Brachet-Botineau Marie, Polomski Marion, Neubauer Heidi A, Juen Ludovic, Hédou Damien, Viaud-Massuard Marie-Claude, Prié Gildas, Gouilleux Fabrice
Leukemic Niche and Oxidative metabolism (LNOx), CNRS ERL 7001, University of Tours, 37000 Tours, France.
Innovation Moléculaire et Thérapeutique (IMT), EA 7501, University of Tours, 37000 Tours, France.
Cancers (Basel). 2020 Jan 18;12(1):240. doi: 10.3390/cancers12010240.
Signal Transducer and Activator of Transcription (STAT) 3 and 5 are important effectors of cellular transformation, and aberrant STAT3 and STAT5 signaling have been demonstrated in hematopoietic cancers. STAT3 and STAT5 are common targets for different tyrosine kinase oncogenes (TKOs). In addition, STAT3 and STAT5 proteins were shown to contain activating mutations in some rare but aggressive leukemias/lymphomas. Both proteins also contribute to drug resistance in hematopoietic malignancies and are now well recognized as major targets in cancer treatment. The development of inhibitors targeting STAT3 and STAT5 has been the subject of intense investigations during the last decade. This review summarizes the current knowledge of oncogenic STAT3 and STAT5 functions in hematopoietic cancers as well as advances in preclinical and clinical development of pharmacological inhibitors.
信号转导与转录激活因子(STAT)3和5是细胞转化的重要效应因子,造血系统癌症中已证实存在STAT3和STAT5信号异常。STAT3和STAT5是不同酪氨酸激酶致癌基因(TKO)的常见靶点。此外,在一些罕见但侵袭性强的白血病/淋巴瘤中,STAT3和STAT5蛋白显示出激活突变。这两种蛋白还导致造血系统恶性肿瘤产生耐药性,目前已被公认为癌症治疗的主要靶点。在过去十年中,针对STAT3和STAT5的抑制剂研发一直是深入研究的课题。本综述总结了目前关于致癌性STAT3和STAT5在造血系统癌症中的功能知识,以及药理抑制剂在临床前和临床开发方面的进展。