Evidence map›Paper›PMID 28430953›Full record

ArticleAmerican journal of clinical pathology2016

Gastric Proteins MUC5AC and TFF1 as Potential Diagnostic Markers of Colonic Sessile Serrated Adenomas/Polyps.

Magomed Khaidakov, Keith K Lai, D Roudachevski, Julietta Sargsyan, Hannah E Goyne, Rish K Pai, Laura W Lamps, Curt H Hagedorn

Open access · hybridAbstract read
In one paragraph

Article in American journal of clinical pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Specific Targeting and Labeling of Colonic Polyps inCurrent issues in molecular biology · 2023
    Article
  11. Article
  12. Cell plasticity in regeneration in the stomach and beyond.Current opinion in genetics & development · 2022
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. The role of CDX2, MUC5AC, and p53 in the evaluation of the progression of serrated lesions toward colorectal carcinoma.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
  19. 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

8 authors at 3 institutions in 1 country.

Magomed KhaidakovFrom the Department of Medicine.
Keith K LaiDepartment of Pathology, University of Arkansas for Medical Sciences, Little Rock.
D RoudachevskiCentral Arkansas Veterans Healthcare System, Little Rock.
Julietta SargsyanCentral Arkansas Veterans Healthcare System, Little Rock.
Hannah E GoyneDepartment of Pathology, University of Arkansas for Medical Sciences, Little Rock.
Rish K PaiDepartment of Pathology, Mayo Clinic, Scottsdale, AZ.
Laura W LampsDepartment of Pathology, University of Arkansas for Medical Sciences, Little Rock.
Curt H HagedornFrom the Department of Medicine.
Central Arkansas Veterans Healthcare System · USUniversity of Arkansas for Medical Sciences · USMayo Clinic in Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesA subset of colon cancers originates from sessile serrated adenomas/polyps (SSA/Ps). Our goal was to identify markers for SSA/Ps that could aid in distinguishing them from hyperplastic polyps (HPs).

methodsWe performed immunostaining for gastric proteins MUC5AC and TFF1 in formalin-fixed, paraffin-embedded (FFPE) samples of HPs (n = 47), SSA/Ps (n = 37), and normal colon (n = 30).

resultsControl mucosa expressed only trace amounts of MUC5AC and TFF1. HPs exhibited an 11.3- and 11.4-fold increase in MUC5AC and TFF1 expression confined to the upper segments of the crypts near the luminal surface of the polyps. SSA/Ps displayed on average 1.6-fold (MUC5AC, P  < .008) and 1.4-fold (TFF1, P  < .03) higher signal intensity for these markers than HPs, with a dramatic coexpression of MUC5AC and TFF1 typically occupying the entire length of the crypt. Immunoperoxidase results were similar to immunofluorescence staining for both MUC5AC and TFF1.

conclusionsOur results suggest that the analysis of expression of MUC5AC and TFF1 may be useful for differentiating SSA/Ps from HPs. We also suggest the possibility that crypt morphology may be at least partly due to overproduction of highly viscous gastric mucins and that these proteins may play a role in the serrated pathway to colon carcinogenesis.

Indexed as

AdenomaBiomarkers, TumorColonColonic NeoplasmsColonic PolypsDiagnosis, DifferentialHumansHyperplasiaImmunohistochemistryMucin 5ACTrefoil Factor-1Biomarkers, TumorMUC5AC protein, humanMucin 5ACTFF1 protein, humanTrefoil Factor-1Colon cancerHyperplastic polypsMUC5ACSerrated polypsSessile serrated adenomas/polypsTFF1

Identifiers

PMID28430953
PMCPMC5377921
OpenAlexW2536729445

What OpenQuestion holds

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Registered trials

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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.