Signal transducer and activator of transcription (STAT)-5: an opportunity for drug development in oncohematology

状态5 STAT蛋白 斯达 生物 JAK-STAT信号通路 癌症研究 车站3 STAT1 造血 状态4 信号转导 转录因子 贾纳斯激酶 癌变 细胞生物学 STAT6 抄写(语言学) 酪氨酸激酶 免疫学 激活剂(遗传学) 免疫系统 基因 干细胞 遗传学 白细胞介素4
作者
Carlota Recio,Borja Guerra,Miguel Guerra-Rodríguez,Haidée Aranda-Tavío,Patricia Martín-Rodríguez,Mercedes de Mirecki-Garrido,Yeray Brito‐Casillas,José Manuel García-Castellano,Ana Estévez‐Braun,Leandro Fernández-Pérez
出处
期刊:Oncogene [Springer Nature]
卷期号:38 (24): 4657-4668 被引量:23
标识
DOI:10.1038/s41388-019-0752-3
摘要

The signal transducer and activator of transcription (STAT) are transcription factors that work via JAK/STAT pathway regulating the expression of genes involved in cell survival, proliferation, differentiation, development, immune response, and, among other essential biological functions, hematopoiesis. JAK/STAT signaling is strictly regulated under normal physiological conditions. However, a large group of diverse diseases has been associated to an aberrant regulation of STAT factors. Erroneous modulation of the pathway leads to constitutive STAT activation, thereby driving proliferation, inflammation, and an uncontrolled immune response. Deregulated STAT5 activation has been found in the development of many hematopoietic tumors, including chronic and acute leukemias, polycythemia vera, and lymphoma. Mutations in the kinases that phosphorylate STAT5, and/or overexpression of the upstream receptor-associated tyrosine kinases have been suggested as the main drivers of constitutive STAT5 activation. Hyper-activated STAT5 leads to the aberrant expression of its target genes including antiapoptotic, proliferative, and pro-inflammatory genes, favouring tumorigenesis. In this review, we intent to discuss the biology of JAK/STAT pathway, with particular focus on STAT5 and its crucial role in the development and progression of hematologic malignancies. Furthermore, we provide a synopsis of potential therapeutic strategies based on STAT5 activity inhibition that may represent an excellent opportunity for drug development in oncohematology.
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