A new perspective on tumor progression: Evolution via selection for function.

evolution function group phenotypic composition perspective progression selection tumors

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: 22 03 2024
revised: 02 09 2024
medline: 4 10 2024
pubmed: 4 10 2024
entrez: 4 10 2024
Statut: epublish

Résumé

Tumorigenesis is commonly attributed to Darwinian processes involving natural selection among cells and groups of cells. However, progressing tumors are those that also achieve an appropriate group phenotypic composition (GPC). Yet, the selective processes acting on tumor GPCs are distinct from that associated with classical Darwinian evolution (i.e. natural selection based on differential reproductive success) as tumors are not genuine evolutionary individuals and do not exhibit heritable variation in fitness. This complex evolutionary scenario is analogous to the recently proposed concept of 'selection for function' invoked for the evolution of both living and non-living systems. Therefore, we argue that it is inaccurate to assert that Darwinian processes alone account for all the aspects characterizing tumorigenesis and cancer progression; rather, by producing the genetic and phenotypic diversity required for creating novel GPCs, these processes fuel the evolutionary success of tumors that is dependent on selection for function at the tumor level.

Identifiants

pubmed: 39364294
doi: 10.1093/emph/eoae021
pii: eoae021
pmc: PMC11448472
doi:

Types de publication

Journal Article

Langues

eng

Pagination

172-177

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

None declared.

Auteurs

Frédéric Thomas (F)

CREEC/CANECEV, MIVEGEC (CREES) Department, University of Montpellier, CNRS, IRD, Montpellier, France.

James DeGregori (J)

Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Andriy Marusyk (A)

Department of Cancer Physiology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

Antoine M Dujon (AM)

CREEC/CANECEV, MIVEGEC (CREES) Department, University of Montpellier, CNRS, IRD, Montpellier, France.
School of Life and Environmental Sciences, Deakin University, Geelong, Centre for Integrative Ecology, Waurn Ponds, VIC 3216, Australia.

Beata Ujvari (B)

School of Life and Environmental Sciences, Deakin University, Geelong, Centre for Integrative Ecology, Waurn Ponds, VIC 3216, Australia.

Jean-Pascal Capp (JP)

Toulouse Biotechnology Institute, University of Toulouse, INSA, CNRS, INRAE, Toulouse, France.

Robert Gatenby (R)

Department of Cancer Physiology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

Aurora M Nedelcu (AM)

Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada.

Classifications MeSH