JAK2V617F/STAT5 signaling pathway promotes cell proliferation through activation of Pituitary Tumor Transforming Gene 1 expression

被引:10
作者
Shen, Xu-Liang [1 ,2 ]
Wei, Wu [2 ]
Xu, Hong-Liang [2 ]
Zhang, Mei-Xiang [2 ]
Qin, Xiao-Qi [2 ]
Shi, Wen-Zhi [2 ]
Jiang, Zhi-Ping [2 ]
Chen, Yi-Jian [3 ]
Chen, Fang-Ping [1 ]
机构
[1] Ctr S Univ, Xiangya Hosp, Dept Hematol, Changsha 410008, Hunan, Peoples R China
[2] Heping Hosp, Changzhi Med Coll, Dept Hematol, Changzhi 046000, Peoples R China
[3] GanNan Med Univ, Affiliated Hosp 1, Dept Hematol, Ganzhou 341000, Peoples R China
关键词
Myeloproliferative neoplasms; JAK2V617F; PTTG1; AG490; HEL cell; Proliferation; TYROSINE KINASE JAK2; ESSENTIAL THROMBOCYTHEMIA; POLYCYTHEMIA-VERA; ALLELE BURDEN; MUTATION; V617F; NEOPLASMS; MICE; PTTG; DIFFERENTIATION;
D O I
10.1016/j.bbrc.2010.07.005
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
Gain-of-function mutations of JAK2 play crucial roles in the development of myeloproliferative neoplasms; however, the underlying downstream events of this activated signaling pathway are not fully understood. Our experiment was designed and performed to address one aspect of this issue. Here we report that AG490, a potent JAK2V617F kinase inhibitor, effectively inhibits the proliferation of HEL cells. Interestingly, AG490 also decreases the expression of PITG1, a possible target gene of the aberrant signaling pathway, in a dose- and time-dependent manner. Furthermore, the promoter activity analyses reveal that the inhibition of the PTTG1 expression is affected at the transcriptional level. Thus, our results suggest that the JAK2V617F/STAT5 signaling pathway promotes cell proliferation through the transcriptional activation of PTTG1. (c) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:707 / 712
页数:6
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