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Mitochondria-Targeting AIEgens as Pyroptosis Inducers for Boosting Type-I Photodynamic Therapy of Tongue Squamous Cell Carcinoma

Ying Peng, Rufan Mo, Mingwang Yang, Huilin Xie, Fulong Ma, Zeyang Ding, Song Wu, Jacky W. Y. Lam, Juan Du, Jianquan Zhang, Zheng Zhao, Ben Zhong Tang

2024ACS Nano30 citationsDOI

Abstract

The development of a photosensitizer (PS) that induces pyroptosis could be a star for photodynamic therapy (PDT), particularly with type-I PSs that produce reactive oxygen species (ROS) in a hypoxic tumor microenvironment. Since pyroptosis is a recently characterized cell death pathway, it holds promise for advancing PDT in oncology, with PSs playing a critical role. Herein, we develop a PS named Th-M with aggregation-induced emission (AIE) characteristics for type-I PDT against tongue squamous cell carcinoma (TSCC). Th-M stands out for its exceptional mitochondrial-targeting ability, which triggers mitochondrial dysfunction and leads to Caspase-3 and Gasdermin E (GSDME) cleavage under white light irradiation, inducing pyroptosis in TSCC cells. Our studies verify the effectiveness of Th-M in destroying cancer cells in vitro and suppressing tumor growth in vivo while also demonstrating a favorable biosafety profile. This work pioneers the application of Th-M as a mitochondria-targeted, type-I PS that leverages the mechanism of pyroptosis, offering a potent approach for the treatment of TSSC with promising implications for future PDT of cancers.

Topics & Concepts

Photodynamic therapyPyroptosisCancer researchBasal cellPhotosensitizerTongueBoosting (machine learning)Materials scienceMedicineChemistryApoptosisProgrammed cell deathPhotochemistryPathologyBiochemistryComputer scienceMachine learningOrganic chemistryNanoplatforms for cancer theranosticsHeme Oxygenase-1 and Carbon MonoxidePhotodynamic Therapy Research Studies