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利用纳米颗粒工程化细菌和仿生细菌衍生物用于癌症治疗。

Engineering Bacteria and Bionic Bacterial Derivatives with Nanoparticles for Cancer Therapy.

机构信息

Guangdong Key Laboratory of Research and Development of Natural Drugs, and School of Pharmacy, Guangdong Medical University, Dongguan, 523808, P. R. China.

Marshall Laboratory of Biomedical Engineering, International Cancer Center, Laboratory of Evolutionary Theranostics, School of Biomedical Engineering, Shenzhen University Health Science Center, Shenzhen, 518060, P. R. China.

出版信息

Small. 2022 Mar;18(12):e2104643. doi: 10.1002/smll.202104643. Epub 2021 Dec 15.

Abstract

Natural bacteria are interesting subjects for cancer treatments owing to their unique autonomy-driven and hypoxic target properties. Genetically modified bacteria (such as bacteria with msbB gene and aroA gene modifications) can effectively cross sophisticated physiological barriers and transport antitumor agents into deep tumor tissues, and they have good biosafety. Additionally, bacteria can secrete cytokines (such as interleukin-224, interferon-gamma [IFN-γ], and interleukin-1β) and activate antitumor immune responses in the tumor microenvironment, resulting in tumor inhibition. All of these characteristics can be easily utilized to develop synergistic antitumor strategies by combining bacteria-based agents with other therapeutic approaches. Herein, representative studies of bacteria-instructed multimodal synergistic cancer therapy are introduced (e.g., photothermal therapy, chemoimmunotherapy, photodynamic therapy, and photocontrolled bacterial metabolite therapy), and their key advantages are systematically expounded. The current challenges and future prospects in advancing the development of bacteria-based micro/nanomedicines in the field of synthetic biology research are also emphasized, which will hopefully promote the development of related bacteria-based cancer therapies.

摘要

天然细菌因其独特的自主驱动和缺氧靶向特性,成为癌症治疗的有趣对象。经过基因改造的细菌(如 msbB 基因和 aroA 基因修饰的细菌)可以有效地穿越复杂的生理屏障,并将抗肿瘤药物输送到深部肿瘤组织中,具有良好的生物安全性。此外,细菌可以分泌细胞因子(如白细胞介素-224、干扰素-γ[IFN-γ]和白细胞介素-1β),并在肿瘤微环境中激活抗肿瘤免疫反应,从而抑制肿瘤。所有这些特性都可以很容易地被利用,通过将基于细菌的药物与其他治疗方法相结合,来开发协同抗肿瘤策略。本文介绍了几种基于细菌的多模式协同癌症治疗的代表性研究(如光热疗法、化疗免疫疗法、光动力疗法和光控细菌代谢产物疗法),并系统地阐述了它们的关键优势。还强调了在推进合成生物学研究领域基于细菌的微/纳米药物发展方面的当前挑战和未来前景,这有望促进相关的基于细菌的癌症治疗的发展。

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