The Cellular Stress Responses and the Resolution of Peto's Paradox

Peto's paradox (Pp) results from the evidence that in mammals there is no obvious positive correlation between body size, lifespan, and cancer incidence. Posing the question of which mechanisms are responsible for this. Comparative studies searching for specific anticancer mechanisms as putative solutions to Pp have been undertaken in mammals. The result of these efforts are further inconsistencies leading to ad-hoc hypotheses and unnecessary complexity. In contrast to this, we present evidence that the cellular stress responses (CSRs), aimed at curtailing proteotoxic stress and assuring cell survival are necessary for enabling carcinogenesis. Yet, natural selection adjusts the performance of the CSRs according to the life history of each species and because of this, cancer is mostly delayed to the post-reproductive stage in all mammalian species, resulting in a limited impact of cancer on species fitness and viability. From this perspective, the need of evolving anticancer mechanisms, suggested by Pp is weakened or disappears and the paradox is likely resolved.

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Publication Details

Journal
BioEssays
Published
2026-03-31
DOI
https://doi.org/10.1002/bies.70131
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
0.00
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article

The Cellular Stress Responses and the Resolution of Peto's Paradox

Armando Aranda‐Anzaldo, Edith Segura‐Anaya, Myrna A. R. Dent, Alejandro Martínez‐Gómez
BioEssays
Genetics, Aging, and Longevity in Model Organisms
article

The Cellular Stress Responses and the Resolution of Peto's Paradox

Armando Aranda‐Anzaldo, Edith Segura‐Anaya, Myrna A. R. Dent, Alejandro Martínez‐Gómez
article en

Abstract

Peto's paradox (Pp) results from the evidence that in mammals there is no obvious positive correlation between body size, lifespan, and cancer incidence. Posing the question of which mechanisms are responsible for this. Comparative studies searching for specific anticancer mechanisms as putative solutions to Pp have been undertaken in mammals. The result of these efforts are further inconsistencies leading to ad-hoc hypotheses and unnecessary complexity. In contrast to this, we present evidence that the cellular stress responses (CSRs), aimed at curtailing proteotoxic stress and assuring cell survival are necessary for enabling carcinogenesis. Yet, natural selection adjusts the performance of the CSRs according to the life history of each species and because of this, cancer is mostly delayed to the post-reproductive stage in all mammalian species, resulting in a limited impact of cancer on species fitness and viability. From this perspective, the need of evolving anticancer mechanisms, suggested by Pp is weakened or disappears and the paradox is likely resolved.

BioEssaysVol. 48(4)
Universidad Autónoma del Estado de México (MX)
Openalex Percentile: Top 11%
Genetics, Aging, and Longevity in Model Organisms
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