Genome-wide methylation analysis identifies genes specific to breast cancer hormone receptor status and risk of recurrence.

Journal Article (Journal Article)

To better understand the biology of hormone receptor-positive and-negative breast cancer and to identify methylated gene markers of disease progression, we carried out a genome-wide methylation array analysis on 103 primary invasive breast cancers and 21 normal breast samples, using the Illumina Infinium HumanMethylation27 array that queried 27,578 CpG loci. Estrogen and/or progesterone receptor-positive tumors displayed more hypermethylated loci than estrogen receptor (ER)-negative tumors. However, the hypermethylated loci in ER-negative tumors were clustered closer to the transcriptional start site compared with ER-positive tumors. An ER-classifier set of CpG loci was identified, which independently partitioned primary tumors into ER subtypes. A total of 40 (32 novel and 8 previously known) CpG loci showed differential methylation specific to either ER-positive or ER-negative tumors. Each of the 40 ER subtype-specific loci was validated in silico, using an independent, publicly available methylome dataset from the Cancer Genome Atlas. In addition, we identified 100 methylated CpG loci that were significantly associated with disease progression; the majority of these loci were informative particularly in ER-negative breast cancer. Overall, the set was highly enriched in homeobox containing genes. This pilot study shows the robustness of the breast cancer methylome and illustrates its potential to stratify and reveal biological differences between ER subtypes of breast cancer. Furthermore, it defines candidate ER-specific markers and identifies potential markers predictive of outcome within ER subgroups.

Full Text

Duke Authors

Cited Authors

  • Fackler, MJ; Umbricht, CB; Williams, D; Argani, P; Cruz, L-A; Merino, VF; Teo, WW; Zhang, Z; Huang, P; Visvananthan, K; Marks, J; Ethier, S; Gray, JW; Wolff, AC; Cope, LM; Sukumar, S

Published Date

  • October 1, 2011

Published In

Volume / Issue

  • 71 / 19

Start / End Page

  • 6195 - 6207

PubMed ID

  • 21825015

Pubmed Central ID

  • PMC3308629

Electronic International Standard Serial Number (EISSN)

  • 1538-7445

Digital Object Identifier (DOI)

  • 10.1158/0008-5472.CAN-11-1630


  • eng

Conference Location

  • United States