Malemud Charles J, Blumenthal David E
Charles J Malemud, David E Blumenthal, The Arthritis Research Laboratory, Department of Medicine, Division of Rheumatic Diseases, Case Western Reserve University, Cleveland, OH 44106-5076, United States.
World J Orthop. 2014 Sep 18;5(4):496-503. doi: 10.5312/wjo.v5.i4.496.
Medicinal chemistry strategies have contributed to the development, experimental study of and clinical trials assessment of the first type of protein kinase small molecule inhibitor to target the Janus kinase/Signal Transducers and Activators of Transcription (JAK/STAT) signaling pathway. The orally administered small molecule inhibitor, tofacitinib, is the first drug to target the JAK/STAT pathway for entry into the armamentarium of the medical therapy of rheumatoid arthritis. The introduction of tofacitinib into general rheumatologic practice coupled with increasing understanding that additional cellular signal transduction pathways including the mitogen-activated protein kinase and phosphatidylinositide-3-kinase/Akt/mammalian target of rapamycin pathways as well as spleen tyrosine kinase also contribute to immune-mediated inflammatory in rheumatoid arthritis makes it likely that further development of orally administered protein kinase small molecule inhibitors for rheumatoid arthritis will occur in the near future.
药物化学策略推动了针对Janus激酶/信号转导及转录激活因子(JAK/STAT)信号通路的第一类蛋白激酶小分子抑制剂的研发、实验研究及临床试验评估。口服小分子抑制剂托法替布是首个靶向JAK/STAT通路并进入类风湿关节炎药物治疗手段的药物。托法替布引入一般风湿病治疗实践,同时人们越来越认识到包括丝裂原活化蛋白激酶和磷脂酰肌醇-3-激酶/蛋白激酶B/雷帕霉素哺乳动物靶标通路以及脾酪氨酸激酶在内的其他细胞信号转导通路也在类风湿关节炎的免疫介导炎症中发挥作用,这使得口服蛋白激酶小分子抑制剂在类风湿关节炎治疗方面的进一步研发在不久的将来很可能会出现。