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

被引:33
|
作者
Recio, Carlota [1 ]
Guerra, Borja [1 ]
Guerra-Rodriguez, Miguel [1 ]
Aranda-Tavio, Haidee [1 ]
Martin-Rodriguez, Patricia [1 ]
de Mirecki-Garrido, Mercedes [1 ]
Brito-Casillas, Yeray [1 ]
Garcia-Castellano, Jose M. [1 ]
Estevez-Braun, Ana [2 ]
Fernandez-Perez, Leandro [1 ]
机构
[1] Univ Las Palmas Gran Canaria, IUIBS, Farmacol Mol & Traslac BIOPharm, Las Palmas De Gc 35016, Las Palmas, Spain
[2] Univ La Laguna, Inst Univ Bioorgan CIBICAN, Dept Quim Organ, E-38206 Tenerife, Spain
关键词
CHRONIC MYELOID-LEUKEMIA; HODGKIN LYMPHOMA; JANUS KINASES; STAT PROTEINS; SELF-RENEWAL; BCR-ABL; CELLS; IMATINIB; MUTATION; PATHWAY;
D O I
10.1038/s41388-019-0752-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:4657 / 4668
页数:12
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