Epigenetic landscape correlates with genetic subtype but does not predict outcome in childhood acute lymphoblastic leukemia

Gabriel, Alem, Lafta, Fadhel, Schwalbe, Ed, Nakjang, Sirintra, Cockell, Simon, Iliasova, Alice, Enshaei, Amir, Schwab, Claire, Rand, Vikki, Clifford, Steven, Kinsey, Sally, Mitchell, Chris, Vora, Ajay, Harrison, Christine, Moorman, Anthony and Strathdee, Gordon (2015) Epigenetic landscape correlates with genetic subtype but does not predict outcome in childhood acute lymphoblastic leukemia. Epigenetics, 10 (8). pp. 717-726. ISSN 1559-2294

Epigenetic landscape.pdf - Published Version
Available under License Creative Commons Attribution.

Download (747kB) | Preview
Official URL: http://dx.doi.org/10.1080/15592294.2015.1061174


Although children with acute lymphoblastic leukemia (ALL) generally have a good outcome, some patients do relapse and survival following relapse is poor. Altered DNA methylation is highly prevalent in ALL and raises the possibility that DNA methylation-based biomarkers could predict patient outcome. In this study, genome-wide methylation analysis, using the Illumina Infinium HumanMethylation450 BeadChip platform, was carried out on 52 diagnostic patient samples from 4 genetic subtypes [ETV6-RUNX1, high hyperdiploidy (HeH), TCF3-PBX1 and dic(9;20)(p11–13;q11)] in a 1:1 case-control design with patients who went on to relapse (as cases) and patients achieving long-term remission (as controls). Pyrosequencing assays for selected loci were used to confirm the array-generated data. Non-negative matrix factorization consensus clustering readily clustered samples according to genetic subgroups and gene enrichment pathway analysis suggested that this is in part driven by epigenetic disruption of subtype specific signaling pathways. Multiple bioinformatics approaches (including bump hunting and individual locus analysis) were used to identify CpG sites or regions associated with outcome. However, no associations with relapse were identified. Our data revealed that ETV6-RUNX1 and dic(9;20) subtypes were mostly associated with hypermethylation; conversely, TCF3-PBX1 and HeH were associated with hypomethylation. We observed significant enrichment of the neuroactive ligand-receptor interaction pathway in TCF3-PBX1 as well as an enrichment of genes involved in immunity and infection pathways in ETV6-RUNX1 subtype. Taken together, our results suggest that altered DNA methylation may have differential impacts in distinct ALL genetic subtypes.

Item Type: Article
Uncontrolled Keywords: 450K, ALL, biomarker, childhood, methylation, relapse
Subjects: B100 Anatomy, Physiology and Pathology
Department: Faculties > Health and Life Sciences > Applied Sciences
Depositing User: Becky Skoyles
Date Deposited: 04 Sep 2015 11:42
Last Modified: 01 Aug 2021 06:01
URI: http://nrl.northumbria.ac.uk/id/eprint/23693

Actions (login required)

View Item View Item


Downloads per month over past year

View more statistics