Evidence map›Paper›PMID 41792707›Full record

ArticleBMC oral health2026

Open-field fluorescence guided imaging of ameloblastoma tumors in mouse patient-derived xenograft model.

Hope M Amm, Beta C Idigo, Logan D Stone, Revati Suryawanshi, Sherin James, Nisha J D'Silva, Eben L Rosenthal, Anthony B Morlandt

Abstract read
In one paragraph

Article in BMC oral health, 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

8 authors.

Hope M Amm *Department of Oral and Maxillofacial Surgery, University of Alabama at Birmingham, 1919 7th Ave S, SDB 419, Birmingham, AL, 35294, USA. hopeamm@uab.edu.ORCID 0000-0003-2416-9575
Beta C Idigo *Department of Oral and Maxillofacial Surgery, University of Alabama at Birmingham, 1919 7th Ave S, SDB 419, Birmingham, AL, 35294, USA.
Logan D Stone *Department of Oral and Maxillofacial Surgery, University of Alabama at Birmingham, 1919 7th Ave S, SDB 419, Birmingham, AL, 35294, USA.
Revati SuryawanshiDepartment of Oral and Maxillofacial Surgery, University of Alabama at Birmingham, 1919 7th Ave S, SDB 419, Birmingham, AL, 35294, USA.
Sherin JamesDepartment of Otolaryngology, University of Alabama at Birmingham, 1670 University Blvd, VH G082, Birmingham, AL, 35294, USA.
Nisha J D'SilvaDepartment of Periodontics and Oral Medicine, University of Michigan, 1011 N. University, Room 5216, Ann Arbor, MI, 48109, USA.
Eben L RosenthalDepartment of Otolaryngology, Vanderbilt University Medical Center, 1500 E Medical Center Drive, Nashville, TN, 37212, USA.
Anthony B MorlandtDepartment of Oral and Maxillofacial Surgery, University of Alabama at Birmingham, 1919 7th Ave S, SDB 419, Birmingham, AL, 35294, USA. amorlandt@uabmc.edu.

Funding

NIDCR NIH HHS K99/R00-DE023826NIDCR NIH HHS T90-DE022736Oral and Maxillofacial Surgery Foundation Research Support Grant 2015
6 · The paper itself

Abstract

purposeThe aim of our study is to use near infrared fluorescence imaging to demonstrate the localization of cetuximab-IRDye800 to ameloblastoma in vivo.

methodsAmeloblastoma tumor tissue from three patients was implanted subcutaneously into athymic nude mice to form patient-derived xenografts (PDX). Animals were randomly divided into two groups; one received the epidermal growth factor receptor (EGFR) antibody, cetuximab-IRDye800, and the other received the control antibody, IgG-IRDye800. After resection of the overlying skin, the tumors were imaged on the LUNA device, an open-field, intraoperative device. Tumor/background ratios (TBRs) were calculated and statistically analyzed using a paired t test.

resultsImaging of PDX tumors revealed the TBRs produced by cetuximab-IRDye800 (AB-20, 4.5 ± 1.57; AB-33, 1.17 ± 0.42; AB-34, 1.33 ± 0.04) were significantly higher than those produced by IgG-IRDye800 (AB-20, 2.02 ± 0.29; AB-33, 1.07 ± 0.30; AB-34, 1.11 ± 0.13; p values, AB-20, p < 0.021; AB-33; p < 0.045; AB-34; p < 0.017). Excised PDX tissues were paraffin-embedded to confirm the presence of tumor by H&E staining and EGFR expression.

conclusionFluorescently labeled anti-EGFR demonstrates specificity and sensitivity for PDX tumor xenografts using an open-field, near-infrared imaging system. These open-field devices allow real-time clinical assessment of fluorescent signals during surgery and may provide future benefit in the removal of ameloblastoma tumors.

Indexed as

AmeloblastomaOptical ImagingAnimalsCetuximabErbB ReceptorsFemaleHeterograftsHumansMiceMice, NudeCetuximabErbB ReceptorsAmeloblastomaEGFR protein, humanOdontogenic TumorsOptical imaging

Identifiers

PMID41792707
PMCPMC13077876

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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.