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通过膜锚定 AIE 光敏剂设计激活细胞焦亡:光动力癌症细胞消融的新展望。

Activation of Pyroptosis by Membrane-Anchoring AIE Photosensitizer Design: New Prospect for Photodynamic Cancer Cell Ablation.

机构信息

Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore, 117585, Singapore.

Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou, 350207, China.

出版信息

Angew Chem Int Ed Engl. 2021 Apr 12;60(16):9093-9098. doi: 10.1002/anie.202016399. Epub 2021 Mar 8.

Abstract

Pyroptosis as a lytic and inflammatory form of cell death is a powerful tool to fight against cancer. However, pyroptosis is usually activated by chemotherapeutic drugs, which limits its anti-tumor applications due to drug resistance and severe side effects. Herein, we demonstrate that membrane targeting photosensitizers can induce pyroptosis for cancer cell ablation with noninvasiveness and low side effects. A series of membrane anchoring photosensitizers (TBD-R PSs) with aggregation-induced emission (AIE) characteristics were prepared through conjugation of TBD and phenyl ring with cationic chains. Upon light irradiation, cytotoxic ROS were produced in situ, resulting in direct membrane damage and superior cancer cell ablation. Detailed study revealed that pyroptosis gradually became the dominant cell death pathway along with the increase of TBD-R PSs membrane anchoring capability. This study offers a photo-activated pyroptosis-based intervention strategy for cancer cell ablation.

摘要

细胞焦亡作为一种裂解性和炎症性的细胞死亡形式,是对抗癌症的有力工具。然而,细胞焦亡通常是由化疗药物激活的,由于耐药性和严重的副作用,这限制了其在抗肿瘤中的应用。在此,我们证明了膜靶向光敏剂可以通过非侵入性和低副作用诱导细胞焦亡来消融癌细胞。通过将 TBD 与带有正电荷的链的苯环连接,制备了一系列具有聚集诱导发射(AIE)特性的膜锚定光敏剂(TBD-R PSs)。光照后,原位产生细胞毒性 ROS,导致直接的膜损伤和优异的癌细胞消融效果。详细研究表明,随着 TBD-R PSs 膜锚定能力的增加,细胞焦亡逐渐成为主要的细胞死亡途径。本研究为癌症细胞消融提供了一种基于光激活细胞焦亡的干预策略。

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