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BAALC and ERG expression levels are associated with outcome and distinct gene and microRNA expression profiles in older patients with de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study.

Authors :
Schwind S
Marcucci G
Maharry K
Radmacher MD
Mrózek K
Holland KB
Margeson D
Becker H
Whitman SP
Wu YZ
Metzeler KH
Powell BL
Kolitz JE
Carter TH
Moore JO
Baer MR
Carroll AJ
Caligiuri MA
Larson RA
Bloomfield CD
Source :
Blood [Blood] 2010 Dec 16; Vol. 116 (25), pp. 5660-9. Date of Electronic Publication: 2010 Sep 14.
Publication Year :
2010

Abstract

BAALC and ERG expression levels are prognostic markers in younger (< 60 years) cytogenetically normal acute myeloid leukemia (CN-AML) adults; their prognostic impact in older (≥ 60 years) patients requires further investigation. We evaluated pretreatment expression of BAALC and ERG in 158 de novo patients treated on cytarabine/daunorubicin-based protocols. The patients were also characterized for other established molecular prognosticators. Low BAALC and ERG expression levels were associated with better outcome in univariable and multivariable analyses. Expression levels of both BAALC and ERG were the only factors significantly associated with overall survival upon multivariable analysis. To gain biological insights, we derived gene expression signatures associated with BAALC and ERG expression in older CN-AML patients. Furthermore, we derived the first microRNA expression signatures associated with the expression of these 2 genes. In low BAALC expressers, genes associated with undifferentiated hematopoietic precursors and unfavorable outcome predictors were down-regulated, whereas HOX genes and HOX-gene-embedded microRNAs were up-regulated. Low ERG expressers presented with down-regulation of genes involved in the DNA-methylation machinery, and up-regulation of miR-148a, which targets DNMT3B. We conclude that in older CN-AML patients, low BAALC and ERG expression associates with better outcome and distinct gene and microRNA expression signatures that could aid in identifying new targets and novel therapeutic strategies for older patients.

Details

Language :
English
ISSN :
1528-0020
Volume :
116
Issue :
25
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
20841507
Full Text :
https://doi.org/10.1182/blood-2010-06-290536