Evidence map›Paper›PMID 41285854›Full record

ArticleNature communications2025

Immunological surveillance against cancer across mammals.

Orsolya Vincze, Piotr Minias, Alexandre Corthay, Fernando Colchero, Jean-François Lemaître, Louise Maille, Tamás Malkócs, Justus Hagemann, Dalia A Conde, Samuel Pavard and 9 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Indirect genomic effects shape cancer risk across species.bioRxiv : the preprint server for biology · 2026
    Article
  4. 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

19 authors.

Orsolya VinczeUniv. Bordeaux, CNRS, ImmunoConcEpT, UMR 5164, Bordeaux, France. orsolya.vincze@univ-lr.fr.ORCID http://orcid.org/0000-0001-5789-2124
Piotr MiniasDepartment of Biodiversity Studies and Bioeducation, Faculty of Biology and Environmental Protection, University of Łódź, Łódź, Poland.ORCID http://orcid.org/0000-0002-7742-6750
Alexandre CorthayTumor Immunology Lab, Department of Pathology, Rikshospitalet, Oslo University Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0001-9519-5725
Fernando ColcheroDepartment of Primate Behavior and Evolution, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.ORCID http://orcid.org/0000-0001-8613-4568
Jean-François LemaîtreUniversité de Lyon, Université Lyon 1; CNRS, Laboratoire de Biométrie et Biologie Evolutive UMR5558, Villeurbanne, France.
Louise MailleLittoral, Environnement et Sociétés (LIENSs), UMR 7266 CNRS-La Rochelle Université, La Rochelle, France.
Tamás MalkócsLittoral, Environnement et Sociétés (LIENSs), UMR 7266 CNRS-La Rochelle Université, La Rochelle, France.
Justus HagemannLittoral, Environnement et Sociétés (LIENSs), UMR 7266 CNRS-La Rochelle Université, La Rochelle, France.ORCID http://orcid.org/0000-0003-3924-7230
Dalia A CondeInterdisciplinary Centre on Population Dynamics, University of Southern Denmark, Odense, Denmark.
Samuel PavardUnité Eco-Anthropologie (EA), Muséum National d'Histoire Naturelle, CNRS, Université Paris Cité, Paris, France.
Antoine M DujonGeelong, School of Life and Environmental Sciences, Deakin University, Waurn Ponds, VIC, Australia.ORCID http://orcid.org/0000-0002-1579-9156
Beata UjvariGeelong, School of Life and Environmental Sciences, Deakin University, Waurn Ponds, VIC, Australia.ORCID http://orcid.org/0000-0003-2391-2988
Frédéric ThomasCREEC/CANECEV (CREES), MIVEGEC, IRD 224-CNRS 5290-Université de Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0003-2238-1978
Amy M BoddyDepartment of Anthropology, University of California Santa Barbara, Santa Barbara, CA, USA.ORCID http://orcid.org/0000-0002-7990-2415
Carlo C MaleyArizona Cancer Evolution Center, Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ, USA.ORCID http://orcid.org/0000-0002-0745-7076
Damien ChevallierBOREA Research Unit, MNHN, CNRS 8067, SU, IRD 207, UA, Station de recherche marine de Martinique, Les Anses-d'Arlet, France.ORCID http://orcid.org/0000-0002-2232-6787
Tuul SeppInstitute of Ecology and Earth Sciences, University of Tartu, Tartu, Estonia.ORCID http://orcid.org/0000-0002-8677-7069
Thomas Pradeu *Univ. Bordeaux, CNRS, ImmunoConcEpT, UMR 5164, Bordeaux, France.ORCID http://orcid.org/0000-0002-6590-3281
Mathieu Giraudeau *Littoral, Environnement et Sociétés (LIENSs), UMR 7266 CNRS-La Rochelle Université, La Rochelle, France.

Funding

The Role of the Microbiome in Cancer Suppression and Susceptibility Across SpeciesU54CA217376 · NCI · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI MALEY, CARLO · 2018 to 2022
$8.6M
Modeling Neoplastic Progression in Barrett's Esophagus - Renewal -2R01CA140657 · NCI · WISTAR INSTITUTE · PI Carlo Maley · 2009 to 2026
$5.0M
Gordon and Betty Moore Foundation (Gordon E. and Betty I. Moore Foundation) GBMF9021NCI NIH HHS R01 CA140657NCI NIH HHS U54 CA217376
6 · The paper itself

Abstract

Contrary to expectations based on their higher cell numbers, larger and longer-lived species do not face dramatically increased risk of cancer. This strongly suggests that evolution has fashioned natural cancer resistance mechanisms, yet our knowledge remains limited on what these mechanisms might be. The cancer immunological surveillance hypothesis, proposed by Burnet and Thomas in the 1950s, highlights immunity as a key factor determining species-specific cancer resistance. Here we address the original, evolutionary interpretation of this hypothesis by investigating the relationship between cancer mortality risk and markers of efficient antigen presentation. Our results show that the expansion of the MHC class I gene complex, as well as increased selection for diversity at these genes is associated with sharply decreasing cancer mortality risk across mammals. This suggests that the efficient presentation of diverse peptides in somatic cells is important for cancer suppression across mammals, providing pioneering evidence that supports the cancer immunosurveillance hypothesis across species.

Indexed as

Immunologic SurveillanceMammalsNeoplasmsAnimalsAntigen PresentationGenes, MHC Class IHistocompatibility Antigens Class IHumansSpecies SpecificityHistocompatibility Antigens Class I

Identifiers

PMID41285854
PMCPMC12644480

What OpenQuestion holds

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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.