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Epigenetics. 2016 May 3;11(5):344-53. doi: 10.1080/15592294.2016.1168673. Epub 2016 Apr 12.

Epigenetic and genetic burden measures are associated with tumor characteristics in invasive breast carcinoma.

Author information

1
a Department of Epidemiology , Geisel School of Medicine at Dartmouth.
2
b Department of Pharmacology and Toxicology , Geisel School of Medicine at Dartmouth , Hanover , NH , USA.
3
c Department of Biostatistics , University of Kansas Medical Center , Kansas City , KS , USA.
4
d Department of Community and Family Medicine , Geisel School of Medicine at Dartmouth , Lebanon , NH , USA.

Abstract

The development and progression of invasive breast cancer is characterized by alterations to the genome and epigenome. However, the relationship between breast tumor characteristics, disease subtypes, and patient outcomes with the cumulative burden of these molecular alterations are not well characterized. We determined the average departure of tumor DNA methylation from adjacent normal breast DNA methylation using Illumina 450K methylation data from 700 invasive breast tumors and 90 adjacent normal breast tissues in The Cancer Genome Atlas. From this we generated a novel summary measure of altered DNA methylation, the DNA methylation dysregulation index (MDI), and examined the relation of MDI with tumor characteristics and summary measures that quantify cumulative burden of genetic mutation and copy number alterations. Our analysis revealed that MDI was significantly associated with tumor stage (P = 0.017). Across invasive breast tumor subtypes we observed significant differences in genome-wide DNA MDIs (P = 4.9E-09) and in a fraction of the genome with copy number alterations (FGA) (P = 4.6E-03). Results from a linear regression adjusted for subject age, tumor stage, and estimated tumor purity indicated a positive significant association of MDI with both MCB and FGA (P = 0.036 and P < 2.2E-16). A recursively partitioned mixture model of all 3 somatic alteration burden measures resulted in classes of tumors whose epigenetic and genetic burden profile were associated with the PAM50 subtype and mutations in TP53, PIK3CA, and CDH1. Together, our work presents a novel framework for characterizing the epigenetic burden and adds to the understanding of the aggregate impact of epigenetic and genetic alterations in breast cancer.

KEYWORDS:

Breast cancer; DNA methylation; TCGA; deregulation; dysregulation; epigenome

PMID:
27070496
PMCID:
PMC4889287
DOI:
10.1080/15592294.2016.1168673
[Indexed for MEDLINE]
Free PMC Article

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