Field Guide to Challenges and Opportunities in Antibody Drug Conjugates for Chemists

被引:79
作者
Gordon, Mallory R. [1 ]
Canakci, Mine [2 ]
Li, Longyu [1 ]
Zhuang, Jiaming [1 ]
Osborne, Barbara [2 ,3 ]
Thayumanavan, S. [1 ,2 ]
机构
[1] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
[2] Univ Massachusetts, Mol & Cellular Biol Program, Amherst, MA 01003 USA
[3] Univ Massachusetts, Dept Vet & Anim Sci, Amherst, MA 01003 USA
基金
美国国家卫生研究院;
关键词
ACUTE MYELOID-LEUKEMIA; SITE-SPECIFIC CONJUGATION; METASTATIC BREAST-CANCER; PICTET-SPENGLER LIGATION; MONOCLONAL-ANTIBODY; IN-VIVO; GEMTUZUMAB OZOGAMICIN; CALICHEAMICIN CONJUGATE; TRASTUZUMAB EMTANSINE; PROTEIN CONJUGATION;
D O I
10.1021/acs.bioconjchem.5b00399
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Antibody-drug conjugates have attracted a great amount of attention as a therapeutic strategy for diseases where targeting specific tissues and cells are critical components, such as in cancer therapy. Although promising, the number of approved ADC drugs is relatively limited. This emanates from the challenges associated with generating the conjugates and the complexities associated with the stability requirements for these conjugates during circulation and after reaching the target. Here, we provide a comprehensive overview of the design challenges facing the ADC field. These challenges also provide several unique research and development opportunities, which are also highlighted throughout the review.
引用
收藏
页码:2198 / 2215
页数:18
相关论文
共 118 条
[81]   Targeting HER2-Positive Breast Cancer with Trastuzumab-DM1, an Antibody-Cytotoxic Drug Conjugate [J].
Phillips, Gail D. Lewis ;
Li, Guangmin ;
Dugger, Debra L. ;
Crocker, Lisa M. ;
Parsons, Kathryn L. ;
Mai, Elaine ;
Blattler, Walter A. ;
Lambert, John M. ;
Chari, Ravi V. J. ;
Lutz, Robert J. ;
Wong, Wai Lee T. ;
Jacobson, Frederic S. ;
Koeppen, Hartmut ;
Schwall, Ralph H. ;
Kenkare-Mitra, Sara R. ;
Spencer, Susan D. ;
Sliwkowski, Mark X. .
CANCER RESEARCH, 2008, 68 (22) :9280-9290
[82]   Site-specific chemical protein conjugation using genetically encoded aldehyde tags [J].
Rabuka, David ;
Rush, Jason S. ;
deHart, Gregory W. ;
Wu, Peng ;
Bertozzi, Carolyn R. .
NATURE PROTOCOLS, 2012, 7 (06) :1052-1067
[83]   SITE-SPECIFIC COVALENT MODIFICATION OF MONOCLONAL-ANTIBODIES - INVITRO AND INVIVO EVALUATIONS [J].
RODWELL, JD ;
ALVAREZ, VL ;
CHYI, L ;
LOPES, AD ;
GOERS, JWF ;
KING, HD ;
POWSNER, HJ ;
MCKEARN, TJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2632-2636
[84]   FcRn: the neonatal Fc receptor comes of age [J].
Roopenian, Derry C. ;
Akilesh, Shreeram .
NATURE REVIEWS IMMUNOLOGY, 2007, 7 (09) :715-725
[85]   Single-molecule imaging of EGFR signalling on the surface of living cells [J].
Sako, Y ;
Minoguchi, S ;
Yanagida, T .
NATURE CELL BIOLOGY, 2000, 2 (03) :168-172
[86]   N-terminal labeling of proteins by the Pictet-Spengler reaction [J].
Sasaki, Tsubasa ;
Kodama, Koichiro ;
Suzuki, Hiroaki ;
Fukuzawa, Seketsu ;
Tachibana, Kazuo .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (16) :4550-4553
[87]   A modeling analysis of the effects of molecular size and binding affinity on tumor targeting [J].
Schmidt, Michael M. ;
Wittrup, K. Dane .
MOLECULAR CANCER THERAPEUTICS, 2009, 8 (10) :2861-2871
[88]   DISPOSITION OF A MURINE MONOCLONAL-ANTIBODY VINCA CONJUGATE (KS1/4-DAVLB) IN PATIENTS WITH ADENOCARCINOMAS [J].
SCHNECK, D ;
BUTLER, F ;
DUGAN, W ;
LITTRELL, D ;
PETERSEN, B ;
BOWSHER, R ;
DELONG, A ;
DORRBECKER, S .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1990, 47 (01) :36-41
[89]   The discovery and development of brentuximab vedotin for use in relapsed Hodgkin lymphoma and systemic anaplastic large cell lymphoma [J].
Senter, Peter D. ;
Sievers, Eric L. .
NATURE BIOTECHNOLOGY, 2012, 30 (07) :631-637
[90]   Antibody Glycosylation and Inflammation [J].
Shade, Kai-Ting C. ;
Anthony, Robert M. .
ANTIBODIES, 2013, 2 (03) :392-414