Evidence map›Paper›PMID 22245781›Full record

ArticleNature medicine2012

Molecular imaging using fluorescent lectins permits rapid endoscopic identification of dysplasia in Barrett's esophagus.

Elizabeth L Bird-Lieberman, André A Neves, Pierre Lao-Sirieix, Maria O'Donovan, Marco Novelli, Laurence B Lovat, William S Eng, Lara K Mahal, Kevin M Brindle, Rebecca C Fitzgerald

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04161560 (Cetuximab - IRDye800 Intraoperative Fluorescence Imaging in Esophagectomy of Esophageal Cancer), which is not on this map. Cited by 115 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed, 1 pooled it
14.9field-weighted citation impact, top 1% 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.

NCT04161560 phase1unknown statusnot on this mapstarted 2019, after this paper: background citation

Cetuximab - IRDye800 Intraoperative Fluorescence Imaging in Esophagectomy of Esophageal Cancer:A Single Center Clinical Research

TypeinterventionalSponsorFifth Affiliated Hospital, Sun Yat-Sen UniversityRan2019 to 2021Enrolled40ConditionsDrug Safety, Drug SpecificityArmsCetuximab-IRDye800
3 · Its place in the literature

Who cites it

115 citing papers in PubMed, 1 synthesis or guideline pooled it, 235 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Translational cancer research · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Targeted Hsp70 fluorescence molecular endoscopy detects dysplasia in Barrett's esophagus.European journal of nuclear medicine and molecular imaging · 2022
    Article
  13. 360Photoacoustics · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

55 more citing papers are in PubMed but not listed here.

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

10 authors at 6 institutions in 2 countries.

Elizabeth L Bird-LiebermanMedical Research Council Cancer Cell Unit, Hutchison/MRC Research Centre, Cambridge, UK.
André A Neves
Pierre Lao-Sirieix
Maria O'Donovan
Marco Novelli
Laurence B Lovat
William S Eng
Lara K Mahal
Kevin M Brindle
Rebecca C Fitzgerald
Medical Research Council · GBNew York University · USUniversity College London · GBUniversity of Cambridge · GBAddenbrooke's Hospital · GBHutchison/MRC Research Centre · GB

Funding

Cancer Research UKDepartment of HealthMedical Research Council MC_U105365007
6 · The paper itself

Abstract

Barrett's esophagus is an example of a pre-invasive state, for which current endoscopic surveillance methods to detect dysplasia are time consuming and inadequate. The prognosis of cancer arising in Barrett's esophagus is improved by early detection at the stage of mucosal carcinoma or high-grade dysplasia. Molecular imaging methods could revolutionize the detection of dysplasia, provided they permit a wide field of view and highlight abnormalities in real time. We show here that cell-surface glycans are altered in the progression from Barrett's esophagus to adenocarcinoma and lead to specific changes in lectin binding patterns. We chose wheat germ agglutinin as a candidate lectin with clinical potential. The binding of wheat germ agglutinin to human tissue was determined to be specific, and we validated this specific binding by successful endoscopic visualization of high-grade dysplastic lesions, which were not detectable by conventional endoscopy, with a high signal-to-background ratio of over 5.

Indexed as

Wheat Germ AgglutininsAgedAged, 80 and overBarrett EsophagusEsophageal NeoplasmsEsophagoscopyEsophagusFemaleFluorescenceGlycosphingolipidsHumansMaleMiddle AgedMolecular ImagingPrecancerous ConditionsGlycosphingolipidsWheat Germ Agglutinins

Identifiers

PMID22245781
OpenAlexW1980863117

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.