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生物正交调控代谢平衡促进铁死亡和温和光热治疗。

Bioorthogonal Regulated Metabolic Balance for Promotion of Ferroptosis and Mild Photothermal Therapy.

机构信息

Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, P. R. China.

School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China.

出版信息

ACS Nano. 2024 Oct 15;18(41):28104-28114. doi: 10.1021/acsnano.4c07558. Epub 2024 Oct 7.

Abstract

The nanozyme with NADPH oxidase (NOX)-like activity can promote the consumption of NADPH and the generation of free radicals. In consideration of that the upregulation of glucose-6-phosphate dehydrogenase (G6PD) would accelerate the compensation production of NADPH, for inhibition of G6PD activity, our designed bioorthogonal nanozyme can in situ catalyze pro-DHEA to produce G6PD inhibitor and dehydroepiandrosterone (DHEA) drugs to inhibit G6PD activity. Therefore, the well-defined platform can disrupt NADPH homeostasis, leading to the collapse of the antioxidant defense system in the tumor cells. The enzyme-like activity of PdCuFe is further enhanced when irradiated by NIR-II light. The destruction of NADPH homeostasis can promote ferroptosis and, in turn, facilitate mild photothermal therapy. Our design can realize NADPH depletion and greatly improve the therapeutic effect through metabolic regulation, which may provide inspiration for the design of bioorthogonal catalysis.

摘要

具有 NADPH 氧化酶 (NOX)-样活性的纳米酶可以促进 NADPH 的消耗和自由基的产生。考虑到葡萄糖-6-磷酸脱氢酶 (G6PD) 的上调会加速 NADPH 的补偿产生,为了抑制 G6PD 活性,我们设计的生物正交纳米酶可以原位催化前 DHEA 产生 G6PD 抑制剂和脱氢表雄酮 (DHEA) 药物来抑制 G6PD 活性。因此,这个精确定义的平台可以破坏 NADPH 的动态平衡,导致肿瘤细胞中抗氧化防御系统的崩溃。当受到近红外二区 (NIR-II) 光照射时,PdCuFe 的酶样活性进一步增强。破坏 NADPH 动态平衡可以促进铁死亡,并进而促进温和的光热治疗。我们的设计可以通过代谢调节来实现 NADPH 的耗竭,并大大提高治疗效果,这可能为生物正交催化的设计提供灵感。

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