Role of HOXA9 in leukemia: dysregulation, cofactors and essential targets

被引:137
作者
Collins, C. T. [1 ]
Hess, J. L. [2 ,3 ]
机构
[1] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Indiana Univ, Sch Med, Dept Pathol & Lab Med, 340 West 10th St, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Med, 340 West 10th St, Indianapolis, IN 46202 USA
关键词
ACUTE MYELOID-LEUKEMIA; LONG NONCODING RNA; HEMATOPOIETIC STEM-CELLS; BONE-MARROW-CELLS; ACUTE MYELOGENOUS LEUKEMIA; GENE-EXPRESSION PATTERN; MIXED-LINEAGE LEUKEMIA; HOMEOBOX-GENE; TRANSCRIPTION FACTORS; POOR-PROGNOSIS;
D O I
10.1038/onc.2015.174
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
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.
引用
收藏
页码:1090 / 1098
页数:9
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