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超声增强型肝细胞癌治疗和肺转移抑制的超小 Enzyodynamic PANoptosis 纳米诱导剂。

Ultrasmall Enzyodynamic PANoptosis Nano-Inducers for Ultrasound-Amplified Hepatocellular Carcinoma Therapy and Lung Metastasis Inhibition.

机构信息

Department of Ultrasound, Affiliated Hospital of Southwest Jiaotong University, The Third People's Hospital of Chengdu, Chengdu, Sichuan, 610031, China.

Department of Gastroenterology, Affiliated Hospital of Southwest Jiaotong University, The Third People's Hospital of Chengdu, Chengdu, Sichuan, 610031, China.

出版信息

Adv Mater. 2024 Nov;36(45):e2409618. doi: 10.1002/adma.202409618. Epub 2024 Sep 3.

Abstract

Addressing the inefficiency of current therapeutic approaches for hepatocellular carcinoma is an urgent and pressing challenge. PANoptosis, a form of inflammatory programmed cell death, presents a dependable strategy for combating cancer by engaging multiple cell death pathways (apoptosis, pyroptosis, and necroptosis). In this study, an ultrasmall BiSnO nanozyme with ultrasound-magnified multienzyme-mimicking properties is designed and engineered as a PANoptosis inducer through destroying the mitochondrial function of tumor cells and enhancing the intracellular accumulation of toxic reactive oxygen species, finally triggering the activation of PANoptosis process. The role of PANoptosis inducer has been verified by the expression of related proteins, including cleaved Caspase 3, NLRP3, N-GSDMD, cleaved Caspase 1, p-MLKL, and RIPK3. The inclusion of external ultrasonic irradiation significantly augments the enzyodynamic therapeutic efficiency. In vitro and in vivo antineoplastic efficacy, along with inhibition of lung metastasis, validate the benefits of the BiSnO-mediated PANoptosis pathway. This study not only elucidates the intricate mechanisms underlying BiSnO as a PANoptosis inducer, but also offers a novel perspective for the treatment of hepatocellular carcinoma.

摘要

解决肝细胞癌当前治疗方法效率低下的问题是一项紧迫而紧迫的挑战。PANoptosis 是一种炎症程序性细胞死亡形式,通过参与多种细胞死亡途径(细胞凋亡、细胞焦亡和坏死性凋亡),提供了一种可靠的抗癌策略。在本研究中,设计并工程化了一种具有超声放大的多酶模拟特性的超小 BiSnO 纳米酶,作为 PANoptosis 诱导剂,通过破坏肿瘤细胞的线粒体功能和增强细胞内毒性活性氧的积累,最终触发 PANoptosis 过程的激活。通过相关蛋白的表达,包括 cleaved Caspase 3、NLRP3、N-GSDMD、cleaved Caspase 1、p-MLKL 和 RIPK3,验证了 PANoptosis 诱导剂的作用。外加超声辐射的加入显著提高了酶动力学治疗效率。体外和体内抗肿瘤疗效以及对肺转移的抑制作用验证了 BiSnO 介导的 PANoptosis 途径的益处。本研究不仅阐明了 BiSnO 作为 PANoptosis 诱导剂的复杂机制,还为肝细胞癌的治疗提供了新的视角。

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