Ferritin drug carrier (FDC) for tumor targeting therapy

被引:171
作者
He, Jiuyang [1 ,2 ]
Fan, Kelong [1 ]
Yan, Xiyun [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Biophys, CAS Engn Lab Nanozyme, Key Lab Prot & Peptide Pharmaceut, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Savaid Med Sch, Beijing 100049, Peoples R China
[3] Zhengzhou Univ, Joint Lab Nanozymes Zhengzhou Univ, Acad Med Sci, Zhengzhou 450052, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Ferritin drug carrier (FDC); Tumor targeting; TfR1; Nanoparticles; Nanocarrier; Antibody-drug conjugates (ADC); H-FERRITIN; LOADED APOFERRITIN; BREAST-CANCER; PROTEIN-CAGE; PHOTODYNAMIC THERAPY; SELECTIVE DELIVERY; WATER-SOLUBILITY; NANOPARTICLES; DOXORUBICIN; NANOCAGES;
D O I
10.1016/j.jconrel.2019.09.002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ferritin is an iron storage protein that plays a key role in iron homeostasis and anti-oxidation of cells. Due to its unique architecture of 24 self-assembling subunits and hollow cavity capable of encapsulating drugs, and an outer surface that can be modified genetically and chemically for additional functionality, ferritin has recently emerged as a promising drug delivery vehicle. Recent research demonstrated that unmodified human heavy chain ferritin binds to its receptor, transferrin receptor 1 (TfR1), in different types of tumor tissues, including lung and breast cancer, thus highlighting the potential use of ferritin for tumor-targeting applications. In this review, we consider the many favorable characteristics of ferritin drug carriers (FDCs) for tumor drug delivery. In particular, compared with antibody-drug conjugates (ADCs), ferritin exhibits superiority in a range of attributes, including drug loading ability, thermostability, and ease of production. Thus, the emergence of FDCs may be the next step in targeted cancer therapy.
引用
收藏
页码:288 / 300
页数:13
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