TY - JOUR
T1 - Tubulin inhibitor-based antibody-drug conjugates for cancer therapy
AU - Chen, Hao
AU - Lin, Zongtao
AU - Arnst, Kinsie E.
AU - Miller, Duane D.
AU - Li, Wei
N1 - Funding Information:
Acknowledgments: This work is partially supported by NIH/NCI grants R01CA148706 to WL and DDM. Zongtao Lin would like to thank the Alma and Hal Reagan Fellowship from the University of Tennessee Health Science Center. We thank Richard Redfearn at UTHSC for editorial assistance. The contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH/NCI.
Publisher Copyright:
© 2017 by the authors.
PY - 2017/8
Y1 - 2017/8
N2 - Antibody-drug conjugates (ADCs) are a class of highly potent biopharmaceutical drugs generated by conjugating cytotoxic drugs with specific monoclonal antibodies through appropriate linkers. Specific antibodies used to guide potent warheads to tumor tissues can effectively reduce undesired side effects of the cytotoxic drugs. An in-depth understanding of antibodies, linkers, conjugation strategies, cytotoxic drugs, and their molecular targets has led to the successful development of several approved ADCs. These ADCs are powerful therapeutics for cancer treatment, enabling wider therapeutic windows, improved pharmacokinetic/pharmacodynamic properties, and enhanced efficacy. Since tubulin inhibitors are one of the most successful cytotoxic drugs in the ADC armamentarium, this review focuses on the progress in tubulin inhibitor-based ADCs, as well as lessons learned from the unsuccessful ADCs containing tubulin inhibitors. This review should be helpful to facilitate future development of new generations of tubulin inhibitor-based ADCs for cancer therapy.
AB - Antibody-drug conjugates (ADCs) are a class of highly potent biopharmaceutical drugs generated by conjugating cytotoxic drugs with specific monoclonal antibodies through appropriate linkers. Specific antibodies used to guide potent warheads to tumor tissues can effectively reduce undesired side effects of the cytotoxic drugs. An in-depth understanding of antibodies, linkers, conjugation strategies, cytotoxic drugs, and their molecular targets has led to the successful development of several approved ADCs. These ADCs are powerful therapeutics for cancer treatment, enabling wider therapeutic windows, improved pharmacokinetic/pharmacodynamic properties, and enhanced efficacy. Since tubulin inhibitors are one of the most successful cytotoxic drugs in the ADC armamentarium, this review focuses on the progress in tubulin inhibitor-based ADCs, as well as lessons learned from the unsuccessful ADCs containing tubulin inhibitors. This review should be helpful to facilitate future development of new generations of tubulin inhibitor-based ADCs for cancer therapy.
KW - Antibody-drug conjugates
KW - Cytotoxic payloads
KW - Linker
KW - Monoclonal antibody
KW - Site-specific conjugation
KW - Tubulin inhibitors
UR - http://www.scopus.com/inward/record.url?scp=85027968777&partnerID=8YFLogxK
U2 - 10.3390/molecules22081281
DO - 10.3390/molecules22081281
M3 - Review article
C2 - 28763044
AN - SCOPUS:85027968777
SN - 1420-3049
VL - 22
JO - Molecules
JF - Molecules
IS - 8
M1 - 1281
ER -