The three dimensions of somatic evolution: Integrating the role of genetic damage, life‐history traits, and aging in carcinogenesis
Abstract Tumors result from genetic and epigenetic alterations that change cellular survival and differentiation probabilities, promoting clonal dominance. Subsequent genetic and selection processes in tumors allow cells to lose their tissue fidelity and migrate to other parts of the body, turning t...
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Online Access: | https://doi.org/10.1111/eva.12947 |
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doaj-1b368865b3f64151ac4c8aab21838ae32020-11-25T03:22:02ZengWileyEvolutionary Applications1752-45712020-08-011371569158010.1111/eva.12947The three dimensions of somatic evolution: Integrating the role of genetic damage, life‐history traits, and aging in carcinogenesisAndrii I. Rozhok0James DeGregori1Department of Biochemistry and Molecular Genetics University of Colorado Anschutz Medical Campus Aurora ColoradoDepartment of Biochemistry and Molecular Genetics University of Colorado Anschutz Medical Campus Aurora ColoradoAbstract Tumors result from genetic and epigenetic alterations that change cellular survival and differentiation probabilities, promoting clonal dominance. Subsequent genetic and selection processes in tumors allow cells to lose their tissue fidelity and migrate to other parts of the body, turning tumors into cancer. However, the relationship between genetic damage and cancer is not linear, showing remarkable and sometimes seemingly counterintuitive patterns for different tissues and across animal taxa. In the present paper, we attempt to integrate our understanding of somatic evolution and cancer as a product of three major orthogonal processes: occurrence of somatic mutations, evolution of species‐specific life‐history traits, and physiological aging. Patterns of cancer risk have been shaped by selective pressures experienced by animal populations over millions of years, influencing and influenced by selection acting on traits ranging from mutation rate to reproductive strategies to longevity. We discuss how evolution of species shapes their cancer profiles alongside and in connection with other evolving life‐history traits and how this process explains the patterns of cancer incidence we observe in humans and other animals.https://doi.org/10.1111/eva.12947carcinogenesislife‐history evolutionlongevitysomatic evolution |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andrii I. Rozhok James DeGregori |
spellingShingle |
Andrii I. Rozhok James DeGregori The three dimensions of somatic evolution: Integrating the role of genetic damage, life‐history traits, and aging in carcinogenesis Evolutionary Applications carcinogenesis life‐history evolution longevity somatic evolution |
author_facet |
Andrii I. Rozhok James DeGregori |
author_sort |
Andrii I. Rozhok |
title |
The three dimensions of somatic evolution: Integrating the role of genetic damage, life‐history traits, and aging in carcinogenesis |
title_short |
The three dimensions of somatic evolution: Integrating the role of genetic damage, life‐history traits, and aging in carcinogenesis |
title_full |
The three dimensions of somatic evolution: Integrating the role of genetic damage, life‐history traits, and aging in carcinogenesis |
title_fullStr |
The three dimensions of somatic evolution: Integrating the role of genetic damage, life‐history traits, and aging in carcinogenesis |
title_full_unstemmed |
The three dimensions of somatic evolution: Integrating the role of genetic damage, life‐history traits, and aging in carcinogenesis |
title_sort |
three dimensions of somatic evolution: integrating the role of genetic damage, life‐history traits, and aging in carcinogenesis |
publisher |
Wiley |
series |
Evolutionary Applications |
issn |
1752-4571 |
publishDate |
2020-08-01 |
description |
Abstract Tumors result from genetic and epigenetic alterations that change cellular survival and differentiation probabilities, promoting clonal dominance. Subsequent genetic and selection processes in tumors allow cells to lose their tissue fidelity and migrate to other parts of the body, turning tumors into cancer. However, the relationship between genetic damage and cancer is not linear, showing remarkable and sometimes seemingly counterintuitive patterns for different tissues and across animal taxa. In the present paper, we attempt to integrate our understanding of somatic evolution and cancer as a product of three major orthogonal processes: occurrence of somatic mutations, evolution of species‐specific life‐history traits, and physiological aging. Patterns of cancer risk have been shaped by selective pressures experienced by animal populations over millions of years, influencing and influenced by selection acting on traits ranging from mutation rate to reproductive strategies to longevity. We discuss how evolution of species shapes their cancer profiles alongside and in connection with other evolving life‐history traits and how this process explains the patterns of cancer incidence we observe in humans and other animals. |
topic |
carcinogenesis life‐history evolution longevity somatic evolution |
url |
https://doi.org/10.1111/eva.12947 |
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