中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Dual-Targeting to Cancer Cells and M2 Macrophages via Biomimetic Delivery of Mannosylated Albumin Nanoparticles for Drug-Resistant Cancer Therapy

文献类型:期刊论文

作者Zhao, Pengfei2,3; Yin, Weimin2,3; Wu, Aihua3,4; Tang, Yisi3,4; Wang, Jinyu3; Pan, Zhenzhen1,3; Lin, Tingting3,5; Zhang, Meng3; Chen, Binfan3; Duan, Yifei2
刊名ADVANCED FUNCTIONAL MATERIALS
出版日期2017-11-24
卷号27期号:44
关键词albumin nanoparticles combination therapy mannose receptors multidrug resistance SPARC
ISSN号1616-301X
DOI10.1002/adfm.201700403
文献子类Article
英文摘要Multidrug resistance (MDR) is an issue that is not only related to cancer cells but also associated with the tumor microenvironments. MDR involves the complicated cancer cellular events and the crosstalk between cancer cells and their surroundings. Ideally, an effective system against MDR cancer should take dual action on both cancer cells and tumor microenvironments. The authors find that both the drug-resistant colon cancer cells and the protumor M2 macrophages highly express two nutrient transporters, i.e., secreted protein acidic and rich in cysteine (SPARC) and mannose receptors (MR). By targeting SPARC and MR, a system can act on both cancer cells and M2 macrophages. Herein the authors develop a mannosylated albumin nanoparticles with coencapsulation of different drugs, i.e., disulfiram/copper complex (DSF/Cu) and regorafenib (Rego). The results show that combination therapy of DSF/Cu and Rego efficiently inhibits the growth of drug-resistant colon tumor, and the combination has not been reported yet for use in anticancer treatment. The system significantly improves the treatment outcomes in the animal model bearing drug-resistant tumors. The therapeutic mechanisms involve enhanced apoptosis, upregulation of intracellular ROS, anti-angiogenesis, and tumor-associated macrophage "re-education." This strategy is characterized by dual targeting to and the simultaneous action on cancer cells and M2 macrophages, with biomimetic codelivery of a novel drug combination.
WOS关键词TUMOR-ASSOCIATED MACROPHAGES ; COLORECTAL-CANCER ; SPARC EXPRESSION ; PANCREATIC-CANCER ; BOUND PACLITAXEL ; NAB-PACLITAXEL ; BREAST-CANCER ; LUNG-CANCER ; AUTOPHAGY ; DISULFIRAM
资助项目National Basic Research Program of China (973 Program)[2014CB931900] ; National Basic Research Program of China (973 Program)[2013CB932503] ; NSFC, China[81373357] ; NSFC, China[81422048] ; NSFC, China[81673382] ; NSFC, China[81521005]
WOS研究方向Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics
语种英语
WOS记录号WOS:000416035400019
出版者WILEY-V C H VERLAG GMBH
源URL[http://119.78.100.183/handle/2S10ELR8/272396]  
专题药物制剂研究中心
通讯作者Huang, Yongzhuo
作者单位1.Guangxi Univ Chinese Med, Fac Pharm, 13 Wuhe Rd, Nanning 530200, Peoples R China;
2.Nanchang Univ, Coll Pharm, 461 Bayi Rd, Nanchang 330006, Jiangxi, Peoples R China;
3.Chinese Acad Sci, Shanghai Inst Mat Med, 501 Haike Rd, Shanghai 201203, Peoples R China;
4.Guangzhou Univ Chinese Med, Trop Med Inst, 12 Jichang Rd, Guangzhou 501450, Guangdong, Peoples R China;
5.Binzhou Med Univ Hosp, Dept Pharm, 661 Huanghe Rd, Binzhou 256603, Peoples R China
推荐引用方式
GB/T 7714
Zhao, Pengfei,Yin, Weimin,Wu, Aihua,et al. Dual-Targeting to Cancer Cells and M2 Macrophages via Biomimetic Delivery of Mannosylated Albumin Nanoparticles for Drug-Resistant Cancer Therapy[J]. ADVANCED FUNCTIONAL MATERIALS,2017,27(44).
APA Zhao, Pengfei.,Yin, Weimin.,Wu, Aihua.,Tang, Yisi.,Wang, Jinyu.,...&Huang, Yongzhuo.(2017).Dual-Targeting to Cancer Cells and M2 Macrophages via Biomimetic Delivery of Mannosylated Albumin Nanoparticles for Drug-Resistant Cancer Therapy.ADVANCED FUNCTIONAL MATERIALS,27(44).
MLA Zhao, Pengfei,et al."Dual-Targeting to Cancer Cells and M2 Macrophages via Biomimetic Delivery of Mannosylated Albumin Nanoparticles for Drug-Resistant Cancer Therapy".ADVANCED FUNCTIONAL MATERIALS 27.44(2017).

入库方式: OAI收割

来源:上海药物研究所

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