Leeds Institute of Medical Research at St. James's, School of Medicine, University of Leeds, Leeds LS9 7TF, UK.
Cells. 2024 Jan 25;13(3):231. doi: 10.3390/cells13030231.
Advances in immunotherapy have brought significant therapeutic benefits to many cancer patients. Nonetheless, many cancer types are refractory to current immunotherapeutic approaches, meaning that further targets are required to increase the number of patients who benefit from these technologies. Protein tyrosine phosphatases (PTPs) have long been recognised to play a vital role in the regulation of cancer cell biology and the immune response. In this review, we summarize the evidence for both the pro-tumorigenic and tumour-suppressor function of non-receptor PTPs in cancer cells and discuss recent data showing that several of these enzymes act as intracellular immune checkpoints that suppress effective tumour immunity. We highlight new data showing that the deletion of inhibitory PTPs is a rational approach to improve the outcomes of adoptive T cell-based cancer immunotherapies and describe recent progress in the development of PTP inhibitors as anti-cancer drugs.
免疫疗法的进步为许多癌症患者带来了显著的治疗益处。尽管如此,许多癌症类型对当前的免疫治疗方法具有抗性,这意味着需要进一步的靶点来增加受益于这些技术的患者数量。蛋白酪氨酸磷酸酶(PTPs)长期以来一直被认为在调节癌细胞生物学和免疫反应中发挥着至关重要的作用。在这篇综述中,我们总结了非受体 PTPs 在癌细胞中促进肿瘤发生和肿瘤抑制功能的证据,并讨论了最近的数据,表明其中一些酶作为细胞内免疫检查点,抑制有效的肿瘤免疫。我们强调了新的数据,表明删除抑制性 PTPs 是改善过继 T 细胞为基础的癌症免疫疗法结果的合理方法,并描述了作为抗癌药物的 PTP 抑制剂的最新进展。