Evidence map›Paper›PMID 26132737›Full record

ArticlePloS one2015

A Genetic Porcine Model of Cancer.

Lawrence B Schook, Tiago V Collares, Wenping Hu, Ying Liang, Fernanda M Rodrigues, Laurie A Rund, Kyle M Schachtschneider, Fabiana K Seixas, Kuldeep Singh, Kevin D Wells and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
13.7field-weighted citation impact, top 1% 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

105 citing papers in PubMed, 158 citations in OpenAlex.

  1. Article
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  9. Article
  10. Irreversible electroporation for treatment of colorectal cancer in a porcine model.VideoGIE : an official video journal of the American Society for Gastrointestinal Endoscopy · 2025
    Article
  11. Selective epithelial expression of KRASScientific reports · 2025
    Article
  12. Article
  13. Article
  14. Analysis of growth rate, haematologic, and biochemical parameters of Oncopigs.International journal of veterinary science and medicine · 2025
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

45 more citing papers are in PubMed but not listed here.

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 6 institutions in 3 countries.

Lawrence B SchookDepartment of Animal Sciences, University of Illinois, Champaign-Urbana, Illinois, United States of America; Department of Bioengineering, University of Illinois, Champaign-Urbana, Illinois, United States of America; Department of Surgery, University of Illinois, Chicago, Illinois, United States of America.
Tiago V CollaresTechnology Development Center, Postgraduate Program in Biotechnology, Federal University of Pelotas, Pelotas, Rio Grande do Sul, Brazil.
Wenping HuState Key Laboratory of AgroBiotechnology, China Agricultural University, Beijing, China.
Ying LiangDepartment of Internal Medicine, University of Kentucky, Lexington, Kentucky, United States of America.
Fernanda M RodriguesDepartment of Animal Sciences, University of Illinois, Champaign-Urbana, Illinois, United States of America.
Laurie A RundDepartment of Animal Sciences, University of Illinois, Champaign-Urbana, Illinois, United States of America.
Kyle M SchachtschneiderDepartment of Animal Sciences, University of Illinois, Champaign-Urbana, Illinois, United States of America.
Fabiana K SeixasTechnology Development Center, Postgraduate Program in Biotechnology, Federal University of Pelotas, Pelotas, Rio Grande do Sul, Brazil.
Kuldeep SinghVeterinary Diagnostic Laboratory, University of Illinois, Champaign-Urbana, Illinois, United States of America.
Kevin D WellsDivision of Animal Science, National Swine Research and Resource Center, University of Missouri, Columbia, Missouri, United States of America.
Eric M WaltersDivision of Animal Science, National Swine Research and Resource Center, University of Missouri, Columbia, Missouri, United States of America.
Randall S PratherDivision of Animal Science, National Swine Research and Resource Center, University of Missouri, Columbia, Missouri, United States of America.
Christopher M CounterDepartment of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, North Carolina, United States of America; Department of Radiation Oncology, Duke University Medical Center, Durham, North Carolina, United States of America.
University of Illinois Urbana-Champaign · USUniversity of Missouri · USUniversidade Federal de Pelotas · BRChina Agricultural University · CNDuke Medical Center · USUniversity of Kentucky · US

Funding

Resource Core for National Swine Resource and Research Center (NSRRC) Years 21-25U42OD011140 · OD · UNIVERSITY OF MISSOURI-COLUMBIA · PI Kiho Lee, Kevin Dale Wells · 2012 to 2026
$26.7M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
Dynamic requirements of Ras signaling during cancerR01CA123031 · NCI · DUKE UNIVERSITY · PI COUNTER, CHRISTOPHER M · 2007 to 2018
$3.5M
Kentucky Center for Clinical and Translational ScienceKL2TR000116 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$1.9M
Oncopigs as a better model for human cancerR01CA153132 · NCI · UNIVERSITY OF LOUISVILLE · PI CLARK, GEOFFREY J., RUND, LAURETTA · 2010 to 2013
$1.0M
NCATS NIH HHS KL2 TR000116NCATS NIH HHS UL1 TR000117NCI NIH HHS CA123031NCI NIH HHS CA 153132NCI NIH HHS R01 CA123031NCI NIH HHS R01 CA153132NIH HHS U42 OD011140
6 · The paper itself

Abstract

The large size of the pig and its similarity in anatomy, physiology, metabolism, and genetics to humans make it an ideal platform to develop a genetically defined, large animal model of cancer. To this end, we created a transgenic "oncopig" line encoding Cre recombinase inducible porcine transgenes encoding KRASG12D and TP53R167H, which represent a commonly mutated oncogene and tumor suppressor in human cancers, respectively. Treatment of cells derived from these oncopigs with the adenovirus encoding Cre (AdCre) led to KRASG12D and TP53R167H expression, which rendered the cells transformed in culture and tumorigenic when engrafted into immunocompromised mice. Finally, injection of AdCre directly into these oncopigs led to the rapid and reproducible tumor development of mesenchymal origin. Transgenic animals receiving AdGFP (green fluorescent protein) did not have any tumor mass formation or altered histopathology. This oncopig line could thus serve as a genetically malleable model for potentially a wide spectrum of cancers, while controlling for temporal or spatial genesis, which should prove invaluable to studies previously hampered by the lack of a large animal model of cancer.

Indexed as

Genetic Predisposition to DiseaseAnimalsAnimals, Genetically ModifiedCell Transformation, NeoplasticDisease Models, AnimalFemaleFibroblastsGene ExpressionGene OrderGenes, p53Genes, rasGenes, ReporterGene TargetingHeterograftsMaleMice

Identifiers

PMID26132737
PMCPMC4488487
OpenAlexW1577149770

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.