RT Journal Article SR Electronic T1 Whole genome methylation analysis of non-dysplastic Barretts oesophagus that progresses to invasive cancer JF bioRxiv FD Cold Spring Harbor Laboratory SP 114298 DO 10.1101/114298 A1 MP Dilworth A1 T Nieto A1 JD Stockton A1 C Whalley A1 L Tee A1 JD James A1 MT Hallissey A1 R Hejmadi A1 N Trugdill A1 O Tucker A1 AD Beggs YR 2017 UL http://biorxiv.org/content/early/2017/03/06/114298.abstract AB Objective To investigate differences in methylation between patients with non-dysplastic Barretts’ oesophagus who progress to invasive adenocarcinoma and those that do not.Design A whole genome methylation interrogation using the Illumina HumanMethylation 450 array of patients with non-dysplastic Barrett’s Oesophagus who either develop adenocarcinoma or remain static, with validation of findings by bisulfite pyrosequencingResults In total, 12 patients with “progressive” vs. 12 with “non-progressive” non-dysplastic Barrett’s oesophagus were analysed via methylation array. Fourty-four methylation markers were identified that may be able to discriminate between non-dysplastic Barrett’s Oesophagus that either progress to adenocarcinoma or remain static. Hypomethylation of the recently identified tumour supressor OR3A4 (probe cg09890332) validated in a separate cohort of samples (median methylation in progressors = 67.8% vs. 96.7% in non-progressors,p=0.0001, z = 3.85, Wilcoxon rank sum test) and was associated with the progression to adenocarcinoma. There were no differences in copy number between the two groups, but a global trend towards hypomethylation in the progressor group was observed.Conclusion Hypomethylation of OR3A4 has the ability to risk stratify the patient with non-dysplastic Barrett’s Oesophagus and may form the basis of a future surveillance program.