Microtubule inhibitor-based antibody-drug conjugates for cancer therapy

被引:50
|
作者
Klute, Kelsey [1 ]
Nackos, Eleni [1 ]
Tasaki, Shinsuke [1 ]
Nguyen, Daniel P. [2 ]
Bander, Neil H. [2 ]
Tagawa, Scott T. [1 ,2 ]
机构
[1] Weill Cornell Med Coll, Dept Med, Div Hematol & Med Oncol, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Dept Urol, New York, NY 10065 USA
来源
ONCOTARGETS AND THERAPY | 2014年 / 7卷
关键词
monoclonal antibody; antibody-drug conjugate; microtubule inhibitor; METASTATIC BREAST-CANCER; LARGE-CELL LYMPHOMA; PHASE-I TRIAL; RESISTANT PROSTATE-CANCER; ACUTE MYELOID-LEUKEMIA; BRENTUXIMAB VEDOTIN SGN-35; NON-HODGKINS-LYMPHOMA; MEMBRANE ANTIGEN; MONOCLONAL-ANTIBODY; GEMTUZUMAB OZOGAMICIN;
D O I
10.2147/OTT.S46887
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The specificity of monoclonal antibodies represents a potential therapeutic advantage, but their use as single agents in oncology has proven limited to date. The development of antibody-drug conjugates (ADCs) takes advantage of the specificity of the monoclonal antibody and potent cytotoxic effect of chemotherapy, leading to enhanced cytotoxicity in target cells and limiting toxicity to normal tissue. Microtubules represent a validated oncologic target in a range of tumor types, with a number of anti-microtubule targeting cytotoxic drugs approved for cancer use. The systemic use of potent microtubule-binding agents is limited by their effects in normal cells, which leads to toxicity including myelosuppression and peripheral neuropathy. Linking these agents to monoclonal antibodies may limit toxicity to normal tissues and increase drug concentration in target tissues, also allowing the use of more potent agents which would be too toxic to administer in their unbound form. Two such ADCs have been approved for clinical use and many others are in development. Here we review the characteristics of each of the ADC components that have led to efficacious therapies and discuss some of the tubulin inhibitor-based ADCs in development for cancer therapy.
引用
收藏
页码:2227 / 2236
页数:10
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