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利用 mRNA 保护纳米笼诱导非凋亡性细胞死亡以提高治疗效果。

Improvement of Therapeutic Effect via Inducing Non-Apoptotic Cell Death Using mRNA-Protection Nanocage.

机构信息

Biomaterial Research Center, Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.

Department of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.

出版信息

Adv Healthc Mater. 2024 Oct;13(27):e2400240. doi: 10.1002/adhm.202400240. Epub 2024 Jul 31.

Abstract

Necroptosis, a cell death mechanism with the characteristics of both apoptosis and necrosis, is proposed as a promising therapeutic approach for cancer therapy. Induction of necroptosis for cancer therapy may be possible through the regulation of the expression of a key factor gene receptor-interacting protein kinase-3 (RIPK3) via in vitro transcription (IVT) mRNA delivery. However, mRNA is susceptible to degradation and has a low delivery efficiency, which highlights the requirement of a proper delivery vehicle for intracellular delivery. Therefore, a new mRNA delivery system based on the nanostructured silica nanoparticles, termed mRNA-protective nanocage (mPN) has been developed. High-efficiency expression of RIPK3 and induction of necroptosis is achieved through delivery of RIPK3 IVT mRNA with mPN in vitro and in vivo models. Importantly, the mPN carrying RIPK3 mRNA distributed locally in tumors upon intravascular injection, and successfully induced necroptosis and immune cell infiltration, a hallmark of necroptosis. the suppression of tumor growth in a murine cancer model, demonstrating the synergistic effect of RIPK3 mRNA- and immune cell-mediated therapy is also observed. These findings suggest the potential for anticancer therapy through necroptosis induction and provide a strategy for the development of mRNA-based nanomedicine.

摘要

细胞程序性坏死(Necroptosis),一种具有凋亡和坏死特征的细胞死亡机制,被提出作为癌症治疗的一种有前途的治疗方法。通过体外转录(IVT)mRNA 递送来调节关键因子受体相互作用蛋白激酶 3(RIPK3)的表达,可能诱导细胞程序性坏死用于癌症治疗。然而,mRNA 易降解且递送效率低,这突出了对适当的递送载体进行细胞内递送的要求。因此,已经开发了一种基于纳米结构二氧化硅纳米粒子的新型 mRNA 递送系统,称为 mRNA 保护纳米笼(mPN)。通过 mPN 在体外和体内模型中递送 RIPK3 IVT mRNA,实现了 RIPK3 的高效表达和细胞程序性坏死的诱导。重要的是,携带 RIPK3 mRNA 的 mPN 在血管内注射后局部分布在肿瘤中,并成功诱导了细胞程序性坏死和免疫细胞浸润,这是细胞程序性坏死的标志。在小鼠癌症模型中观察到肿瘤生长的抑制,表明 RIPK3 mRNA 和免疫细胞介导的治疗的协同作用。这些发现提示通过诱导细胞程序性坏死进行抗癌治疗的潜力,并为基于 mRNA 的纳米医学的发展提供了一种策略。

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