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用于癌症治疗药物近红外光诱导表达的工程菌。

Engineered bacteria for near-infrared light-inducible expression of cancer therapeutics.

作者信息

Qiao Longliang, Niu Lingxue, Wang Zhihao, Deng Zhenqiang, Di Dai, Ma Xiaoding, Zhou Yang, Kong Deqiang, Wang Qilin, Yin Jianli, Jin Lingli, Sun Jing, Feng Bo, Lu Weiqiang, Cai Fengfeng, Guan Ningzi, Ye Haifeng

机构信息

Shanghai Frontiers Science Center of Genome Editing and Cell Therapy, Biomedical Synthetic Biology Research Center, Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, Shanghai Academy of Natural Sciences (SANS), East China Normal University, Shanghai, China.

Department of Breast Surgery, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.

出版信息

Nat Cancer. 2025 Apr;6(4):612-628. doi: 10.1038/s43018-025-00932-3. Epub 2025 Mar 17.

Abstract

Bacteria-based therapies hold great promise for cancer treatment due to their selective tumor colonization and proliferation. However, clinical application is hindered by the need for safe, precise control systems to regulate local therapeutic payload expression and release. Here we developed a near-infrared (NIR) light-mediated PadC-based photoswitch (NETMAP) system based on a chimeric phytochrome-activated diguanylyl cyclase (PadC) and a cyclic diguanylate monophosphate-dependent transcriptional activator (MrkH). The NETMAP-engineered bacteria exhibited antitumor performance in mouse tumor models with different levels of immunogenicity. Specifically, in immunogenic lymphoma tumors, NIR-induced PD-L1 and CTLA-4 nanobodies enhanced the activation of adaptive immunity. In low-immunogenic tumors-including mouse-derived colon cancer models, an orthotopic human breast cancer cell line-derived xenograft model and a colorectal cancer patient-derived xenograft model-NIR-induced azurin and cytolysin A predominantly led to tumor inhibition. Our study identifies an NIR light-mediated therapeutic platform for engineered bacteria-based therapies with customizable outputs and precise dosage control.

摘要

基于细菌的疗法因其能够选择性地在肿瘤中定殖和增殖,在癌症治疗方面具有巨大潜力。然而,临床应用受到阻碍,因为需要安全、精确的控制系统来调节局部治疗载荷的表达和释放。在此,我们基于嵌合光敏色素激活的二鸟苷酸环化酶(PadC)和环二鸟苷单磷酸依赖性转录激活因子(MrkH),开发了一种近红外(NIR)光介导的基于PadC的光开关(NETMAP)系统。NETMAP工程菌在具有不同免疫原性水平的小鼠肿瘤模型中表现出抗肿瘤性能。具体而言,在免疫原性淋巴瘤肿瘤中,近红外诱导的PD-L1和CTLA-4纳米抗体增强了适应性免疫的激活。在低免疫原性肿瘤中,包括小鼠源结肠癌模型、原位人乳腺癌细胞系衍生的异种移植模型和结直肠癌患者衍生的异种移植模型,近红外诱导的蓝铜蛋白和溶细胞素A主要导致肿瘤抑制。我们的研究确定了一种近红外光介导的治疗平台,用于基于工程菌的疗法,具有可定制的输出和精确的剂量控制。

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