Evidence map›Paper›PMID 26068095›Full record

ArticleThe Journal of molecular diagnostics : JMD2015

Evaluation of Mutational Testing of Preneoplastic Barrett's Mucosa by Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Endoscopic Samples for Detection of Concurrent Dysplasia and Adenocarcinoma in Barrett's Esophagus.

Armando Del Portillo, Stephen M Lagana, Yuan Yao, Takeshi Uehara, Nirag Jhala, Tapan Ganguly, Peter Nagy, Jorge Gutierrez, Aesis Luna, Julian Abrams and 5 more

Open access · bronzeAbstract readComparative StudyEvaluation Study
In one paragraph

Article in The Journal of molecular diagnostics : JMD, 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
2.7field-weighted citation impact, top 11% 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, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. A Tissue Systems Pathology Test Detects Abnormalities Associated with Prevalent High-Grade Dysplasia and Esophageal Cancer in Barrett's Esophagus.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2017
    Article
  8. Article
  9. Review
  10. Review
  11. A Tissue Systems Pathology Assay for High-Risk Barrett's Esophagus.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2016
    Article
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

15 authors at 4 institutions in 2 countries.

Armando Del PortilloDepartment of Pathology and Cell Biology, Columbia University, New York City, New York.
Stephen M LaganaDepartment of Pathology and Cell Biology, Columbia University, New York City, New York.
Yuan YaoDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Takeshi UeharaDepartment of Pathology, Shinshu University, Nagano, Japan.
Nirag JhalaDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Tapan GangulyDepartment of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania.
Peter NagyDepartment of Pathology and Cell Biology, Columbia University, New York City, New York.
Jorge GutierrezDepartment of Pathology and Cell Biology, Columbia University, New York City, New York.
Aesis LunaDepartment of Pathology and Cell Biology, Columbia University, New York City, New York.
Julian AbramsDivision of Gastroenterology, Columbia University, New York City, New York.
Yang LiuDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Randall BrandDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Jorge L SepulvedaDepartment of Pathology and Cell Biology, Columbia University, New York City, New York.
Gary W FalkDivision of Gastroenterology, University of Pennsylvania, Philadelphia, Pennsylvania.
Antonia R SepulvedaDepartment of Pathology and Cell Biology, Columbia University, New York City, New York. Electronic address: as4400@columbia.edu.
Columbia University · USUniversity of Pennsylvania · USUniversity of Pittsburgh · USShinshu University · JP

Funding

University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Weight loss-induced Microbiome and Adipokine Changes in Barrett's EsophagusU54CA163004 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ABRAMS, JULIAN, RUSTGI, ANIL K · 2011 to 2022
$12.5M
Novel Nanoscale Single-Cell Analysis of Exfoliative CytologyR01EB016657 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LIU, YANG · 2013 to 2016
$1.3M
(PQC2)Nanoscale changes in 3D nuclear architecture during breast tumorigenesisR01CA185363 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LIU, YANG · 2014 to 2017
$1.3M
NCATS NIH HHS UL1 TR000005NCATS NIH HHS UL1TR000005NCI NIH HHS 5U54CA163004NCI NIH HHS R01 CA185363NCI NIH HHS R01CA185363NCI NIH HHS U54 CA163004NIBIB NIH HHS R01 EB016657NIBIB NIH HHS R01EB016657
6 · The paper itself

Abstract

Barrett's intestinal metaplasia (BIM) may harbor genomic mutations before the histologic appearance of dysplasia and cancer and requires frequent surveillance. We explored next-generation sequencing to detect mutations with the analytical sensitivity required to predict concurrent high-grade dysplasia (HGD) and esophageal adenocarcinoma (EAC) in patients with Barrett's esophagus by testing nonneoplastic BIM. Formalin-fixed, paraffin-embedded (FFPE) routine biopsy or endoscopic mucosal resection samples from 32 patients were tested: nonprogressors to HGD or EAC (BIM-NP) with BIM, who never had a diagnosis of dysplasia or EAC (N = 13); progressors to HGD or EAC (BIM-P) with BIM and a worse diagnosis of HGD or EAC (N = 15); and four BIM-negative samples. No mutations were detected in the BIM-NP (0 of 13) or BIM-negative samples, whereas the BIM-P samples had mutations in 6 (75%) of 8 cases in TP53, APC, and CDKN2A (P = 0.0005), detected in samples with as low as 20% BIM. We found that next-generation sequencing from routine FFPE nonneoplastic Barrett's esophagus samples can detect multiple mutations in minute areas of BIM with high analytical sensitivity. Next-generation sequencing panels for detection of TP53 and possibly combined mutations in other genes, such as APC and CDKN2A, may be useful in the clinical setting to improve dysplasia and cancer surveillance in patients with Barrett's esophagus.

Indexed as

AdenocarcinomaAgedAged, 80 and overBarrett EsophagusBiomarkers, TumorEndoscopy, GastrointestinalEsophagusFemaleFormaldehydeHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMucous MembraneMutationParaffin EmbeddingBiomarkers, TumorFormaldehyde

Identifiers

PMID26068095
PMCPMC4484205
OpenAlexW1544917535

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.