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载氧化钙聚多巴胺纳米粒对酸性及缺氧肿瘤微环境的调控

Acidic and hypoxic tumor microenvironment regulation by CaO-loaded polydopamine nanoparticles.

机构信息

Key Laboratory of Spine and Spinal Cord Injury Repair and Regeneration, Ministry of Education, School of Medicine, Tongji Hospital, The Institute for Biomedical Engineering & Nano Science, Tongji University, 389 Xincun Road, Shanghai, 200092, China.

Shanghai Skin Disease Hospital, School of Medicine, Tongji University, Shanghai, 200092, China.

出版信息

J Nanobiotechnology. 2022 Dec 28;20(1):544. doi: 10.1186/s12951-022-01752-8.

Abstract

Hypoxia and high accumulation of lactic acid in the tumor microenvironment provide fertile soil for tumor development, maintenance and metastasis. Herein, we developed a calcium peroxide (CaO)-loaded nanostructure that can play a role of "one stone kill two birds", i.e., acidic and hypoxic tumor microenvironment can be simultaneously regulated by CaO loaded nanostructure. Specifically, CaO-loaded mesoporous polydopamine nanoparticles modified with sodium hyaluronate (denoted as CaO@mPDA-SH) can gradually accumulate in a tumor site. CaO exposed in acidic microenvironment can succeed in consuming the lactic acid with oxygen generation simultaneously, which could remodel the acid and hypoxia tumor microenvironment. More importantly, the relief of hypoxia could further reduce lactate production from the source by down-regulating the hypoxia inducible factor-1α (HIF-1α), which further down-regulated the glycolysis associated enzymes including glycolysis-related glucose transporter 1 (GLUT1) and lactate dehydrogenase A (LDHA). As a result, CaO@mPDA-SH alone without the employment of other therapeutics can dually regulate the tumor hypoxia and lactic acid metabolism, which efficiently represses tumor progression in promoting immune activation, antitumor metastasis, and anti-angiogenesis.

摘要

缺氧和肿瘤微环境中乳酸的高度积累为肿瘤的发展、维持和转移提供了肥沃的土壤。在此,我们开发了一种负载过氧钙(CaO)的纳米结构,可以起到“一石二鸟”的作用,即通过负载 CaO 的纳米结构同时调节酸性和缺氧的肿瘤微环境。具体来说,负载过氧钙的介孔聚多巴胺纳米颗粒修饰透明质酸钠(记为 CaO@mPDA-SH)可以逐渐在肿瘤部位积累。暴露在酸性微环境中的 CaO 可以成功地与氧气生成同时消耗乳酸,从而重塑酸性和缺氧的肿瘤微环境。更重要的是,缺氧的缓解可以通过下调缺氧诱导因子-1α(HIF-1α)进一步从源头上减少乳酸的产生,从而进一步下调糖酵解相关酶,包括糖酵解相关葡萄糖转运蛋白 1(GLUT1)和乳酸脱氢酶 A(LDHA)。结果,CaO@mPDA-SH 无需使用其他治疗方法即可双重调节肿瘤缺氧和乳酸代谢,有效地抑制肿瘤进展,促进免疫激活、抗肿瘤转移和抗血管生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f21a/9798656/4c3d64f7b477/12951_2022_1752_Sch1_HTML.jpg

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