Evidence map›Paper›PMID 35006394›Full record

ArticleEJNMMI research2022

CXCR4 peptide-based fluorescence endoscopy in a mouse model of Barrett's esophagus.

Sabrina Marcazzan, Marcos J Braz Carvalho, Matthias Konrad, Julia Strangmann, Anna Tenditnaya, Theresa Baumeister, Roland M Schmid, Hans-Jürgen Wester, Vasilis Ntziachristos, Dimitris Gorpas and 3 more

Open access · goldAbstract read
In one paragraph

Article in EJNMMI research, 2022. 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
5.0field-weighted citation impact, top 4% 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, 24 citations in OpenAlex.

  1. Review
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  4. Targeting c-MET for Endoscopic Detection of Dysplastic Lesions within Barrett's Esophagus Using EMI-137 Fluorescence Imaging.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
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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

13 authors at 8 institutions in 4 countries.

Sabrina MarcazzanII Medizinische Klinik, Klinikum rechts der isar, Technische Universität München, Munich, Germany.
Marcos J Braz CarvalhoII Medizinische Klinik, Klinikum rechts der isar, Technische Universität München, Munich, Germany.
Matthias KonradInstitut für Pharmazeutische Radiochemie, Technische Universität München, Munich, Germany.
Julia StrangmannII Medizinische Klinik, Klinikum rechts der isar, Technische Universität München, Munich, Germany.
Anna TenditnayaChair of Biological Imaging, School of Medicine, Technische Universität München, Munich, Germany.
Theresa BaumeisterII Medizinische Klinik, Klinikum rechts der isar, Technische Universität München, Munich, Germany.
Roland M SchmidII Medizinische Klinik, Klinikum rechts der isar, Technische Universität München, Munich, Germany.
Hans-Jürgen WesterInstitut für Pharmazeutische Radiochemie, Technische Universität München, Munich, Germany.
Vasilis NtziachristosChair of Biological Imaging, School of Medicine, Technische Universität München, Munich, Germany.
Dimitris GorpasChair of Biological Imaging, School of Medicine, Technische Universität München, Munich, Germany.
Timothy C WangDivision of Digestive and Liver Diseases, Columbia University Irving Medical Center, New York, NY, USA.
Margret SchotteliusInstitut für Pharmazeutische Radiochemie, Technische Universität München, Munich, Germany.
Michael QuanteII Medizinische Klinik, Klinikum rechts der isar, Technische Universität München, Munich, Germany. michael.quante@uniklinik-freiburg.de.ORCID http://orcid.org/0000-0002-8497-582X
Helmholtz Zentrum München · DETUM Klinikum · DETechnical University of Munich · DEColumbia University Irving Medical Center · USInnsbruck Medical University · ATUniversity Hospital of Lausanne · CHUniversity Medical Center Freiburg · DEUniversity of Freiburg · DE

Funding

Deutsche Forschungsgemeinschaft SFB 84: B05
6 · The paper itself

Abstract

backgroundNear-infrared (NIR) fluorescence imaging has been emerging as a promising strategy to overcome the high number of early esophageal adenocarcinomas missed by white light endoscopy and random biopsy collection. We performed a preclinical assessment of fluorescence imaging and endoscopy using a novel CXCR4-targeted fluorescent peptide ligand in the L2-IL1B mouse model of Barrett's esophagus.

methodsSix L2-IL1B mice with advanced stage of disease (12-16 months old) were injected with the CXCR4-targeted, Sulfo-Cy5-labeled peptide (MK007), and ex vivo wide-field imaging of the whole stomach was performed 4 h after injection. Before ex vivo imaging, fluorescence endoscopy was performed in three L2-IL1B mice (12-14 months old)  by a novel imaging system with two L2-IL1B mice used as negative controls.

resultsEx vivo imaging and endoscopy in L2-IL1B mice showed that the CXCR4-targeted MK007 accumulated mostly in the dysplastic lesions with a mean target-to-background ratio > 2. The detection of the Sulfo-Cy5 signal in dysplastic lesions and its co-localization with CXCR4 stained cells  by confocal microscopy further confirmed the imaging results.

conclusionsThis preliminary preclinical study shows that CXCR4-targeted fluorescence endoscopy using MK007 can detect dysplastic lesions in a mouse model of Barrett's esophagus. Further investigations are needed to assess its use in the clinical setting.

Indexed as

Animal modelsBarrett’s esophagusCXCR4DysplasiaEndoscopyEsophageal cancerFluorescence imagingMolecular imagingPeptide

Identifiers

PMID35006394
PMCPMC8748556
OpenAlexW4206824236

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.