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微生物介导的光合产氧和铁死亡诱导重塑肿瘤微环境以增强纳米动力学治疗。

Microorganism-enabled photosynthetic oxygeneration and ferroptosis induction reshape tumor microenvironment for augmented nanodynamic therapy.

作者信息

Lu Shuting, Feng Wei, Yao Xijuan, Song Xinran, Guo Jinhe, Chen Yu, Hu Zhongqian

机构信息

Center of Interventional Radiology and Vascular Surgery, Department of Radiology and Ultrasound, Zhongda Hospital, Medical School, Southeast University, Nanjing, 210009, PR China.

Materdicine Lab, School of Life Sciences, Shanghai University, Shanghai, 200444, PR China.

出版信息

Biomaterials. 2022 Aug;287:121688. doi: 10.1016/j.biomaterials.2022.121688. Epub 2022 Jul 21.

Abstract

Nanodynamic therapy (NDT) based on reactive oxygen species (ROS) generation has been envisioned as a distinct modality for efficient cancer treatment. However, insufficient ROS generation and partial ROS consumption frequently limit the theraputic effect and outcome of NDT owing to the low oxygen (O) tension and high glutathione (GSH) level in tumor microenvironment (TME). To circumvent these critical issues, we herein proposed and engineered the biodegradable GSH-depletion Mn(III)-riched manganese oxide nanospikes (MnO NSs) with the photosynthetic bacterial cyanobacteria (Cyan) as a high-efficient and synergistic platform to reshape TME by simultaneously increasing oxygen content and decreasing GSH level. Specifically, under the trigger of acidity, MnO NSs reacted with photosynthetic oxygen can generate toxic singlet oxygen (O). Moreover, MnO NSs significantly reduced intracellular GSH, resulting in decreased GPX4 activity, which induced tumor cell non-apoptotic ferroptosis. Consequently, this combined strategy based on coadministration with Cyan and MnO NSs demonstrated the superior antitumor efficacy via amplification of oxidative stress in 4T1 tumor-bearing mice for the synergetic oxygen-augmented nanodynamic/ferroptosis therapy. This work highlights a facile synergistic micro-/nano-system with the specific capability of reshaping TME to augment the sensitivity and therapeutic efficacy of NDT in solid hypoxic tumor therapy.

摘要

基于活性氧(ROS)生成的纳米动力疗法(NDT)被设想为一种有效的癌症治疗独特方式。然而,由于肿瘤微环境(TME)中低氧(O)张力和高谷胱甘肽(GSH)水平,ROS生成不足和部分ROS消耗经常限制NDT的治疗效果和结果。为了规避这些关键问题,我们在此提出并设计了可生物降解的富含Mn(III)的谷胱甘肽消耗型氧化锰纳米尖刺(MnO NSs),以光合细菌蓝藻(Cyan)作为高效协同平台,通过同时增加氧含量和降低GSH水平来重塑TME。具体而言,在酸度触发下,MnO NSs与光合氧反应可生成有毒的单线态氧(O)。此外,MnO NSs显著降低细胞内GSH,导致GPX4活性降低,从而诱导肿瘤细胞非凋亡铁死亡。因此,这种基于与Cyan和MnO NSs共同给药的联合策略通过在4T1荷瘤小鼠中放大氧化应激,展示了协同氧增强纳米动力/铁死亡疗法的卓越抗肿瘤疗效。这项工作突出了一种简便的协同微/纳米系统,其具有重塑TME的特定能力,以增强NDT在实体缺氧肿瘤治疗中的敏感性和治疗效果。

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