Evidence map›Paper›PMID 26545406›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2015

Methylated B3GAT2 and ZNF793 Are Potential Detection Biomarkers for Barrett's Esophagus.

Ming Yu, Rachele M O'Leary, Andrew M Kaz, Shelli M Morris, Kelly T Carter, Amitabh Chak, Apoorva Chandar, Joseph E Willis, Helen R Moinova, Sanford D Markowitz and 8 more

Open access · greenAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Novel DNA Methylation Biomarker Panel for Detection of Esophageal Adenocarcinoma and High-Grade Dysplasia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. Barrett's Esophagus and Esophageal Adenocarcinoma Biomarkers.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Article
  9. Article
  10. Review
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 7 institutions in 1 country.

Ming YuDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Rachele M O'LearyDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Andrew M KazResearch and Development Service, VA Puget Sound Health Care System, Seattle, Washington. Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Shelli M MorrisDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Kelly T CarterDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Amitabh ChakDivision of Gastroenterology, University Hospitals Case Medical Center, Cleveland, Ohio. Division of Oncology, University Hospitals Case Medical Center, Cleveland, Ohio.
Apoorva ChandarDivision of Gastroenterology, University Hospitals Case Medical Center, Cleveland, Ohio. Division of Oncology, University Hospitals Case Medical Center, Cleveland, Ohio.
Joseph E WillisDepartment of Pathology, University Hospitals Case Medical Center, Cleveland, Ohio.
Helen R MoinovaDepartment of Medicine, University Hospitals Case Medical Center, Cleveland, Ohio.
Sanford D MarkowitzDepartment of Medicine, University Hospitals Case Medical Center, Cleveland, Ohio. Case Comprehensive Cancer Center, Case Western Reserve University, School of Medicine, Cleveland, Ohio.
Dean E BrennerUniversity of Michigan Medical Center, Ann Arbor, Michigan.
Sharmila AnandabapasathyDepartment of Medicine and Gastroenterology, Baylor College of Medicine, Houston, Texas.
Maria WesterhoffDepartment of Anatomic Pathology, University of Washington School of Medicine, Seattle, Washington.
Chao-Jen WongDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Nicholas J ShaheenDivision of Gastroenterology & Hepatology, University of North Carolina Hospitals, Chapel Hill, North Carolina.
Yanwen ChenCase Comprehensive Cancer Center, Case Western Reserve University, School of Medicine, Cleveland, Ohio.
Jill S Barnholtz-SloanCase Comprehensive Cancer Center, Case Western Reserve University, School of Medicine, Cleveland, Ohio.
William M GradyDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington. Department of Medicine, University of Washington School of Medicine, Seattle, Washington. wgrady@fredhutch.org.
Fred Hutch Cancer Center · USUniversity Hospitals Cleveland Medical Center · USUniversity of Washington · USCase Western Reserve University · USBaylor College of Medicine · USUniversity of Michigan · USUniversity of North Carolina Hospitals · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
SAN ANTONIO CENTER OF BIOMARKERS OF RISK FOR PROSTATE CAU01CA086402 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LEACH, ROBIN JEAN, THOMPSON, IAN M. · 2000 to 2018
$33.1M
Great Lakes/New England Clinical Validation CenterU01CA086400 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICCIARDIELLO, LUIGI, SYNGAL, SAPNA · 2000 to 2025
$26.0M
Targeting 15-PGDH in Colon Cancer Prognosis, Prediction, Treatment and PreventionP50CA150964 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARKOWITZ, SANFORD D. · 2011 to 2022
$24.6M
The Cleveland Digestive Diseases Research Core Center (DDRCC)P30DK097948 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI Theresa Torres Pizarro · 2015 to 2026
$15.6M
Whole Exome Approaches for Esophageal Adenocarcinoma Susceptibility GenesU54CA163060 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI CHAK, AMITABH, GUDA, KISHORE · 2011 to 2022
$14.0M
Identify and validate novel epigenetic molecular markers for colorectal neoplasmU01CA152756 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GRADY, WILLIAM MALLORY, GUDA, KISHORE · 2010 to 2021
$6.7M
UNIVERSITY OF WASHINGTON GI TRAINING GRANTT32DK007742 · NIDDK · UNIVERSITY OF WASHINGTON · PI GRADY, WILLIAM MALLORY · 1996 to 2022
$4.7M
Esophageal Cancer from Cells to Population: A Multiscale ApproachU01CA182940 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HUR, CHIN, INADOMI, JOHN MATTHEW · 2013 to 2017
$3.3M
Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative TherapyK24DK100548 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SHAHEEN, NICHOLAS J · 2013 to 2017
$896k
NCI NIH HHS 5P30CA015704NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA150964NCI NIH HHS P50CA150964NCI NIH HHS U01 CA086400NCI NIH HHS U01 CA086402NCI NIH HHS U01CA086402NCI NIH HHS U01 CA152756NCI NIH HHS U01 CA182940NCI NIH HHS U01CA182940NCI NIH HHS U01CA86400NCI NIH HHS U54 CA163060NCI NIH HHS U54CA163060NCI NIH HHS UO1 CA152756NIDDK NIH HHS K24 DK100548NIDDK NIH HHS P30 DK097948NIDDK NIH HHS T32 DK007742NIDDK NIH HHS T32DK007742
6 · The paper itself

Abstract

backgroundBarrett's esophagus (BE) is a preneoplastic condition in which normal esophageal squamous epithelium (SQ) is replaced by specialized intestinal metaplasia. It is the presumed precursor for esophageal adenocarcinoma (EAC) as well as the strongest risk factor for this cancer. Unfortunately, many patients with BE go undiagnosed under the current BE screening guidelines. The development of noninvasive and accurate BE detection assays could potentially identify many of these undiagnosed BE patients.

methodsDNA methylation is a common epigenetic alteration in BE. Therefore, we conducted a genome-wide methylation screen to identify potential BE biomarkers. Samples from SQ (N = 12), stomach (N = 28), and BE (N = 29) were analyzed and methylation levels at over 485,000 CpG sites were compared. Pyrosequencing assays were used to validate the results and MethyLight assays were developed to detect the methylated alleles in endoscopic brushings.

resultsWe discovered two genes, B3GAT2 and ZNF793, that are aberrantly methylated in BE. Clinical validation studies confirmed B3GAT2 and ZNF793 methylation levels were significantly higher in BE samples (median = 32.5% and 33.1%, respectively) than in control tissues (median = 2.29% and 2.52%, respectively; P < 0.0001 for both genes). Furthermore, gene-specific MethyLight assays could accurately detect BE (P < 0.0001 for both) in endoscopic brushing samples.

conclusionB3GAT2 and ZNF793 are hypermethylated in BE, and the methylation status of these genes can be used to detect BE in tissue samples. IMPACT: These findings support the development of methylated B3GAT2 and ZNF793 as biomarkers for noninvasive assays for the detection of BE.

Indexed as

DNA MethylationBarrett EsophagusBiomarkers, TumorGlucuronosyltransferaseHumansZinc FingersB3GAT2 protein, humanBiomarkers, TumorGlucuronosyltransferase

Identifiers

PMID26545406
PMCPMC4670566
OpenAlexW2112659260

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.