Germline mutation rate predicts cancer mortality across 37 vertebrate species.

animals germ cell mutations malignancy tumor

Journal

Evolution, medicine, and public health
ISSN: 2050-6201
Titre abrégé: Evol Med Public Health
Pays: England
ID NLM: 101616698

Informations de publication

Date de publication:
2024
Historique:
received: 03 10 2023
revised: 05 08 2024
medline: 5 9 2024
pubmed: 5 9 2024
entrez: 5 9 2024
Statut: epublish

Résumé

Cancer develops across nearly every species. However, cancer occurs at unexpected and widely different rates throughout the animal kingdom. The reason for this variation in cancer susceptibility remains an area of intense investigation. Cancer evolves in part through the accumulation of mutations, and therefore, we hypothesized that germline mutation rates would be associated with cancer prevalence and mortality across species. We collected previously published data on germline mutation rate and cancer mortality data for 37 vertebrate species. Germline mutation rate was positively correlated with cancer mortality (P-value = 0.0008; R2 = 0.13). Controlling for species' average parental age, maximum longevity, adult body mass or domestication did not improve the model fit (the change (Δ) in Akaike Information Criterion (AIC) was less than 2). However, this model fit was better than a model controlling for species trophic level (ΔAIC > 2). The increased death rate from cancer in animals with increased germline mutation rates may suggest underlying hereditary cancer predisposition syndromes similar to those diagnosed in human patients. Species with higher germline mutation rates may benefit from close monitoring for tumors due to increased genetic risk for cancer development. Early diagnoses of cancer in these species may increase their chances of overall survival, especially for threatened and endangered species.

Sections du résumé

Background and objectives UNASSIGNED
Cancer develops across nearly every species. However, cancer occurs at unexpected and widely different rates throughout the animal kingdom. The reason for this variation in cancer susceptibility remains an area of intense investigation. Cancer evolves in part through the accumulation of mutations, and therefore, we hypothesized that germline mutation rates would be associated with cancer prevalence and mortality across species.
Methodology UNASSIGNED
We collected previously published data on germline mutation rate and cancer mortality data for 37 vertebrate species.
Results UNASSIGNED
Germline mutation rate was positively correlated with cancer mortality (P-value = 0.0008; R2 = 0.13). Controlling for species' average parental age, maximum longevity, adult body mass or domestication did not improve the model fit (the change (Δ) in Akaike Information Criterion (AIC) was less than 2). However, this model fit was better than a model controlling for species trophic level (ΔAIC > 2).
Conclusions and implications UNASSIGNED
The increased death rate from cancer in animals with increased germline mutation rates may suggest underlying hereditary cancer predisposition syndromes similar to those diagnosed in human patients. Species with higher germline mutation rates may benefit from close monitoring for tumors due to increased genetic risk for cancer development. Early diagnoses of cancer in these species may increase their chances of overall survival, especially for threatened and endangered species.

Identifiants

pubmed: 39233763
doi: 10.1093/emph/eoae016
pii: eoae016
pmc: PMC11372239
doi:

Types de publication

Journal Article

Langues

eng

Pagination

122-128

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health.

Déclaration de conflit d'intérêts

J.D.S. is a co-founder and shareholder employed by Peel Therapeutics, Inc., and L.M.A. is a shareholder and consultant to Peel Therapeutics, Inc.

Auteurs

Stefania E Kapsetaki (SE)

Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
Center for Biocomputing, Security and Society, Biodesign Institute, Arizona State University, Tempe, AZ, USA.
Department of Biology, School of Arts and Sciences, Tufts University, Medford, MA, USA.

Zachary T Compton (ZT)

Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
University of Arizona Cancer Center, Tucson, AZ, USA.
University of Arizona College of Medicine, Tucson, AZ, USA.

Walker Mellon (W)

Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.

Orsolya Vincze (O)

Evolutionary Ecology Group, Hungarian Department of Biology and Ecology, Babeș-Bolyai University, Cluj-Napoca, Romania.
Institute of Aquatic Ecology, Centre for Ecological Research, Debrecen, Hungary.

Mathieu Giraudeau (M)

Littoral Environnement Et Sociétés (LIENSs), UMR7266, CNRS Université de La Rochelle, 2 rue Olympe de Gouges, 17042 La Rochelle Cedex, France.

Tara M Harrison (TM)

Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
Department of Clinical Sciences, North Carolina State University, Raleigh, NC 27607, USA.
Exotic Species Cancer Research Alliance, North Carolina State University, Raleigh, NC 27607, USA.

Lisa M Abegglen (LM)

Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
Exotic Species Cancer Research Alliance, North Carolina State University, Raleigh, NC 27607, USA.
Department of Pediatrics and Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Peel Therapeutics, Inc., Salt Lake City, UT, USA.

Amy M Boddy (AM)

Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
Exotic Species Cancer Research Alliance, North Carolina State University, Raleigh, NC 27607, USA.
Department of Anthropology, University of California Santa Barbara, Santa Barbara, CA, USA.

Carlo C Maley (CC)

Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
Center for Biocomputing, Security and Society, Biodesign Institute, Arizona State University, Tempe, AZ, USA.
School of Life Sciences, Arizona State University, Tempe, AZ, USA.

Joshua D Schiffman (JD)

Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
Department of Pediatrics and Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Peel Therapeutics, Inc., Salt Lake City, UT, USA.

Classifications MeSH