Evidence map›Paper›PMID 33669017›Full record

ReviewCancers2021

Mouse Models of Peritoneal Carcinomatosis to Develop Clinical Applications.

Ángela Bella, Claudia Augusta Di Trani, Myriam Fernández-Sendin, Leire Arrizabalaga, Assunta Cirella, Álvaro Teijeira, José Medina-Echeverz, Ignacio Melero, Pedro Berraondo, Fernando Aranda

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. [Efficacy of CD4/TGF-β bispecific antibody in a mouse model of peritoneal metastasis of malignant melanoma].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
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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

10 authors at 2 institutions in 2 countries.

Ángela BellaProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0002-6534-7705
Claudia Augusta Di TraniProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0002-7423-2352
Myriam Fernández-SendinProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0003-2119-3967
Leire ArrizabalagaProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.
Assunta CirellaProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.
Álvaro TeijeiraProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0002-7339-4464
José Medina-EcheverzBavarian Nordic GmbH, Fraunhoferstrasse 13, 82152 Planegg, Germany.
Ignacio MeleroProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0002-1360-348X
Pedro BerraondoProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0001-7410-1865
Fernando ArandaProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0002-9364-474X
Navarre Institute of Health Research · ESBavarian Nordic (Germany) · DE

Funding

Horizon 2020 Framework Programme No 765394Instituto de Salud Carlos III CP19/00114Instituto de Salud Carlos III FI20/00058Instituto de Salud Carlos III PI19/01128Instituto de Salud Carlos III PI20/00002La Caixa research 269 foundation LCF/BQ/LR18/11640014TRANSCAN456 2 TRS-2016-00000371
6 · The paper itself

Abstract

Peritoneal carcinomatosis of primary tumors originating in gastrointestinal (e.g., colorectal cancer, gastric cancer) or gynecologic (e.g., ovarian cancer) malignancies is a widespread type of tumor dissemination in the peritoneal cavity for which few therapeutic options are available. Therefore, reliable preclinical models are crucial for research and development of efficacious treatments for this condition. To date, a number of animal models have attempted to reproduce as accurately as possible the complexity of the tumor microenvironment of human peritoneal carcinomatosis. These include: Syngeneic tumor cell lines, human xenografts, patient-derived xenografts, genetically induced tumors, and 3D scaffold biomimetics. Each experimental model has its own strengths and limitations, all of which can influence the subsequent translational results concerning anticancer and immunomodulatory drugs under exploration. This review highlights the current status of peritoneal carcinomatosis mouse models for preclinical development of anticancer drugs or immunotherapeutic agents.

Indexed as

animal modelmetastasisperitoneal carcinomatosisperitoneal microenvironmenttranslational research

Identifiers

PMID33669017
PMCPMC7956655
OpenAlexW3129755462

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.