Fabbro Doriano
PIQUR Therapeutics AG, Basel, Switzerland
Mol Pharmacol. 2015 May;87(5):766-75. doi: 10.1124/mol.114.095489. Epub 2014 Dec 30.
Deregulation of protein and lipid kinase activities leads to a variety of pathologies, ranging from cancer inflammatory diseases, diabetes, infectious diseases, and cardiovascular disorders. Protein kinases and lipid kinases represent, therefore, an important target for the pharmaceutical industry. In fact, approximately one-third of all protein targets under investigation in the pharmaceutical industry are protein or lipid kinases. To date, 30 kinase inhibitors have been approved, which, with few exceptions, are mainly for oncological indications and directed against only a handful of protein and lipid kinases, leaving 70% of the kinome untapped. Despite these successes in kinase drug discovery, the development of kinase inhibitors with outstanding selectivity, identification and validation of driver kinase(s) in diseases, and the emerging problem of resistance to the inhibition of key target kinases remain major challenges. This minireview provides an insight into protein and lipid kinase drug discovery with respect to achievements, binding modes of inhibitors, and novel avenues for the generation of second-generation kinase inhibitors to treat cancers.
蛋白质和脂质激酶活性的失调会导致多种病理状况,范围涵盖癌症、炎症性疾病、糖尿病、传染病和心血管疾病。因此,蛋白质激酶和脂质激酶是制药行业的重要靶点。事实上,制药行业正在研究的所有蛋白质靶点中,约三分之一是蛋白质或脂质激酶。迄今为止,已有30种激酶抑制剂获批,除少数例外,这些抑制剂主要用于肿瘤适应症,且仅针对少数几种蛋白质和脂质激酶,激酶组中70%尚未开发。尽管在激酶药物研发方面取得了这些成功,但开发具有卓越选择性的激酶抑制剂、识别和验证疾病中的驱动激酶,以及对关键靶点激酶抑制产生耐药性这一新兴问题,仍然是重大挑战。本综述简要介绍了蛋白质和脂质激酶药物研发在成果、抑制剂结合模式以及开发用于治疗癌症的第二代激酶抑制剂新途径等方面的情况。