Evidence map›Paper›PMID 41899420›Full record

ArticleCurrent issues in molecular biology2026

E-Cadherin Is an Accurate Target for Fluorescence-Guided Imaging of Lymph Nodes.

Kelly A McGovern, Katherine O Welch, Jake Mlakar, Ryan Krouse, Michael Brown, Lydia Chen, Kevin Guo, Jeffrey Huang, Edward J Delikatny, Viktor Gruev and 2 more

Abstract read
In one paragraph

Article in Current issues in molecular biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Kelly A McGovernDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Katherine O WelchDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Jake MlakarDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0009-0003-7950-8930
Ryan KrouseDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0009-0006-8350-1717
Michael BrownDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Lydia ChenDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Kevin GuoDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0009-0008-6989-5611
Jeffrey HuangDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Edward J DelikatnyDepartment of Radiology, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Viktor GruevDepartment of Engineering and Computer Engineering, University of Illinois at Urbana-Champaign, 306 N Wright St, Urbana, IL 61801, USA.
Paul ZhangDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Sunil SinghalDepartment of Thoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-2413-7082

Funding

Shared Resource - Core A: Administrative CoreP01CA254859 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Madduri S Srinivasarao · 2022 to 2026
$10.0M
SURGICAL ONCOLOGY RESEARCH TRAINING PROGRAM AT PENNT32CA251063 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Ronald P. Dematteo · 2020 to 2026
$2.6M
NCI NIH HHS P01 CA254859NCI NIH HHS T32 CA251063NIH Common Fund T32 CA251063-05
6 · The paper itself

Abstract

Lymph node (LN) dissection is a necessary part of every oncologic surgery in order to provide important information for staging, predicting prognosis and improving survival. To do this, surgical oncologists strive to localize and dissect every pathologically positive LN while avoiding the increased morbidity of removing true negative LNs. The goal is to develop an imaging method to distinguish positive and negative LNs, but a specific biomarker is missing. Thus, our aim is to identify a reliable imaging marker for identifying LNs with lung cancer cells. After screening many epithelial markers, we identified E-cadherin, a membrane protein normally expressed in epithelial cells, including in the lung. To follow up on our potential target, we performed immunofluorescence staining on 48 human LNs with a conjugated anti-E-cadherin monoclonal antibody. Fluorescence was significantly higher in LNs with metastasis, as shown in 48 positive LNs from patients with resected primary lung cancer. There was high fluorescence in both hilar and mediastinal LNs, and in all primary tumor histologies. E-cadherin may be useful for the surgical oncologist for targeted imaging technologies for selecting positive LNs from lung cancer.

Indexed as

biomarkerfluorescence-guided imagingintraoperative molecular imaginglung cancer

Identifiers

PMID41899420
PMCPMC13025594

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