生物
转录因子
髓系白血病
白血病
增强子
同源盒
癌症研究
基因
基因表达调控
转化(遗传学)
髓样
细胞生物学
遗传学
干细胞
造血
作者
Carmel T Collins,Jay L. Hess
出处
期刊:Oncogene
[Springer Nature]
日期:2015-06-01
卷期号:35 (9): 1090-1098
被引量:135
摘要
HOXA9 is a homeodomain-containing transcription factor that has an important role in hematopoietic stem cell expansion and is commonly deregulated in acute leukemias. A variety of upstream genetic alterations in acute myeloid leukemia lead to overexpression of HOXA9, which is a strong predictor of poor prognosis. In many cases, HOXA9 has been shown to be necessary for maintaining leukemic transformation; however, the molecular mechanisms through which it promotes leukemogenesis remain elusive. Recent work has established that HOXA9 regulates downstream gene expression through binding at promoter distal enhancers along with a subset of cell-specific cofactor and collaborator proteins. Increasing efforts are being made to identify both the critical cofactors and target genes required for maintaining transformation in HOXA9-overexpressing leukemias. With continued advances in understanding HOXA9-mediated transformation, there is a wealth of opportunity for developing novel therapeutics that would be applicable for greater than 50% of AML with overexpression of HOXA9.
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