A systematic review of epigenetic biomarkers in progression from non-dysplastic Barrett's oesophagus to oesophageal adenocarcinoma

被引:7
|
作者
Nieto, Tom [1 ]
Tomlinson, Claire L. [2 ]
Dretzke, Janine [3 ]
Bayliss, Susan [3 ]
Price, Malcolm James [3 ]
Dilworth, Mark [4 ,5 ]
Beggs, Andrew D. [1 ]
Tucker, Olga [1 ,4 ,5 ]
机构
[1] Univ Birmingham, Dept Surg, Birmingham, W Midlands, England
[2] Univ Birmingham, Inst Appl Hlth Res, Birmingham Clin Trials Unit, Birmingham, W Midlands, England
[3] Univ Birmingham, Inst Appl Hlth Res, Birmingham, W Midlands, England
[4] Univ Birmingham, Heart England Fdn Trust, Dept Surg, Birmingham, W Midlands, England
[5] Univ Birmingham, Inst Inflammat & Ageing, Birmingham, W Midlands, England
来源
BMJ OPEN | 2018年 / 8卷 / 06期
关键词
SQUAMOUS-CELL CARCINOMA; HIGH-GRADE DYSPLASIA; NEOPLASTIC PROGRESSION; PROMOTER METHYLATION; ABERRANT METHYLATION; P16; GENE; CANCER; HYPERMETHYLATION; DISEASE; METAANALYSIS;
D O I
10.1136/bmjopen-2017-020427
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The objective of this systematic review is to identify and summarise studies which examine epigenetic biomarkers in patients with Barrett's oesophagus (BO) and their association with progression to oesophageal adenocarcinoma (OADC). BO is a precursor lesion for OADC. There is no clinical test to predict patients who are likely to progress to OADC. An epigenetic biomarker could predict patients who are at high risk of progression from BO to OADC which could facilitate earlier diagnosis and spare those unlikely to develop cancer from regular invasive surveillance endoscopy. Setting A systematic search was conducted of the following databases: MEDLINE, MEDLINE in Process, EMBASE, Cochrane Central, ISI Conference Proceedings Citation Index and the British Library's ZETOC. Studies were conducted in secondary and tertiary care settings. Participants All studies measuring epigenetic change in patients over 18 years old who progressed from non-dysplastic 80 to OADC were included. Genetic, in vitro and studies which did not measure progression in the same patient cohort were excluded. Study inclusion and risk of bias of individual eligible studies were assessed in duplicate by two reviewers using a modified Quality in Prognostic Studies tool. Results 14 studies met the inclusion criteria. 42 epigenetic markers were identified, and 5 studies developed models aiming to predict progression to OADC. Conclusions The evidence from this systematic review is suggestive of a role for p16 as an epigenetic biomarker for the progression of BO to OADC.
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页数:14
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