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具有pH响应性的去甲斑蝥素/铜双消耗谷胱甘肽纳米催化剂用于CT/CDT协同癌症治疗

Norcantharidin/Cu dual-depleting GSH nanocatalyst with pH-responsive for CT/CDT synergistic cancer therapy.

作者信息

Guo Xiaohuan, Cai Bingbing, Fang Qi, Chen Yanyan, Zhou Yuzhu, Liang Zhixing, Wen Changchun, Liu Yan-Cheng, Liang Hong

机构信息

State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, 541004, China.

出版信息

Mater Today Bio. 2025 Jun 6;33:101959. doi: 10.1016/j.mtbio.2025.101959. eCollection 2025 Aug.

Abstract

The high level of glutathione (GSH) in tumor cells can consume reactive oxygen species (ROS), seriously affecting the efficacy of chemodynamic therapy (CDT). Although it took a great deal of effort, developing a tumor-specific CDT that efficiently depletes GSH remains a formidable challenge. Herein, we propose a pH-responsive nanocatalyst containing the active molecule norcantharidin (NCTD) and Cu for dual GSH depletion, achieving efficient GSH depletion. Due to the weakly acidic tumor microenvironment (TME), the catalyst releases NCTD and Cu in a pH-responsive manner for the synergistic therapy of chemotherapy (CT) and CDT. Both components consume GSH and subsequently produce ROS, reducing the antioxidant capacity of cancer cells while increasing oxidative stress. This disrupts cellular redox homeostasis, leading to mitochondrial dysfunction and inducing tumor cell apoptosis. This work not only develops nanomaterials with dual GSH depletion capabilities for high-efficiency CDT but also achieves synergistic CT and CDT tumor therapy with the addition of NCTD, an active ingredient of traditional Chinese medicine.

摘要

肿瘤细胞中高水平的谷胱甘肽(GSH)能够消耗活性氧(ROS),严重影响化学动力疗法(CDT)的疗效。尽管付出了巨大努力,但开发一种能有效消耗GSH的肿瘤特异性CDT仍然是一项艰巨的挑战。在此,我们提出了一种含有活性分子去甲斑蝥素(NCTD)和铜的pH响应型纳米催化剂,用于双重消耗GSH,实现高效的GSH消耗。由于肿瘤微环境(TME)呈弱酸性,该催化剂以pH响应的方式释放NCTD和铜,用于化疗(CT)和CDT的协同治疗。两种成分都消耗GSH,随后产生活性氧,降低癌细胞的抗氧化能力,同时增加氧化应激。这会破坏细胞氧化还原稳态,导致线粒体功能障碍并诱导肿瘤细胞凋亡。这项工作不仅开发了具有双重GSH消耗能力的纳米材料用于高效CDT,还通过添加中药活性成分NCTD实现了CT和CDT的协同肿瘤治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85aa/12180979/f153bdf1760d/ga1.jpg

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