SwePub
Sök i LIBRIS databas

  Extended search

onr:"22086874"
 

Search: onr:"22086874" > Genome-wide signatu...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia

Nordlund, Jessica (author)
Backlin, Christofer L. (author)
Wahlberg, Per (author)
show more...
Busche, Stephan (author)
Berglund, Eva C. (author)
Eloranta, Maija-Leena (author)
Flaegstad, Trond (author)
Forestier, Erik (author)
Frost, Britt-Marie (author)
Harila-Saari, Arja (author)
Heyman, Mats (author)
Jonsson, Olafur G. (author)
Larsson, Rolf (author)
Palle, Josefine (author)
Ronnblom, Lars (author)
Schmiegelow, Kjeld (author)
Sinnett, Daniel (author)
Soderhall, Stefan (author)
Pastinen, Tomi (author)
Gustafsson, Mats G. (author)
Lonnerholm, Gudmar (author)
Syvanen, Ann-Christine (author)
show less...
 (publisher)
BioMed Central 2013
2013
English.
In: Genome Biology. - 1465-6906. ; 14:9, Article number: r105
  • swepub:Mat__t
Abstract Subject headings
Close  
  • Background: Although aberrant DNA methylation has been observed previously in acute lymphoblastic leukemia (ALL), the patterns of differential methylation have not been comprehensively determined in all subtypes of ALL on a genome-wide scale. The relationship between DNA methylation, cytogenetic background, drug resistance and relapse in ALL is poorly understood. Results: We surveyed the DNA methylation levels of 435,941 CpG sites in samples from 764 children at diagnosis of ALL and from 27 children at relapse. This survey uncovered four characteristic methylation signatures. First, compared with control blood cells, the methylomes of ALL cells shared 9,406 predominantly hypermethylated CpG sites, independent of cytogenetic background. Second, each cytogenetic subtype of ALL displayed a unique set of hyper- and hypomethylated CpG sites. The CpG sites that constituted these two signatures differed in their functional genomic enrichment to regions with marks of active or repressed chromatin. Third, we identified subtype-specific differential methylation in promoter and enhancer regions that were strongly correlated with gene expression. Fourth, a set of 6,612 CpG sites was predominantly hypermethylated in ALL cells at relapse, compared with matched samples at diagnosis. Analysis of relapse-free survival identified CpG sites with subtype-specific differential methylation that divided the patients into different risk groups, depending on their methylation status. Conclusions: Our results suggest an important biological role for DNA methylation in the differences between ALL subtypes and in their clinical outcome after treatment.

Subject headings

Medical and Health Sciences  (hsv)
Basic Medicine  (hsv)
Medical Genetics  (hsv)
Medicin och hälsovetenskap  (hsv)
Medicinska grundvetenskaper  (hsv)
Medicinsk genetik  (hsv)
Medical and Health Sciences  (hsv)
Basic Medicine  (hsv)
Microbiology in the medical area  (hsv)
Medicin och hälsovetenskap  (hsv)
Medicinska grundvetenskaper  (hsv)
Mikrobiologi inom det medicinska området  (hsv)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view