4.7 Editorial Material

Fingerprinting Acute Leukemia: DNA Methylation Profiling of B-Acute Lymphoblastic Leukemia

Journal

CANCER DISCOVERY
Volume 2, Issue 11, Pages 976-978

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/2159-8290.CD-12-0435

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Funding

  1. Howard Hughes Medical Institute Funding Source: Medline
  2. NCI NIH HHS [R01 CA133379, R01CA133379, R01 CA149655, R01 CA105129, R01CA149655, R01CA105129, R01 CA169784, R01 CA173636] Funding Source: Medline
  3. NIGMS NIH HHS [R01GM088847, R01 GM088847] Funding Source: Medline

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In this issue of Cancer Discovery, Geng and colleagues report on their use of a combination of promoter cytosine methylation profiling with gene expression and ChIP sequencing to elucidate molecular signatures of adult B-acute lymphoblastic leukemia patient samples with BCR-ABL1, E2A-PBX1, and MLL rearrangements. The unique epigenetic and gene expression signatures of these clinically unfavorable B-ALL subtypes identify novel biomarkers and provide a strong rationale for repurposing existing therapies to treat these molecularly distinct diseases. Cancer Discov; 2(11); 976-8. (C) 2012 AACR. Commentary on Geng et al., p. 1004 (4).

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