Department of Health Promotion Sciences, Maternal and Infant Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
Anticancer Agents Med Chem. 2019;19(17):2036-2046. doi: 10.2174/1871520619666190906160848.
The JAK-STAT pathway is an important physiologic regulator of different cellular functions including proliferation, apoptosis, differentiation, and immunological responses. Out of six different STAT proteins, STAT5 plays its main role in hematopoiesis and constitutive STAT5 activation seems to be a key event in the pathogenesis of several hematological malignancies. This has led many researchers to develop compounds capable of inhibiting STAT5 activation or interfering with its functions. Several anti-STAT5 molecules have shown potent STAT5 inhibitory activity in vitro. However, compared to the large amount of clinical studies with JAK inhibitors that are currently widely used in the clinics to treat myeloproliferative disorders, the clinical trials with STAT5 inhibitors are very limited. At present, a few STAT5 inhibitors are in phase I or II clinical trials for the treatment of leukemias and graft vs host disease. These studies seem to indicate that such compounds could be well tolerated and useful in reducing the occurrence of resistance to tyrosine kinase inhibitors in chronic myeloid leukemia. Of interest, STAT5 seems to play an important role in the regulation of hematopoietic stem cell self-renewal suggesting that combination therapies including STAT5 inhibitors can erode the cancer stem cell pool and possibly open the way for the complete cancer eradication. In this review, we discuss the implication of STAT5 in hematological malignancies and the results obtained with the novel STAT5 inhibitors.
JAK-STAT 通路是调节多种细胞功能的重要生理调节剂,包括增殖、凋亡、分化和免疫反应。在六种不同的 STAT 蛋白中,STAT5 在造血中起着主要作用,而组成性 STAT5 激活似乎是几种血液恶性肿瘤发病机制中的关键事件。这促使许多研究人员开发能够抑制 STAT5 激活或干扰其功能的化合物。一些抗 STAT5 分子在体外显示出很强的 STAT5 抑制活性。然而,与目前临床上广泛用于治疗骨髓增生性疾病的大量 JAK 抑制剂的临床研究相比,STAT5 抑制剂的临床试验非常有限。目前,一些 STAT5 抑制剂正在进行治疗白血病和移植物抗宿主病的 I 期或 II 期临床试验。这些研究似乎表明,这些化合物可能具有良好的耐受性,并有助于减少慢性髓性白血病对酪氨酸激酶抑制剂的耐药性。有趣的是,STAT5 似乎在造血干细胞自我更新的调节中起着重要作用,这表明包括 STAT5 抑制剂在内的联合治疗可以侵蚀癌症干细胞池,并可能为彻底消除癌症开辟道路。在这篇综述中,我们讨论了 STAT5 在血液恶性肿瘤中的作用以及新型 STAT5 抑制剂的研究结果。