Specific hypomethylated CpGs at the IGF2 locus act as an epigenetic biomarker for familial adenomatous polyposis colorectal cancer.

The identification of specific biomarkers for colorectal cancer is of primary importance for early diagnosis. The aim of this study was to evaluate if methylation changes at the IGF2/H19 locus could be predictive for individuals at high risk for developing sporadic or hereditary colorectal cancer.
Quantitative methylation analysis using pyrosequencing was performed on three differentially methylated regions (DMRs): IGF2 DMR0 and DMR2 and the H19 DMR in DNA samples from sporadic colorectal cancer (n = 26), familial adenomatous polyposis (n = 35) and hereditary nonpolyposis colorectal cancer (n = 19) patients.
We report in this article for the first time, that in sporadic colorectal cancer tumor DNA both the IGF2 DMR0 and DMR2 are hypomethylated, while the H19 DMR retains its monoallelic methylation pattern. In lymphocyte DNA, a striking hypomethylation of nine contiguous correlated CpGs was found in the IGF2 DMR2 but only in familial adenomatous polyposis patients.
Methylation alterations at the IGF2 locus are more extensive than previously reported and DMR2 hypomethylation in lymphocyte DNA might be a specific epigenetic biomarker for familial adenomatous polyposis patients.
AuthorsAudrey Miroglio, Hélène Jammes, Jörg Tost, Loïc Ponger, Ivo Glynne Gut, Hafida El Abdalaoui, Joël Coste, Stanislas Chaussade, Paola B Arimondo, Dominique Lamarque, Luisa Dandolo
JournalEpigenomics (Epigenomics) Vol. 2 Issue 3 Pg. 365-75 (Jun 2010) ISSN: 1750-192X [Electronic] England
PMID22121898 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers
  • IGF2 protein, human
  • Sulfites
  • Insulin-Like Growth Factor II
  • hydrogen sulfite
  • Adenomatous Polyposis Coli (metabolism)
  • Biomarkers (metabolism)
  • Cluster Analysis
  • Colorectal Neoplasms (metabolism)
  • CpG Islands (genetics)
  • DNA Methylation (genetics)
  • France
  • Humans
  • Insulin-Like Growth Factor II (genetics)
  • Lymphocytes (metabolism)
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA (methods)
  • Sulfites

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