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合成 Notch (synNotch) 受体在癌症治疗中的工程化策略与治疗应用

英文原题:Engineering strategies and therapeutic applications of synthetic Notch (synNotch) receptors in cancer therapeutics.

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Engineering strategies and therapeutic applications of synthetic Notch (synNotch) receptors in cancer therapeutics.

PubMed 2026/02/09(内容时间) Drug Discov Today Q1 · IF 8.7(JCR 2025)

研究概要

合成 Notch(synNotch)受体已被开发为细胞免疫治疗的一种新方法,并将提供可编程、特异性的癌症治疗。

中文摘要

合成Notch(synNotch)受体作为一种新型细胞免疫疗法策略被开发出来,可提供可编程、特异性的癌症治疗。与现有固定式嵌合抗原受体(CAR)T细胞疗法不同,synNotch受体由胞外、跨膜和胞内等模块化结构域组成,可根据所遇配体影响基因表达。通过基于布尔逻辑的细胞决策,synNotch受体提高了治疗精准度并降低靶外效应。逻辑调控回路利用配体—受体组合,以高度特异方式识别肿瘤微环境指标。临床前模型已显示synNotch在胶质瘤和胰腺癌等实体瘤中的潜力:通过控制CAR表达和调节细胞因子,可能突破免疫抑制生态位及抗原逃逸等障碍。持续发展正在解决工程设计难题;将synNotch与CAR-T或诱导多能干细胞等技术结合,可能成为癌症治疗的变革性策略。

展开英文摘要原文

Synthetic Notch (synNotch) receptors have been developed as a novel approach to cell-based immunotherapy and will provide programmable, specific cancer treatments. Unlike existing fixed chimeric antigen receptor (CAR)-T cell therapies, synNotch receptors are a combination of modular domains, such as extracellular, transmembrane, and intracellular domains, for influencing gene expression depending on the present ligand. Through Boolean logic-based cellular decisions, synNotch receptors allow for a higher degree of precision and a lower degree of off-target effects. Logic-regulated circuits use pairs of ligands and receptors to detect indicators of the tumour microenvironment in a highly specific manner. The potential of synNotch in solid tumours such as glioma and pancreatic cancer has been demonstrated in preclinical models using CAR expression control and the ability to regulate cytokines, a method that could break through the obstacles of immunosuppressive niches and antigen escape. Continuous developments are resolving engineering challenges, and the fusion of synNotch with technologies such as CAR-T or induced pluripotent stem cells could be a transformative approach in cancer therapy.

论文信息

作者
Gholap AD、Vengurlekar JR、Hatvate NT、Thorat ND
第一作者单位
Department of Pharmaceutics, St. John Institute of Pharmacy and Research, Palghar, Maharashtra 401404, India.India
通讯作者单位
Department of Physics, Bernal Institute, and Limerick Digital Cancer Research Centre (LDCRC), University of Limerick, Castletroy, Limerick V94T9PX, Ireland. Electronic address: nanasaheb.d.thorat@ul.ie.Switzerland
文献类型
综述
期刊
Drug discovery today2026 Mar
原文标识
PubMed 41672235 · DOI 10.1016/j.drudis.2026.104619