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用于癌症干细胞富集肿瘤检测和治疗的自组装醛脱氢酶激活型纳米前药。

Self-assembled aldehyde dehydrogenase-activatable nano-prodrug for cancer stem cell-enriched tumor detection and treatment.

机构信息

Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore, 117585, Singapore.

College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, 310058, China.

出版信息

Nat Commun. 2024 Oct 31;15(1):9417. doi: 10.1038/s41467-024-53771-8.

Abstract

Cancer stem cells, characterized by high tumorigenicity and drug-resistance, are often responsible for tumor progression and metastasis. Aldehyde dehydrogenases, often overexpressed in cancer stem cells enriched tumors, present a potential target for specific anti-cancer stem cells treatment. In this study, we report a self-assembled nano-prodrug composed of aldehyde dehydrogenases activatable photosensitizer and disulfide-linked all-trans retinoic acid for diagnosis and targeted treatment of cancer stem cells enriched tumors. The disulfide-linked all-trans retinoic acid can load with photosensitizer and self-assemble into a stable nano-prodrug, which can be disassembled into all-trans retinoic acid and photosensitizer in cancer stem cells by high level of glutathione. As for the released photosensitizer, overexpressed aldehyde dehydrogenase catalyzes the oxidation of aldehydes to carboxyl under cancer stem cells enriched microenvironment, activating the generation of reactive oxygen species and fluorescence emission. This generation of reactive oxygen species leads to direct killing of cancer stem cells and is accompanied by a noticeable fluorescence enhancement for real-time monitoring of the cancer stem cells enriched microenvironment. Moreover, the released all-trans retinoic acid, as a differentiation agent, reduce the cancer stem cells stemness and improve the cancer stem cells enriched microenvironment, offering a synergistic effect for enhanced anti-cancer stem cells treatment of photosensitizer in inhibition of in vivo tumor growth and metastasis.

摘要

肿瘤干细胞具有高致瘤性和耐药性,常导致肿瘤的进展和转移。醛脱氢酶在富含肿瘤干细胞的肿瘤中常过度表达,是一种潜在的特异性抗癌干细胞治疗靶点。在本研究中,我们报告了一种由醛脱氢酶激活型光敏剂和二硫键连接的全反式维甲酸组成的自组装纳米前药,用于诊断和靶向治疗富含肿瘤干细胞的肿瘤。二硫键连接的全反式维甲酸可以负载光敏剂并自组装成稳定的纳米前药,在富含肿瘤干细胞的高浓度谷胱甘肽环境下,二硫键连接的全反式维甲酸可以分解为全反式维甲酸和光敏剂。对于释放的光敏剂,过表达的醛脱氢酶在富含肿瘤干细胞的微环境下将醛催化氧化为羧基,激活活性氧的生成和荧光发射。这种活性氧的生成导致肿瘤干细胞的直接杀伤,并伴有明显的荧光增强,用于实时监测富含肿瘤干细胞的微环境。此外,释放的全反式维甲酸作为分化剂,降低了肿瘤干细胞的干性,并改善了富含肿瘤干细胞的微环境,为增强光敏剂抑制体内肿瘤生长和转移的抗癌干细胞治疗提供了协同作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ad/11528051/b2e6a53ae058/41467_2024_53771_Fig1_HTML.jpg

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