Evidence map›Paper›PMID 27305144›Full record

ArticleOncology2016

Validation of a Preclinical Model of Diethylnitrosamine-Induced Hepatic Neoplasia in Yucatan Miniature Pigs.

Jennifer Mitchell, Peggy T Tinkey, Rony Avritscher, Carolyn Van Pelt, Ghazaleh Eskandari, Suraj Konnath George, Lianchun Xiao, Erik Cressman, Jeffrey S Morris, Asif Rashid and 3 more

Open access · hybridAbstract readValidation Study
In one paragraph

Article in Oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Effect of CRISPR Knockout ofFrontiers in oncology · 2022
    Article
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  8. 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 4 institutions in 2 countries.

Jennifer MitchellDepartment of Veterinary Medicine and Surgery, The University of Texas MD Anderson Cancer Center, Houston, Tex., USA.
Peggy T Tinkey
Rony Avritscher
Carolyn Van Pelt
Ghazaleh Eskandari
Suraj Konnath George
Lianchun Xiao
Erik Cressman
Jeffrey S Morris
Asif Rashid
Ahmed O Kaseb
Hesham M Amin
Rajesh Uthamanthil
University of Veterinary Medicine · HUCancer Research And Biostatistics · USDayton Interventional Radiology · USThe University of Texas MD Anderson Cancer Center · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Role of IGF-IR tyrosine kinase in NPM-ALK-expressing T-cell lymphomaR01CA151533 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AMIN, HESHAM M · 2011 to 2015
$1.6M
NCI NIH HHS P30 CA015704NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA151533
6 · The paper itself

Abstract

objectiveThe purpose of this study was to reduce the time to tumor onset in a diethylnitrosamine (DEN)-induced hepatocellular carcinoma (HCC) swine model via partial liver embolization (PLE) and to characterize the model for use in translational research.

methodsEight Yucatan miniature pigs were injected intraperitoneally with either saline (n = 2) or DEN (n = 6) solution weekly for 12 weeks. Three of the DEN-treated pigs underwent PLE. The animals underwent periodic radiological evaluation, liver biopsy, and blood sampling, and full necropsy was performed at study termination (∼29 months).

resultsAll DEN-treated pigs developed hepatic adenoma and HCC. PLE accelerated the time to adenoma development but not to HCC development. Biomarker analysis results showed that IGF1 levels decreased in all DEN-treated pigs as functional liver capacity decreased with progression of HCC. VEGF and IL-6 levels were positively correlated with disease progression. Immunohistochemical probing of HCC tissues demonstrated the expression of several important survival-promoting proteins.

conclusionTo our knowledge, we are the first to demonstrate an accelerated development of hepatic neoplasia in Yucatan miniature pigs. Our HCC swine model closely mimics the human condition (i.e., progressive disease stages and expression of relevant molecular markers) and is a viable translational model.

Indexed as

Disease Models, AnimalAdenomaalpha-FetoproteinsAnimalsCarcinoma, HepatocellularDiethylnitrosamineEmbolismFemaleGrowth HormoneInsulin-Like Growth Factor IInterleukin-6Janus Kinase 2Liver Neoplasms, ExperimentalPortal VeinReceptors, SomatomedinSTAT3 Transcription Factoralpha-FetoproteinsDiethylnitrosamineGrowth HormoneInsulin-Like Growth Factor IInterleukin-6Janus Kinase 2Receptors, SomatomedinSTAT3 Transcription FactorSTAT5 Transcription FactorVascular Endothelial Growth Factor A

Identifiers

PMID27305144
PMCPMC5432216
OpenAlexW2428513127

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

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.