶向、成像和治疗方面实现多功能性仍然是一个挑战。光动力疗法(PDT)利用光敏剂在特定波长的光下产生活性氧来消融肿瘤组织,在肿瘤治疗中已显示出独特优势。然而,肿瘤区域中高表达的半胱氨酸/谷胱甘肽(Cys/GSH)会在光动力疗法期间消耗光敏剂产生的活性氧,降低肿瘤的治疗效果。在本研究中,将肿瘤微环境中高表达的Cys/GSH用作激活源,选择苯并吡喃盐和香豆素染料作为荧光团,以醚键和醛基作为识别位点,构建了一种近红外激活的Cys/GSH荧光探针()。基于分子内重排机制和分子内环化机制,能够通过不同的荧光发射鉴别检测Cys/GSH。在近红外激光照射下, + Cys/GSH可产生羟基自由基(OH)和单线态氧(O),导致4T1细胞死亡。体内实验进一步说明了在光动力疗法过程中的干预作用。本研究为癌症诊断和治疗的多功能探针设计提供了新思路。