Evidence map›Paper›PMID 41498244›Full record

ArticleAnimal models and experimental medicine2026

Characterization of inflammatory pseudotumors in a large animal model of liver cancer.

Erik N K Cressman, Samantha Hicks, Natalie W Fowlkes, Danielle L Stolley, Maria Sophia Stenkamp

Abstract read
In one paragraph

Article in Animal models and experimental medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Undifferentiated carcinomas in a large animal model of liver cancer.Animal models and experimental medicine · 2026
    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

5 authors.

Erik N K CressmanDepartment of Interventional Radiology, MD Anderson Cancer Center, The University of Texas, Houston, Texas, USA.ORCID 0000-0002-8671-9862
Samantha HicksDepartment of Veterinary Medicine and Surgery, MD Anderson Cancer Center, The University of Texas, Houston, Texas, USA.
Natalie W FowlkesDepartment of Veterinary Medicine and Surgery, MD Anderson Cancer Center, The University of Texas, Houston, Texas, USA.
Danielle L StolleyFlow Cytometry & Cellular Imaging Core Facility, MD Anderson Cancer Center, The University of Texas, Houston, Texas, USA.
Maria Sophia StenkampDepartment of Veterinary Medicine and Surgery, MD Anderson Cancer Center, The University of Texas, Houston, Texas, USA.

Funding

UPWARDS Training Program (Underrepresented Minorities Working Towards Research Diversity in Science)R25CA240137 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KEYOMARSI, KHANDAN, WATOWICH, STEPHANIE S · 2020 to 2024
$2.1M
Institutional Research Grant, MD Anderson Cancer CenterNCI NIH HHS R25 CA240137the CPRIT Research Training Award CPRIT Training Program RP210028UPWARDS Training Program (Undergraduate Students Working Towards Research in Science) 1R25CA240137-01A1
6 · The paper itself

Abstract

backgroundThe development of relevant and robust large animal models of hepatocellular carcinoma is needed to test new therapeutic strategies for this disease. Transgenic approaches hold promise in addressing this complex problem. One such model, the Oncopig, has been reported to develop tumors of up to 4 cm in diameter within 7-14 days at sites of in situ vector inoculation. However, the resulting lesions reportedly contained an extensive inflammatory component that has not been evaluated in detail.

methodsHerein, we describe our results from multiparametric characterization of the lesions generated using liver biopsy cores incubated in vector solution and replaced in the tissue. The study consisted of 3 animals in 3 cohorts (total of 9 animals) that were evaluated at 14, 21, and 28 days. CT imaging, immunohistochemistry, multiplex immunofluorescence, and comprehensive blood analyses were used to quantify composition of the hepatic masses that developed following AdCre inoculation.

resultsThe tumors were hypovascular on CT and predominantly composed of CD45+ cells with a strong lymphohistiocytic component, with no carcinomas identified. Ki-67 staining showed proliferation of CD45+ immune cells but no neoplastic component. To provide further insight, the results are evaluated in the context of tumor growth kinetics.

conclusionWhile progress has been made in generating targetable lesions, achieving a robust large animal model of liver cancer that faithfully recapitulates the human disease remains a challenging goal.

Indexed as

Carcinoma, HepatocellularDisease Models, AnimalGranuloma, Plasma CellLiver NeoplasmsLiver Neoplasms, ExperimentalAnimalsFemaleLiverTomography, X-Ray Computedanimals, genetically modifieddisease models, animalsolid tumorsswine

Identifiers

PMID41498244
PMCPMC13042422

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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.