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口腔异质结耦合介入光纤介导的协同治疗直肠原位癌。

Oral Heterojunction Coupling Interventional Optical Fiber Mediates Synergistic Therapy for Orthotopic Rectal Cancer.

机构信息

Academy of Medical Engineering and Translational Medicine, Medical College, Tianjin University, Tianjin, 300072, China.

Department of Radiology, Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital, Tianjin, 300052, China.

出版信息

Small. 2024 Oct;20(43):e2404741. doi: 10.1002/smll.202404741. Epub 2024 Jun 20.

DOI:10.1002/smll.202404741
PMID:39031679
Abstract

Catalytic therapy has shown great potential for clinical application. However, conventional catalytic therapies rely on reactive oxygen species (ROS) as "therapeutic drugs," which have limitations in effectively inhibiting tumor recurrence and metastasis. Here, a biomimetic heterojunction catalyst is developed that can actively target orthotopic rectal cancer after oral administration. The heterojunction catalyst is composed of quatrefoil star-shaped BiVO (BVO) and ZnInS (ZIS) nanosheets through an in situ direct growth technique. Poly-norepinephrine and macrophage membrane coatings afford the biomimetic heterojunction catalyst (BVO/ZIS@M), which has high rectal cancer targeting and retention abilities. The coupled optical fiber intervention technology activates the multicenter coordination of five catalytic reactions of heterojunction catalysts, including two reduction reactions (O→·O and CO→CO) and three oxidation reactions (HO→·OH, GSH→GSSG, and LA→PA). These catalytic reactions not only induce immunogenic death in tumor cells through the efficient generation of ROS/CO and the consumption of GSH but also specifically lead to the use of lactic acid (LA) as an electron donor to improve catalytic activity and disrupt the LA-mediated immunosuppressive microenvironment, mediating synergistic catalysis and immunotherapy for orthotopic rectal cancer. Therefore, this optical fiber intervention triggered the combination of heterojunction catalytic therapy and immunotherapy, which exhibits prominent antitumor effects.

摘要

催化疗法在临床应用中显示出巨大的潜力。然而,传统的催化疗法依赖于活性氧(ROS)作为“治疗药物”,在有效抑制肿瘤复发和转移方面存在局限性。在这里,开发了一种仿生异质结催化剂,它可以在口服后主动靶向原位直肠癌细胞。该异质结催化剂是通过原位直接生长技术由四叶草星形 BiVO(BVO)和 ZnInS(ZIS)纳米片组成。聚去甲肾上腺素和巨噬细胞膜涂层为仿生异质结催化剂(BVO/ZIS@M)提供了高直肠癌细胞靶向性和保留能力。光纤介入技术激活了异质结催化剂的五个催化反应的多中心协同作用,包括两个还原反应(O→·O 和 CO→CO)和三个氧化反应(HO→·OH、GSH→GSSG 和 LA→PA)。这些催化反应不仅通过高效产生 ROS/CO 和消耗 GSH 诱导肿瘤细胞免疫原性死亡,还特异性地导致乳酸(LA)作为电子供体的利用,以提高催化活性并破坏 LA 介导的免疫抑制微环境,介导协同催化和免疫治疗原位直肠癌细胞。因此,这种光纤干预触发了异质结催化疗法和免疫疗法的结合,表现出突出的抗肿瘤效果。

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