Ventura Juan-José, Nebreda Angel R
Spanish National Cancer Center (CNIO), Madrid, Spain.
Clin Transl Oncol. 2006 Mar;8(3):153-60. doi: 10.1007/s12094-006-0005-0.
Protein phosphorylation plays key roles in many physiological processes and is often deregulated in pathological conditions. Our current understanding of how protein kinases and phosphatases orchestrate the phosphorylation changes that control cellular functions has made these enzymes potential drug targets for the treatment of many diseases. The success of the tyrosine kinase inhibitor Gleevec in the treatment of some cancers has further invigorated the development of kinase inhibitors as anti-cancer drugs. A large number of these compounds are currently undergoing clinical trials and there is much expectation on the therapeutic potential of these molecules, as more specific and less toxic drugs than currently used generic chemotherapeutic agents. In this manuscript, we review the current status of more than 30 protein kinase inhibitors with proven or potential therapeutic value for cancer treatment. These include inhibitors of receptor and cytosolic tyrosine kinases as well as compounds that target different families of serine/threonine kinases involved in signalling and cell cycle regulation. We also briefly touch on the prospects of phosphatase inhibitors. The combination of kinase inhibitors to target different components of signalling pathways that are found deregulated in tumours is also emerging as an interesting approach for cancer therapy.
蛋白质磷酸化在许多生理过程中发挥着关键作用,且在病理状态下常常失调。我们目前对蛋白激酶和磷酸酶如何协调控制细胞功能的磷酸化变化的理解,使得这些酶成为治疗多种疾病的潜在药物靶点。酪氨酸激酶抑制剂格列卫在治疗某些癌症方面的成功,进一步推动了激酶抑制剂作为抗癌药物的研发。目前大量此类化合物正在进行临床试验,人们对这些分子的治疗潜力寄予厚望,因为它们比目前使用的通用化疗药物更具特异性且毒性更小。在本手稿中,我们综述了30多种对癌症治疗具有已证实或潜在治疗价值的蛋白激酶抑制剂的现状。这些抑制剂包括受体和胞质酪氨酸激酶的抑制剂,以及靶向参与信号传导和细胞周期调控的不同丝氨酸/苏氨酸激酶家族的化合物。我们还简要提及了磷酸酶抑制剂的前景。联合使用激酶抑制剂来靶向肿瘤中发现失调的信号通路的不同组分,也正成为一种有趣的癌症治疗方法。