Kinase drug discovery 20 years after imatinib: progress and future directions

被引:475
作者
Cohen, Philip [1 ]
Cross, Darren [2 ]
Janne, Pasi A. [3 ]
机构
[1] Univ Dundee, Sch Life Sci, MRC Prot Phosphorylat & Ubiquitylat Unit, Dundee, Scotland
[2] AstraZeneca, Cambridge, England
[3] Harvard Univ, Lowe Ctr Thorac Oncol, Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
CELL LUNG-CANCER; CHRONIC MYELOID-LEUKEMIA; DABRAFENIB PLUS TRAMETINIB; RECEPTOR GENE-MUTATIONS; CIRCULATING TUMOR DNA; ACQUIRED-RESISTANCE; OPEN-LABEL; CLINICAL RESISTANCE; ANAPLASTIC LYMPHOMA; C-MET;
D O I
10.1038/s41573-021-00195-4
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
Protein kinases regulate nearly all aspects of cell life, and alterations in their expression, or mutations in their genes, cause cancer and other diseases. Here, we review the remarkable progress made over the past 20 years in improving the potency and specificity of small-molecule inhibitors of protein and lipid kinases, resulting in the approval of more than 70 new drugs since imatinib was approved in 2001. These compounds have had a significant impact on the way in which we now treat cancers and non-cancerous conditions. We discuss how the challenge of drug resistance to kinase inhibitors is being met and the future of kinase drug discovery. Twenty years have passed since the first small-molecule protein kinase inhibitor, imatinib, gained FDA approval. Here, Cohen et al. review advances in improving the potency and specificity of small-molecule protein kinase inhibitors and assess approaches to overcome the challenge of drug resistance. Applications of these compounds in cancers and other disorders, as well as future directions in the field, are discussed.
引用
收藏
页码:551 / 569
页数:19
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