Evidence map›Paper›PMID 33029223›Full record

ReviewAnimal reproduction2020

A decade of experience with genetically tailored pig models for diabetes and metabolic research.

Silja Zettler, Simone Renner, Elisabeth Kemter, Arne Hinrichs, Nikolai Klymiuk, Mattias Backman, Evamaria Olga Riedel, Christiane Mueller, Elisabeth Streckel, Christina Braun-Reichhart and 11 more

Abstract readReview
In one paragraph

Review in Animal reproduction, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  5. Article
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  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Pig Models in Retinal Research and Retinal Disease.Cold Spring Harbor perspectives in medicine · 2024
    Review
  13. Review
  14. An inducible model of chronic hyperglycemia.Disease models & mechanisms · 2023
    Article
  15. Article
  16. Review
  17. 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

21 authors.

Silja ZettlerMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0003-0171-012X
Simone RennerMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0002-5866-4577
Elisabeth KemterMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0001-7785-7502
Arne HinrichsMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0003-3022-5983
Nikolai KlymiukMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0003-3532-1659
Mattias BackmanLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich.ORCID 0000-0001-5753-8045
Evamaria Olga RiedelLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich.ORCID 0000-0003-2259-9221
Christiane MuellerMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0003-3686-5770
Elisabeth StreckelMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0002-2562-0092
Christina Braun-ReichhartMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0001-7582-6884
Ana Sofia MartinsMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0001-9514-766X
Mayuko KuromeMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0002-2725-8613
Barbara KeßlerMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0001-7036-238X
Valeri ZakhartchenkoMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0002-5974-9759
Florian FlenkenthalerLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich.ORCID 0000-0003-2964-9236
Georg Josef ArnoldLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich.ORCID 0000-0002-2716-0229
Thomas FröhlichLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich.ORCID 0000-0002-4709-3211
Helmut BlumLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich.ORCID 0000-0002-3994-2332
Andreas BlutkeResearch Unit Analytical Pathology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.ORCID 0000-0001-7824-2681
Rüdiger WankeInstitute of Veterinary Pathology, Center for Clinical Veterinary Medicine, LMU Munich, Munich, Germany.ORCID 0000-0002-0153-224X
Eckhard WolfMolecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.ORCID 0000-0002-0430-9510

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global prevalence of diabetes mellitus and other metabolic diseases is rapidly increasing. Animal models play pivotal roles in unravelling disease mechanisms and developing and testing therapeutic strategies. Rodents are the most widely used animal models but may have limitations in their resemblance to human disease mechanisms and phenotypes. Findings in rodent models are consequently often difficult to extrapolate to human clinical trials. To overcome this 'translational gap', we and other groups are developing porcine disease models. Pigs share many anatomical and physiological traits with humans and thus hold great promise as translational animal models. Importantly, the toolbox for genetic engineering of pigs is rapidly expanding. Human disease mechanisms and targets can therefore be reproduced in pigs on a molecular level, resulting in precise and predictive porcine (PPP) models. In this short review, we summarize our work on the development of genetically (pre)diabetic pig models and how they have been used to study disease mechanisms and test therapeutic strategies. This includes the generation of reporter pigs for studying beta-cell maturation and physiology. Furthermore, genetically engineered pigs are promising donors of pancreatic islets for xenotransplantation. In summary, genetically tailored pig models have become an important link in the chain of translational diabetes and metabolic research.

Indexed as

biobankdiabetespig modelxenotransplantation

Identifiers

PMID33029223
PMCPMC7534555

What OpenQuestion holds

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LicenceCC BY
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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.