详细信息

Cardiolipin-Targeted NIR-II Fluorophore Causes ?Avalanche Effects? for Re-Engaging Cancer Apoptosis and Inhibiting Metastasis  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Cardiolipin-Targeted NIR-II Fluorophore Causes ?Avalanche Effects? for Re-Engaging Cancer Apoptosis and Inhibiting Metastasis

作者:Bian, Hui[2];Ma, Dandan[2];Pan, Fei[3];Zhang, Xiaodong[1];Xin, Kai[1];Zhang, Xinfu[2];Yang, Youjun[1];Peng, Xiaojun[2];Xiao, Yi[2]

机构:[1]East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab Chem Biol, Shanghai 200237, Peoples R China;[2]Dalian Univ Technol, Frontiers Sci Ctr Smart Mat Oriented Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China;[3]Chinese Acad Agr Sci, Inst Apicultural Res, Beijing 100093, Peoples R China

年份:2022

卷号:144

期号:49

起止页码:22562

外文期刊名:JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

收录:;EI(收录号:20225013226394);WOS:【SCI-EXPANDED(收录号:WOS:000891455900001)】;

基金:? ACKNOWLEDGMENTS The author acknowledges the financial support from the National Natural Science Foundation of China (nos. 22174009, 21901031, and 22078047) , Dalian Science and Technology Innovation Fund (no. 2020JJ25CY014) , Science and Technology Foundation of Liaoning Province (2020-YQ- 08) , and the Fundamental Research Funds for the Central Universities (no. DUT20RC (5) 024 and DUT21YG126) .

语种:英文

外文关键词:Annihilation - Cancer cells - Diseases - Fluorescence - Infrared devices - Mammals - Pathology - Phospholipids - Photodynamic therapy - Tumors

摘要:Restoring innate apoptosis and simultaneously inhibiting metastasis by a molecular drug is an effective cancer therapeutic approach. Herein, a large rigid and V-shaped NIR-II dye, DUT850, is rationally designed for potential cardiolipin (CL) targeted chemo-phototheranostic application. DUT850 displays moderate NIR-II fluorescence, excellent photodynamic therapy (PDT) and photothermal therapy (PTT) performance, and ultrahigh photostability. More importantly, the unique rigid V-shaped backbone, positive charge, and lipophilicity of DUT850 afford its specific recognition and efficient binding to CL; such an interaction of DUT850-CL induced a spectrum of physiological disruptions, including translocation of cytochrome c, Ca2+ overload, reactive oxygen species burst, and ATP depletion, which not only activated cancer cell apoptosis but also inhibited tumor metastasis both in vitro and in vivo. Furthermore, the tight binding of DUT850-CL improves the phototoxicity of DUT850 toward cancer cells (IC50 as low as 90 nM) under safe 808 nm laser irradiation (330 mW cm-2). Upon encapsulation into bovine serum albumin (BSA), DUT850@BSA exerted a synergetic chemo-PDT-PTT effect on the 4T1 tumor mouse model, eventually leading to solid tumor annihilation and metastasis inhibition, which could be followed in real time with the NIR-II fluorescence of DUT850. This work contributed a promising approach for simultaneously re-engaging cancer cell apoptotic networks and activating the anti-metastasis pathway by targeting a pivotal upstream effector, which will bring a medical boon for inhibition of tumor proliferation and metastasis.

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