An ER‐targeted, Viscosity‐sensitive Hemicyanine Dye for the Diagnosis of Nonalcoholic Fatty Liver and Photodynamic Cancer Therapy by Activating Pyroptosis Pathway

Author:

Zeng Shuang12,Wang Yang1,Chen Chen2,Kim Heejeong3,Liu Xiaosheng2,Jiang Maojun1,Yu Yichu2,Kafuti Yves S.2,Chen Qixian2,Wang Jingyun12,Peng Xiaojun1,Li Haidong124,Yoon Juyoung3ORCID

Affiliation:

1. State Key Laboratory of Fine Chemicals Dalian University of Technology 2 Linggong Road, Hi-tech Zone 116024 Dalian China

2. MOE Key Laboratory of Bio-Intelligent Manufacturing School of Bioengineering Dalian University of Technology 2 Linggong Road, Hi-tech Zone 116024 Dalian China

3. Department of Chemistry and Nanoscience Ewha Womans University 03760 Seoul Korea

4. Provincial Key Laboratory of Interdisciplinary Medical Engineering for Gastrointestinal Carcinoma Cancer Hospital of Dalian University of Technology Liaoning Cancer Hospital & Institute) 110042 Shenyang, Liaoning China

Abstract

AbstractThe concept of molecular design, integrating diagnostic and therapeutic functions, aligns with the general trend of modern medical advancement. Herein, we rationally designed the smart molecule ER‐ZS for endoplasmic reticulum (ER)‐targeted diagnosis and treatment in cell and animal models by combining hemicyanine dyes with ER‐targeted functional groups (p‐toluenesulfonamide). Owing to its ability to target the ER with a highly specific response to viscosity, ER‐ZS demonstrated substantial fluorescence turn‐on only after binding to the ER, independent of other physiological environments. In addition, ER‐ZS, being a small molecule, allows for the diagnosis of nonalcoholic fatty liver disease (NAFLD) via liver imaging based on high ER stress. Importantly, ER‐ZS is a type I photosensitizer, producing O2 and ⋅OH under light irradiation. Thus, after irradiating for a certain period, the photodynamic therapy inflicted severe oxidative damage to the ER of tumor cells in hypoxic (2 % O2) conditions and activated the unique pyroptosis pathway, demonstrating excellent antitumor capacity in xenograft tumor models. Hence, the proposed strategy will likely shed new light on integrating molecular optics for NAFLD diagnosis and cancer therapy.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

National Research Foundation of Korea

Publisher

Wiley

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