{"title":"诊断和治疗整合前药:通过Cys/GSH耗竭的动态探针工程增强乳腺癌I型光动力治疗。","authors":"Yongfei Huang, Junping Liang, Wenbo Lu*, Chenzhong Li* and Zhefeng Fan*, ","doi":"10.1021/acs.analchem.5c03328","DOIUrl":null,"url":null,"abstract":"<p >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 (<b>Bpl-<i>O</i>-Cou</b>). Based on the intramolecular rearrangement mechanism and intramolecular cyclization mechanism, <b>Bpl-<i>O</i>-Cou</b> could discriminate the detection of Cys/GSH accompanied by different fluorescence emissions. Under near-infrared laser irradiation, <b>Bpl-<i>O</i>-Cou</b> + Cys/GSH could produce <sup>•</sup>OH and O<sub>2</sub><sup>–•</sup>, leading to 4T1 cell death. In vivo experiments further illustrated the interventional role of <b>Bpl-<i>O</i>-Cou</b> in the PDT process. This study provides a new idea for the design of multifunctional probes for cancer diagnostics and therapeutics.</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"97 31","pages":"17175–17183"},"PeriodicalIF":6.7000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Diagnostic and Therapeutic Integration Prodrug: Dynamic Probe Engineering via Cys/GSH Depletion to Amplify Type I Photodynamic Therapy for Breast Cancer\",\"authors\":\"Yongfei Huang, Junping Liang, Wenbo Lu*, Chenzhong Li* and Zhefeng Fan*, \",\"doi\":\"10.1021/acs.analchem.5c03328\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >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 (<b>Bpl-<i>O</i>-Cou</b>). Based on the intramolecular rearrangement mechanism and intramolecular cyclization mechanism, <b>Bpl-<i>O</i>-Cou</b> could discriminate the detection of Cys/GSH accompanied by different fluorescence emissions. Under near-infrared laser irradiation, <b>Bpl-<i>O</i>-Cou</b> + Cys/GSH could produce <sup>•</sup>OH and O<sub>2</sub><sup>–•</sup>, leading to 4T1 cell death. In vivo experiments further illustrated the interventional role of <b>Bpl-<i>O</i>-Cou</b> in the PDT process. 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引用次数: 0
摘要
癌症是对人类健康的严重威胁,寻找有效的检测和治疗癌症的方法至关重要。诊断整合是一种新的癌症诊断和治疗策略,可以在一次给药中实现肿瘤的局部检测和治疗,并有效减少对正常组织的毒副作用。小分子探针在传感、靶向、成像和治疗等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,在肿瘤治疗中显示出独特的优势。然而,肿瘤区域Cys/GSH的高表达会消耗PDT过程中光敏剂产生的活性氧,降低肿瘤的治疗效果。本研究以肿瘤微环境中高表达的Cys/GSH为激活源,选择苯并吡喃盐和香豆素染料作为荧光团,以醚键和醛基为识别位点,构建近红外激活的Cys/GSH荧光探针(Bpl-O-Cou)。基于分子内重排机制和分子内环化机制,Bpl-O-Cou可以区分检测不同荧光发射的Cys/GSH。在近红外激光照射下,bpl - o - cu + Cys/GSH可产生•OH和O2-•,导致4T1细胞死亡。体内实验进一步说明了Bpl-O-Cou在PDT过程中的介入作用。该研究为癌症诊断和治疗的多功能探针的设计提供了新的思路。
Diagnostic and Therapeutic Integration Prodrug: Dynamic Probe Engineering via Cys/GSH Depletion to Amplify Type I Photodynamic Therapy for Breast Cancer
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 (Bpl-O-Cou). Based on the intramolecular rearrangement mechanism and intramolecular cyclization mechanism, Bpl-O-Cou could discriminate the detection of Cys/GSH accompanied by different fluorescence emissions. Under near-infrared laser irradiation, Bpl-O-Cou + Cys/GSH could produce •OH and O2–•, leading to 4T1 cell death. In vivo experiments further illustrated the interventional role of Bpl-O-Cou in the PDT process. This study provides a new idea for the design of multifunctional probes for cancer diagnostics and therapeutics.
期刊介绍:
Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.