共 167 条
Role of HOXA9 in leukemia: dysregulation, cofactors and essential targets
被引:137
作者:

Collins, C. T.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA

Hess, J. L.
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h-index: 0
机构:
Indiana Univ, Sch Med, Dept Pathol & Lab Med, 340 West 10th St, Indianapolis, IN 46202 USA
Indiana Univ, Sch Med, Dept Med, 340 West 10th St, Indianapolis, IN 46202 USA Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
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
来源:
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.
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页码:1090 / 1098
页数:9
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Univ Cambridge, MRC Cambridge Stem Cell Inst, Cambridge Inst Med Res, Cambridge CB2 0XY, England Univ Cambridge, Dept Haematol, Wellcome Trust, Cambridge CB2 0XY, England

Gottgens, B.
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Univ Cambridge, Dept Haematol, Wellcome Trust, Cambridge CB2 0XY, England
Univ Cambridge, MRC Cambridge Stem Cell Inst, Cambridge Inst Med Res, Cambridge CB2 0XY, England Univ Cambridge, Dept Haematol, Wellcome Trust, Cambridge CB2 0XY, England