Yi Taolin, Lindner Daniel
Department of Cancer Biology, Lerner Research Institute, Cleveland Clinic, NB40, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Curr Oncol Rep. 2008 Mar;10(2):114-21. doi: 10.1007/s11912-008-0019-6.
Protein tyrosine phosphatases (PTPases) are attractive targets for developing novel cancer therapeutics. Activated via gain-of-function point mutations or overexpression, several PTPases have been identified as critical oncogenic molecules in human malignancies that may be targeted with small chemical inhibitors as a therapeutic strategy. Tumor suppressor PTPases have also been discovered as contributing factors in cancer development that may be targeted via intervention of downstream signaling events for therapeutic purposes. In addition, PTPases have been identified as key negative regulators of cytokines or immune cells. Targeting these negative PTPases may improve the efficacy of cytokine therapy and immunotherapy, which currently have modest response rates and limited survival benefit. Inhibitors of selective PTPases have demonstrated significant preclinical antitumor activity, leading to early-phase clinical trials. Further research and development could lead to PTPase-targeted cancer therapeutics in the near future.
蛋白质酪氨酸磷酸酶(PTPases)是开发新型癌症治疗药物的有吸引力的靶点。通过功能获得性点突变或过表达激活后,几种PTPases已被确定为人类恶性肿瘤中的关键致癌分子,可作为治疗策略用小分子化学抑制剂进行靶向治疗。肿瘤抑制性PTPases也被发现是癌症发展的促成因素,可通过干预下游信号事件进行靶向治疗。此外,PTPases已被确定为细胞因子或免疫细胞的关键负调节因子。靶向这些负性PTPases可能会提高细胞因子疗法和免疫疗法的疗效,目前这两种疗法的缓解率适中且生存获益有限。选择性PTPases抑制剂已显示出显著的临床前抗肿瘤活性,从而进入了早期临床试验。进一步的研发可能在不久的将来带来以PTPases为靶点的癌症治疗药物。