Therapeutic Protein Kinase Inhibitors

被引:168
作者
Grant, S. K. [1 ]
机构
[1] Pfizer La Jolla Labs, Dept Biochem Pharmacol, Pfizer Global Res & Dev, San Diego, CA 92121 USA
关键词
Protein kinase; kinase inhibitor; kinase signaling; drug discovery; GROWTH-FACTOR RECEPTOR; SMALL-CELL LUNG; PP60(C-SRC) TYROSINE KINASE; ATP COMPETITIVE INHIBITORS; CYCLIN-DEPENDENT KINASES; ORAL MEK INHIBITOR; MONOCLONAL-ANTIBODY; PHASE-II; BREAST-CANCER; ANTITUMOR-ACTIVITY;
D O I
10.1007/s00018-008-8539-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Protein kinase inhibitors represent an important and still emerging class of targeted therapeutic agents. Drug discovery and development strategies have explored numerous approaches to target the inhibition of protein kinase signaling. This review will highlight some of the strategies that have led to the successful clinical development of therapeutic protein kinase inhibitors, particularly as anticancer drugs. Some notable advances have been made in the development of novel protein and oligonucleotide-based biologics that target growth factor or receptor tyrosine kinases. Also, advances have been made in the rational design of small-molecule inhibitors that target unique kinase conformational forms and binding sites, and have specific kinase selectivity profiles. A review will also be given of some of the potential clinical toxicities and adverse side-effects associated with these kinase-targeted drugs. Therapeutic protein kinase inhibitors have been highly beneficial to cancer patients and offer the promise of future therapies for other diseases as well.
引用
收藏
页码:1163 / 1177
页数:15
相关论文
共 153 条
[1]
Abrams TJ, 2003, MOL CANCER THER, V2, P1011
[2]
Monoclonal antibody therapy of cancer [J].
Adams, GP ;
Weiner, LM .
NATURE BIOTECHNOLOGY, 2005, 23 (09) :1147-1157
[3]
Phase I pharmacokinetic and pharmacodynamic study of the oral, small-molecule mitogen-activated protein kinase kinase 1/2 inhibitor AZD6244 (ARRY-142886) in patients with advanced cancers [J].
Adjei, Alex A. ;
Cohen, Roger B. ;
Franklin, Wilbur ;
Morris, Clive ;
Wilson, David ;
Molina, Julian R. ;
Hanson, Lorelei J. ;
Gore, Lia ;
Chow, Laura ;
Leong, Stephen ;
Maloney, Lara ;
Gordon, Gilad ;
Simmons, Heidi ;
Marlow, Allison ;
Litwiler, Kevin ;
Brown, Suzy ;
Poch, Gregory ;
Kane, Katie ;
Haney, Jerry ;
Eckhardt, S. Gail .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (13) :2139-2146
[4]
Enhancement of the antitumor activity of ionising radiation by nimotuzumab, a humanised monoclonal antibody to the epidermal growth factor receptor, in non-small cell lung cancer cell lines of differing epidermal growth factor receptor status [J].
Akashi, Y. ;
Okamoto, I. ;
Iwasa, T. ;
Yoshida, T. ;
Suzuki, M. ;
Hatashita, E. ;
Yamada, Y. ;
Satoh, T. ;
Fukuoka, M. ;
Ono, K. ;
Nakagawa, K. .
BRITISH JOURNAL OF CANCER, 2008, 98 (04) :749-755
[5]
Phase II study of flavopiridol in patients with advanced colorectal cancer [J].
Aklilu, M ;
Kindler, HL ;
Donehower, RC ;
Mani, S ;
Vokes, EE .
ANNALS OF ONCOLOGY, 2003, 14 (08) :1270-1273
[6]
Targeting the unactivated conformations of protein kinases for small molecule drug discovery [J].
Alton, Gordon R. ;
Lunney, Elizabeth A. .
EXPERT OPINION ON DRUG DISCOVERY, 2008, 3 (06) :595-605
[7]
Congestive heart failure is a rare event in patients receiving imatinib therapy [J].
Atallah, Ehab ;
Durand, Jean-Bernard ;
Kantarjian, Hagop ;
Cortes, Jorge .
BLOOD, 2007, 110 (04) :1233-1237
[8]
Intravitreal bevacizumab (Avastin) for neovascular age-related macular degeneration [J].
Avery, RL ;
Pieramici, DJ ;
Rabena, MD ;
Castellarin, AA ;
Nasir, MA ;
Giust, MJ .
OPHTHALMOLOGY, 2006, 113 (03) :363-372
[9]
The selectivity of protein kinase inhibitors: a further update [J].
Bain, Jenny ;
Plater, Lorna ;
Elliott, Matt ;
Shpiro, Natalia ;
Hastie, C. James ;
Mclauchlan, Hilary ;
Klevernic, Iva ;
Arthur, J. Simon C. ;
Alessi, Dario R. ;
Cohen, Philip .
BIOCHEMICAL JOURNAL, 2007, 408 :297-315
[10]
A phase I trial of the selective oral cyclin-dependent kinase inhibitor seliciclib (CYC202; R-Roscovitine), administered twice daily for 7 days every 21 days [J].
Benson, C. ;
White, J. ;
De Bono, J. ;
O'Donnell, A. ;
Raynaud, F. ;
Cruickshank, C. ;
McGrath, H. ;
Walton, M. ;
Workman, P. ;
Kaye, S. ;
Cassidy, J. ;
Gianella-Borradori, A. ;
Judson, I. ;
Twelves, C. .
BRITISH JOURNAL OF CANCER, 2007, 96 (01) :29-37