Grant S K
Department of Biochemical Pharmacology, Pfizer Global Research & Development, Pfizer La Jolla Laboratories, 10777 Science Center Drive, San Diego, CA 92121, USA.
Cell Mol Life Sci. 2009 Apr;66(7):1163-77. doi: 10.1007/s00018-008-8539-7.
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.
蛋白激酶抑制剂是一类重要且仍在不断涌现的靶向治疗药物。药物研发策略探索了多种方法来靶向抑制蛋白激酶信号传导。本综述将重点介绍一些促成治疗性蛋白激酶抑制剂成功临床开发的策略,尤其是作为抗癌药物的情况。在开发针对生长因子或受体酪氨酸激酶的新型蛋白质和基于寡核苷酸的生物制剂方面已取得了一些显著进展。此外,在合理设计靶向独特激酶构象形式和结合位点且具有特定激酶选择性谱的小分子抑制剂方面也取得了进展。还将综述与这些激酶靶向药物相关的一些潜在临床毒性和不良副作用。治疗性蛋白激酶抑制剂已使癌症患者受益匪浅,并有望为其他疾病带来未来的治疗方法。