Aberrant let7a/HMGA2 signaling activity with unique clinical phenotype in JAK2-mutated myeloproliferative neoplasms

Chih Cheng Chen, Jie Yu You, Jrhau Lung, Cih En Huang, Yi Yang Chen, Yu Wei Leu, Hsing Ying Ho, Chian Pei Li, Chang Hsien Lu, Kuan Der Lee, Chia Chen Hsu, Jyh Pyng Gau

研究成果: 雜誌貢獻文章

5 引文 斯高帕斯(Scopus)

摘要

High mobility group AT-hook 2 (HMGA2) is an architectural transcription factor that is negatively regulated by let-7 microRNA through binding to it’s 3’-untranslated region. Transgenic mice expressing Hmga2 with a truncation of its 3’-untranslated region has been shown to exhibit a myeloproliferative phenotype. To decipher the let-7-HMGA2 axis in myeloproliferative neoplasms, we employed an in vitro model supplemented with clinical correlation. Ba/F3 cells with inducible JAK2V617F expression (Ton.JAK2.V617F cells) showed upregulation of HMGA2 with concurrent let-7a repression. Ton.JAK2.V617F cells treated with a let-7a inhibitor exhibited further escalation of Hmga2 expression, while a let-7a mimic diminished the Hmga2 transcript level. Hmga2 overexpression conferred JAK2-mutated cells with a survival advantage through inhibited apoptosis. A pan-JAK inhibitor, INC424, increased the expression of let-7a, downregulated the level of Hmga2, and led to increased apoptosis in Ton.JAK2.V617F cells in a dose-dependent manner. In samples from 151 patients with myeloproliferative neoplasms, there was a modest inverse correlation between the expression levels of let-7a and HMGA2. Overexpression of HMGA2 was detected in 29 (19.2%) of the cases, and it was more commonly seen in patients with essential thrombocythemia than in those with polycythemia vera (26.9% vs. 12.7%, P=0.044). Patients with upregulated HMGA2 showed an increased propensity for developing major thrombotic events, and they were more likely to harbor one of the 3 driver myeloproliferative neoplasm mutations in JAK2, MPL and CALR. Our findings suggest that, in a subset of myeloproliferative neoplasm patients, the let-7-HMGA2 axis plays a prominent role in the pathogenesis of the disease that leads to unique clinical phenotypes.
原文英語
頁(從 - 到)509-518
頁數10
期刊Haematologica
102
發行號3
DOIs
出版狀態已發佈 - 二月 28 2017
對外發佈Yes

ASJC Scopus subject areas

  • Hematology

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    Chen, C. C., You, J. Y., Lung, J., Huang, C. E., Chen, Y. Y., Leu, Y. W., Ho, H. Y., Li, C. P., Lu, C. H., Lee, K. D., Hsu, C. C., & Gau, J. P. (2017). Aberrant let7a/HMGA2 signaling activity with unique clinical phenotype in JAK2-mutated myeloproliferative neoplasms. Haematologica, 102(3), 509-518. https://doi.org/10.3324/haematol.2016.154385