Tumor microenvironment-activated hollow vanadium-based nanoplatform for precise therapy of lung cancer through synergistically reversing cisplatin resistance

被引：4

作者：

Ran, Lang ^{[1
]}

Xiao, Jianmin ^{[1
]}

Zhang, Weijie ^{[1
]}

Wang, Miaomiao ^{[1
]}

Xin, Huan ^{[1
]}

Li, Huimin ^{[1
]}

Hao, Hong ^{[1
]}

Wang, Maoyang ^{[1
]}

Wang, Xiaofei ^{[1
]}

Tian, Geng ^{[1
]}

Zhang, Guilong ^{[1
]}

机构：

[1] Binzhou Med Univ, Shandong Technol Innovat Ctr Mol Targeting & Intel, Sch Pharm, Yantai 264003, Peoples R China

来源：

CHEMICAL ENGINEERING JOURNAL | 2024年 / 484卷

基金：

中国国家自然科学基金;

关键词：

Cisplatin resistance; Vanadium -based Nanoplatform; Glutamyl cysteine ligase; Excision repair cross -complementing 1; Lung cancer; IN-VITRO; PRODRUG; NANOPARTICLES; CHEMOTHERAPY; MECHANISMS; DELIVERY;

D O I：

10.1016/j.cej.2024.149448

中图分类号：

X [环境科学、安全科学];

学科分类号：

08 ; 0830 ;

摘要：

The resistance and side effect of cisplatin (CDDP) were still great challenges for highly efficient therapy of lung cancer in clinic. The studies indicated that the CDDP resistance mainly involved GSH-mediated inactivation and the damaged DNA repair. Herein, a novel vanadium-based nanoplatform was designed via platelet-derived growth factor receptor-beta (PDGFR-beta)-recognizing cyclic peptide (PDGFB)-labeled liposomes coating onto the hollow vanadium-doped mesoporous silica nanoparticle (HVMSN) loaded Pt (IV) prodrugs (pLi-HVMSN-Pt). This nanoplatform actively targeted tumor tissue, and then effectively responded to weakly acidic and high GSH of tumor microenvironment, making Pt (IV) prodrugs and vanadium ions be precisely delivered and intelligently released. Moreover, the vanadium ions significantly downregulated the expression of glutamyl cysteine ligase (GCL) and excision repair cross-complementing 1 (ERCC1), which inhibited the synthesis of GSH in cells and the damaged DNA repair. These synergistic actions dramatically increased the sensitivity of tumor cells to Pt-based drug, and then reversed CDDP resistance. Furthermore, in vivo experiment results demonstrated highly efficient suppression of tumor growth induced by the pLi-HVMSN-Pt. Therefore, this work provided a novel strategy for reversing CDDP-resistance and the precise therapy of lung cancer.

引用

页数：11

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