DNA methylation and obesity in survivors of pediatric acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study.
Philip J LupoAustin L BrownVidal M ArroyoKala Y KamdarJohn W BelmontMichael E ScheurerWendy M LeisenringM. Monica GramatgesM. Fatih OkcuYutaka YasuiKevin C OeffingerLeslie L RobisonGregory T ArmstrongSmita BhatiaPublished in: Genes, chromosomes & cancer (2018)
Because survivors of pediatric acute lymphoblastic leukemia (ALL) are more likely to be obese than unaffected contemporaries, we compared DNA methylation profiles between normal-weight and obese survivors at adiposity-associated CpG sites previously-reported by epigenome-wide association studies (EWAS) of body mass index (BMI) in the general population. We selected 96 ALL survivors from the Childhood Cancer Survivor Study: 48 obese and 48 normal weight. The Illumina HumanMethylation450 BeadChip was used to compare DNA methylation at 211 loci identified in EWAS of BMI in the general population. Thirty-nine loci were associated (false discovery rate <0.05) with obesity among survivors who only received chemotherapy (n = 49). No loci were significantly associated with obesity among CRT-exposed survivors (n = 47). Our results suggest that previously identified BMI-DNA methylation loci are associated with obesity in ALL survivors who were spared CRT, while no loci were significantly associated with obesity in survivors who received CRT.
Keyphrases
- dna methylation
- weight loss
- weight gain
- genome wide
- young adults
- body mass index
- childhood cancer
- metabolic syndrome
- insulin resistance
- acute lymphoblastic leukemia
- type diabetes
- bariatric surgery
- gene expression
- adipose tissue
- high fat diet induced
- copy number
- genome wide association study
- small molecule
- genome wide association
- heart failure
- cardiac resynchronization therapy
- squamous cell carcinoma
- obese patients
- left ventricular
- allogeneic hematopoietic stem cell transplantation
- high throughput