Evidence map›Paper›PMID 31990272›Full record

RevieweLife2020

Preclinical murine tumor models: a structural and functional perspective.

Marion V Guerin, Veronica Finisguerra, Benoit J Van den Eynde, Nadege Bercovici, Alain Trautmann

Abstract readReview
In one paragraph

Review in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed, 4 pooled it
–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

98 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Article
  7. New developments and applications of human organoids.Nature reviews. Molecular cell biology · 2026
    Review
  8. Article
  9. Article
  10. Review
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  12. How Key in vivo Models Can Advance Anticancer Nanotherapeutics.International journal of nanomedicine · 2026
    Review
  13. Article
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  18. Peptide vaccine formulations with structurally distinct STING agonist drugamers induce discrete, efficacious antitumor responses.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  19. Review
  20. Article

38 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

5 authors.

Marion V GuerinUniversité de Paris, Institut Cochin, INSERM, U1016, CNRS, UMR8104, F-75014, Paris, France.ORCID https://orcid.org/0000-0003-2159-8518
Veronica FinisguerraLudwig Institute for Cancer Research, de Duve Institute WELBIO, UCLouvain, Brussels, Belgium.ORCID http://orcid.org/0000-0002-2455-9939
Benoit J Van den EyndeLudwig Institute for Cancer Research, de Duve Institute WELBIO, UCLouvain, Brussels, Belgium.ORCID https://orcid.org/0000-0002-4995-3270
Nadege BercoviciUniversité de Paris, Institut Cochin, INSERM, U1016, CNRS, UMR8104, F-75014, Paris, France.ORCID http://orcid.org/0000-0002-8449-0590
Alain TrautmannUniversité de Paris, Institut Cochin, INSERM, U1016, CNRS, UMR8104, F-75014, Paris, France.ORCID https://orcid.org/0000-0001-7514-420X

Funding

Centre National de la Recherche Scientifique Core fundingFonds De La Recherche Scientifique - FNRS 28095636Inserm Core fundingLigue Contre le Cancer RS18/75-61Ministère de l'Éducation Nationale Graduate Student FellowshipParis Descartes University Core fundingWorldwide Cancer Research AICR # 13-0260
6 · The paper itself

Abstract

The goal of this review is to pinpoint the specific features, including the weaknesses, of various tumor models, and to discuss the reasons why treatments that are efficient in murine tumor models often do not work in clinics. In a detailed comparison of transplanted and spontaneous tumor models, we focus on structure-function relationships in the tumor microenvironment. For instance, the architecture of the vascular tree, which depends on whether tumor cells have gone through epithelial-mesenchymal transition, is determinant for the extension of the spontaneous necrosis, and for the intratumoral localization of the immune infiltrate. Another key point is the model-dependent abundance of TGFβ in the tumor, which controls the variable susceptibility of different tumor models to treatments. Grounded in a historical perspective, this review provides a rationale for checking factors that will be key for the transition between preclinical murine models and clinical applications.

Indexed as

Disease Models, AnimalAnimalsCarcinogensMiceNeoplasm MetastasisNeoplasmsNeoplasm TransplantationOrgan SpecificityCarcinogenscancer biologyEMTimmunologyinflammationmicroenvironmentspontaneous tumorsTGFβtransplanted tumorsvascularization

Identifiers

PMID31990272
PMCPMC6986875

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.