Antiglioma via regulating oxidative stress and remodeling tumor-associated macrophage using lactoferrin-mediated biomimetic codelivery of simvastatin/fenretinide
文献类型:期刊论文
作者 | Mo, Xiaopeng2,3; Zheng, Zening1,3; He, Yang3; Zhone, Huihai2,3; Kane, Xuejia1,3; Shi, Mingjie3; Liu, Tuanbing3; Jiao, Zheng2; Huang, Yongzhuo3![]() |
刊名 | JOURNAL OF CONTROLLED RELEASE
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出版日期 | 2018-10-10 |
卷号 | 287页码:12-23 |
关键词 | Lactoferrin nanoparticle Reactive oxygen species Tumor-associated macrophages Brain-targeted delivery Biomimetic delivery Cell penetrating peptide Fenretinide Simvastatin |
ISSN号 | 0168-3659 |
DOI | 10.1016/j.jconrel.2018.08.012 |
文献子类 | Article |
英文摘要 | Effective treatment of malignant glioma still remains a formidable challenge due to lack of the effective BBB-permeable drugs and efficient brain delivery methods, and the pharmacotherapy options are very limited. Therefore, to develop an effective therapeutic strategy is a pressing need. In this work, a noncytotoxic drug combination (i.e., simvastatin and fenretinide) was revealed to be potent for treating glioma, which was co-encapsulated into a TPGS-TAT-embedded lactoferrin nanoparticle system for achieving brain-targeted biomimetic delivery via the LRP-1 receptor. It was shown that the lactoferrin nanoparticle repolarized the tumor-associated macrophages from the M2 phenotype to M1 via regulating the STAT6 pathway, as well as induced the ROS-mediated mitochondrial apoptosis by inhibiting the Ras/Raf/p-Erk pathway in the glioma cells. The antiglioma efficacy was further demonstrated in both the subcutaneous and orthotopic glioma models. The repolarization of tumor-associated macrophages not only prompted the ROS generation but also induced the innate immunity (e.g., anti-tumor cytokine release). This delivery and therapeutic strategy provides a novel modality for the glioma treatment. |
WOS关键词 | RANDOMIZED PHASE-III ; JNK ACTIVATION ; CANCER-CELLS ; DELIVERY ; GLIOMA ; FENRETINIDE ; APOPTOSIS ; ROS ; MICROENVIRONMENT ; EPIDEMIOLOGY |
资助项目 | 973 Program, China[2014CB931900] ; NFSC[814022883] ; NFSC[81422048] ; NFSC[81673382] ; NFSC[81521005] ; Strategic Priority Research Program of CAS[XDA12050307] ; National Special Project for Significant New Drugs Development[2018ZX09711002-010-002] ; CAS Scientific Research and Equipment Development Project[YZ201437] ; Fudan-SIMM Joint Research Fund[FU-SIMM20174009] |
WOS研究方向 | Chemistry ; Pharmacology & Pharmacy |
语种 | 英语 |
WOS记录号 | WOS:000445127000002 |
出版者 | ELSEVIER SCIENCE BV |
源URL | [http://119.78.100.183/handle/2S10ELR8/279535] ![]() |
专题 | 药物制剂研究中心 中科院受体结构与功能重点实验室 新药研究国家重点实验室 |
通讯作者 | Huang, Yongzhuo |
作者单位 | 1.Guangzhou Univ Chinese Med, Inst Trop Med, Guangzhou 510405, Guangdong, Peoples R China 2.Shanghai Univ, Coll Sci, Shanghai 200444, Peoples R China; 3.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, 501 Haike Rd, Shanghai 201203, Peoples R China; |
推荐引用方式 GB/T 7714 | Mo, Xiaopeng,Zheng, Zening,He, Yang,et al. Antiglioma via regulating oxidative stress and remodeling tumor-associated macrophage using lactoferrin-mediated biomimetic codelivery of simvastatin/fenretinide[J]. JOURNAL OF CONTROLLED RELEASE,2018,287:12-23. |
APA | Mo, Xiaopeng.,Zheng, Zening.,He, Yang.,Zhone, Huihai.,Kane, Xuejia.,...&Huang, Yongzhuo.(2018).Antiglioma via regulating oxidative stress and remodeling tumor-associated macrophage using lactoferrin-mediated biomimetic codelivery of simvastatin/fenretinide.JOURNAL OF CONTROLLED RELEASE,287,12-23. |
MLA | Mo, Xiaopeng,et al."Antiglioma via regulating oxidative stress and remodeling tumor-associated macrophage using lactoferrin-mediated biomimetic codelivery of simvastatin/fenretinide".JOURNAL OF CONTROLLED RELEASE 287(2018):12-23. |
入库方式: OAI收割
来源:上海药物研究所
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