Molecular Taxonomy of Pediatric Cancer
OBJECTIVES:
- To identify global changes in the epigenome and various underlying histone
modifications that characterize relapsed acute lymphoblastic leukemia (ALL).
- To identify specific transcription factor-binding sites associated with histone
alterations.
- To correlate gene expression changes of differentially regulated genes at relapse with
underlying chromatin modifications.
OUTLINE: Archived bone marrow samples, collected at the time of diagnosis and relapse, are
analyzed for gene expression and histone modifications by microarray, chromatin
immunoprecipitation (ChIP) sequencing, and quantitative real-time polymerase chain reaction
(qRT-PCR).
Observational
N/A
Cellular origins of relapse and the underlying epigenetic mechanisms associated with drug resistance
No
William L. Carroll, MD
Principal Investigator
NYU Clinical Cancer Center
United States: Federal Government
CDR0000735342
NCT01625143
June 2012
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