Tumor Site‐Specific In Vivo Theranostics Enabled by Microenvironment‐Dependent Chemical Transformation and Self‐Amplifying Effect

Abstract Precise tumor diagnosis and treatment remain complex challenges. While numerous fluorescent probes have been developed for tumor‐specific imaging and therapy, few exhibit effective function in vivo. Herein, a probe called TQ‐H2 is designed that can realize robust theranostic effects both in...

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Main Authors: Yunfei Zuo, Pei Li, Wen‐Jin Wang, Changhuo Xu, Shuting Xu, Herman H. Y. Sung, Jianwei Sun, Guorui Jin, Weiping Wang, Ryan T. K. Kwok, Jacky W. Y. Lam, Ben Zhong Tang
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Advanced Science
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Online Access:https://doi.org/10.1002/advs.202409506
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author Yunfei Zuo
Pei Li
Wen‐Jin Wang
Changhuo Xu
Shuting Xu
Herman H. Y. Sung
Jianwei Sun
Guorui Jin
Weiping Wang
Ryan T. K. Kwok
Jacky W. Y. Lam
Ben Zhong Tang
author_facet Yunfei Zuo
Pei Li
Wen‐Jin Wang
Changhuo Xu
Shuting Xu
Herman H. Y. Sung
Jianwei Sun
Guorui Jin
Weiping Wang
Ryan T. K. Kwok
Jacky W. Y. Lam
Ben Zhong Tang
author_sort Yunfei Zuo
collection DOAJ
description Abstract Precise tumor diagnosis and treatment remain complex challenges. While numerous fluorescent probes have been developed for tumor‐specific imaging and therapy, few exhibit effective function in vivo. Herein, a probe called TQ‐H2 is designed that can realize robust theranostic effects both in vitro and in vivo. In vitro, TQ‐H2 specifically targets the lysosome and reacts with hydroxyl radical (·OH) to generate TQ‐HA, which lights up the cells. TQ‐HA generates reactive oxygen species (ROS) under light irradiation, enabling the simultaneous induction and monitoring of apoptosis and ferroptosis in tumor cells. Remarkably, TQ‐HA also acts as a self‐amplifier, autocatalytically activating TQ‐H2 by generating ·OH under light exposure. This self‐amplification aligns with the tumor microenvironment, where TQ‐H2 undergoes chemical transformation, distinguishing tumors from healthy tissue via near‐infrared (NIR) fluorescence imaging. Furthermore, ROS generated by TQ‐HA effectively kills tumor cells and inhibits tumor growth without harming normal cells. This study offers a promising strategy for targeted tumor theranostics using self‐amplifying microenvironment‐responsive fluorescent probes.
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spelling doaj-art-bd0377b9fd8a48b3806044f8f73f4ca72025-01-29T09:50:18ZengWileyAdvanced Science2198-38442025-01-01124n/an/a10.1002/advs.202409506Tumor Site‐Specific In Vivo Theranostics Enabled by Microenvironment‐Dependent Chemical Transformation and Self‐Amplifying EffectYunfei Zuo0Pei Li1Wen‐Jin Wang2Changhuo Xu3Shuting Xu4Herman H. Y. Sung5Jianwei Sun6Guorui Jin7Weiping Wang8Ryan T. K. Kwok9Jacky W. Y. Lam10Ben Zhong Tang11Department of Chemistry Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Division of Life Science State Key Laboratory of Molecular Neuroscience and Department of Chemical and Biological Engineering The Hong Kong University of Science & Technology Clear Water Bay Kowloon Hong Kong 999077 P. R. ChinaDepartment of Chemistry Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Division of Life Science State Key Laboratory of Molecular Neuroscience and Department of Chemical and Biological Engineering The Hong Kong University of Science & Technology Clear Water Bay Kowloon Hong Kong 999077 P. R. ChinaChina Clinical Translational Research Center of Aggregation‐Induced Emission The Second Affiliated Hospital School of Medicine School of Science and Engineering Shenzhen Institute of Aggregate Science and Technology The Chinese University of Hong Kong Shenzhen (CUHK‐Shenzhen) Guangdong 518172 ChinaMOE Frontiers Science Center for Precision Oncology Faculty of Health Sciences University of Macau Macao 999078 ChinaDepartment of Pharmacology and Pharmacy Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong 999077 ChinaDepartment of Chemistry Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Division of Life Science State Key Laboratory of Molecular Neuroscience and Department of Chemical and Biological Engineering The Hong Kong University of Science & Technology Clear Water Bay Kowloon Hong Kong 999077 P. R. ChinaDepartment of Chemistry Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Division of Life Science State Key Laboratory of Molecular Neuroscience and Department of Chemical and Biological Engineering The Hong Kong University of Science & Technology Clear Water Bay Kowloon Hong Kong 999077 P. R. ChinaThe Key Laboratory of Biomedical Information Engineering of Ministry of Education School of Life Science and Technology Xi'an Jiaotong University Xi'an 710049 ChinaDepartment of Pharmacology and Pharmacy Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong 999077 ChinaDepartment of Chemistry Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Division of Life Science State Key Laboratory of Molecular Neuroscience and Department of Chemical and Biological Engineering The Hong Kong University of Science & Technology Clear Water Bay Kowloon Hong Kong 999077 P. R. ChinaDepartment of Chemistry Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Division of Life Science State Key Laboratory of Molecular Neuroscience and Department of Chemical and Biological Engineering The Hong Kong University of Science & Technology Clear Water Bay Kowloon Hong Kong 999077 P. R. ChinaDepartment of Chemistry Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Division of Life Science State Key Laboratory of Molecular Neuroscience and Department of Chemical and Biological Engineering The Hong Kong University of Science & Technology Clear Water Bay Kowloon Hong Kong 999077 P. R. ChinaAbstract Precise tumor diagnosis and treatment remain complex challenges. While numerous fluorescent probes have been developed for tumor‐specific imaging and therapy, few exhibit effective function in vivo. Herein, a probe called TQ‐H2 is designed that can realize robust theranostic effects both in vitro and in vivo. In vitro, TQ‐H2 specifically targets the lysosome and reacts with hydroxyl radical (·OH) to generate TQ‐HA, which lights up the cells. TQ‐HA generates reactive oxygen species (ROS) under light irradiation, enabling the simultaneous induction and monitoring of apoptosis and ferroptosis in tumor cells. Remarkably, TQ‐HA also acts as a self‐amplifier, autocatalytically activating TQ‐H2 by generating ·OH under light exposure. This self‐amplification aligns with the tumor microenvironment, where TQ‐H2 undergoes chemical transformation, distinguishing tumors from healthy tissue via near‐infrared (NIR) fluorescence imaging. Furthermore, ROS generated by TQ‐HA effectively kills tumor cells and inhibits tumor growth without harming normal cells. This study offers a promising strategy for targeted tumor theranostics using self‐amplifying microenvironment‐responsive fluorescent probes.https://doi.org/10.1002/advs.202409506aggregation‐induced emissionautocatalytic reactioncancer theranosticshydroxyl radical probesspecific targeting
spellingShingle Yunfei Zuo
Pei Li
Wen‐Jin Wang
Changhuo Xu
Shuting Xu
Herman H. Y. Sung
Jianwei Sun
Guorui Jin
Weiping Wang
Ryan T. K. Kwok
Jacky W. Y. Lam
Ben Zhong Tang
Tumor Site‐Specific In Vivo Theranostics Enabled by Microenvironment‐Dependent Chemical Transformation and Self‐Amplifying Effect
Advanced Science
aggregation‐induced emission
autocatalytic reaction
cancer theranostics
hydroxyl radical probes
specific targeting
title Tumor Site‐Specific In Vivo Theranostics Enabled by Microenvironment‐Dependent Chemical Transformation and Self‐Amplifying Effect
title_full Tumor Site‐Specific In Vivo Theranostics Enabled by Microenvironment‐Dependent Chemical Transformation and Self‐Amplifying Effect
title_fullStr Tumor Site‐Specific In Vivo Theranostics Enabled by Microenvironment‐Dependent Chemical Transformation and Self‐Amplifying Effect
title_full_unstemmed Tumor Site‐Specific In Vivo Theranostics Enabled by Microenvironment‐Dependent Chemical Transformation and Self‐Amplifying Effect
title_short Tumor Site‐Specific In Vivo Theranostics Enabled by Microenvironment‐Dependent Chemical Transformation and Self‐Amplifying Effect
title_sort tumor site specific in vivo theranostics enabled by microenvironment dependent chemical transformation and self amplifying effect
topic aggregation‐induced emission
autocatalytic reaction
cancer theranostics
hydroxyl radical probes
specific targeting
url https://doi.org/10.1002/advs.202409506
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