Johnson Theodore O, Ermolieff Jacques, Jirousek Michael R
Pfizer Global Research and Development, La Jolla Laboratories, 10770 Science Center Drive, San Diego, California 92121, USA.
Nat Rev Drug Discov. 2002 Sep;1(9):696-709. doi: 10.1038/nrd895.
Increased incidence of type 2 diabetes mellitus and obesity has elevated the medical need for new agents to treat these disease states. Resistance to the hormones insulin and leptin are hallmarks of both type 2 diabetes and obesity. Drugs that can ameliorate this resistance should be effective in treating type 2 diabetes and possibly obesity. Protein tyrosine phosphatase 1B (PTP1B) is thought to function as a negative regulator of insulin and leptin signal transduction. This article reviews PTP1B as a novel target for type 2 diabetes, and looks at the challenges in developing small-molecule inhibitors of this phosphatase.
2型糖尿病和肥胖症发病率的上升增加了对治疗这些疾病状态的新型药物的医疗需求。对激素胰岛素和瘦素的抵抗是2型糖尿病和肥胖症的标志。能够改善这种抵抗的药物应该对治疗2型糖尿病以及可能对治疗肥胖症有效。蛋白酪氨酸磷酸酶1B(PTP1B)被认为是胰岛素和瘦素信号转导的负调节因子。本文综述了PTP1B作为2型糖尿病的新型靶点,并探讨了开发这种磷酸酶的小分子抑制剂所面临的挑战。