Intracellular trafficking of new anticancer therapeutics: antibody-drug conjugates

被引:103
|
作者
Kalim, Muhammad [1 ]
Chen, Jie [1 ]
Wang, Shenghao [1 ]
Lin, Caiyao [1 ]
Ullah, Saif [1 ]
Liang, Keying [1 ]
Ding, Qian [1 ]
Chen, Shuqing [2 ]
Zhan, Jinbiao [1 ]
机构
[1] Zhejiang Univ, Sch Med, Dept Biochem & Genet, 866 Yuhangtang Rd, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Coll Pharmaceut Sci, Dept Pharmaceut Anal, Hangzhou, Zhejiang, Peoples R China
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2017年 / 11卷
关键词
antibody-drug conjugate; antibody; endocytosis; intracellular trafficking; clathrin; GLEMBATUMUMAB VEDOTIN CDX-011; POTENT ANTITUMOR-ACTIVITY; MONOMETHYL AURISTATIN E; IN-VIVO; GEMTUZUMAB OZOGAMICIN; TRASTUZUMAB EMTANSINE; BRENTUXIMAB VEDOTIN; LORVOTUZUMAB MERTANSINE; INOTUZUMAB OZOGAMICIN; BREAST-CANCER;
D O I
10.2147/DDDT.S135571
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Antibody-drug conjugate (ADC) is a milestone in targeted cancer therapy that comprises of monoclonal antibodies chemically linked to cytotoxic drugs. Internalization of ADC takes place via clathrin-mediated endocytosis, caveolae-mediated endocytosis, and pinocytosis. Conjugation strategies, endocytosis and intracellular trafficking optimization, linkers, and drugs chemistry present a great challenge for researchers to eradicate tumor cells successfully. This inventiveness of endocytosis and intracellular trafficking has given considerable momentum recently to develop specific antibodies and ADCs to treat cancer cells. It is significantly advantageous to emphasize the endocytosis and intracellular trafficking pathways efficiently and to design potent engineered conjugates and biological entities to boost efficient therapies enormously for cancer treatment. Current studies illustrate endocytosis and intracellular trafficking of ADC, protein, and linker strategies in unloading and also concisely evaluate practically applicable ADCs.
引用
收藏
页码:2265 / 2276
页数:12
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