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Variation in the life history strategy underlies functional diversity of tumors
Classical r- vs. K-selection theory describes the trade-offs between high reproductive output and competitiveness and guides research in evolutionary ecology. While its impact has waned in the recent past, cancer evolution may rekindle it. Herein, we impose r- or K-selection on cancer cell lines to...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288455/ https://www.ncbi.nlm.nih.gov/pubmed/34691566 http://dx.doi.org/10.1093/nsr/nwaa124 |
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author | Li, Tao Liu, Jialin Feng, Jing Liu, Zhenzhen Liu, Sixue Zhang, Minjie Zhang, Yuezheng Hou, Yali Wu, Dafei Li, Chunyan Chen, Yongbin Chen, Hua Lu, Xuemei |
author_facet | Li, Tao Liu, Jialin Feng, Jing Liu, Zhenzhen Liu, Sixue Zhang, Minjie Zhang, Yuezheng Hou, Yali Wu, Dafei Li, Chunyan Chen, Yongbin Chen, Hua Lu, Xuemei |
author_sort | Li, Tao |
collection | PubMed |
description | Classical r- vs. K-selection theory describes the trade-offs between high reproductive output and competitiveness and guides research in evolutionary ecology. While its impact has waned in the recent past, cancer evolution may rekindle it. Herein, we impose r- or K-selection on cancer cell lines to obtain strongly proliferative r cells and highly competitive K cells to test ideas on life-history strategy evolution. RNA-seq indicates that the trade-offs are associated with distinct expression of genes involved in the cell cycle, adhesion, apoptosis, and contact inhibition. Both empirical observations and simulations based on an ecological competition model show that the trade-off between cell proliferation and competitiveness can evolve adaptively. When the r and K cells are mixed, they exhibit strikingly different spatial and temporal distributions. Due to this niche separation, the fitness of the entire tumor increases. The contrasting selective pressure may operate in a realistic ecological setting of actual tumors. |
format | Online Article Text |
id | pubmed-8288455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82884552021-10-21 Variation in the life history strategy underlies functional diversity of tumors Li, Tao Liu, Jialin Feng, Jing Liu, Zhenzhen Liu, Sixue Zhang, Minjie Zhang, Yuezheng Hou, Yali Wu, Dafei Li, Chunyan Chen, Yongbin Chen, Hua Lu, Xuemei Natl Sci Rev Biology & Biochemistry Classical r- vs. K-selection theory describes the trade-offs between high reproductive output and competitiveness and guides research in evolutionary ecology. While its impact has waned in the recent past, cancer evolution may rekindle it. Herein, we impose r- or K-selection on cancer cell lines to obtain strongly proliferative r cells and highly competitive K cells to test ideas on life-history strategy evolution. RNA-seq indicates that the trade-offs are associated with distinct expression of genes involved in the cell cycle, adhesion, apoptosis, and contact inhibition. Both empirical observations and simulations based on an ecological competition model show that the trade-off between cell proliferation and competitiveness can evolve adaptively. When the r and K cells are mixed, they exhibit strikingly different spatial and temporal distributions. Due to this niche separation, the fitness of the entire tumor increases. The contrasting selective pressure may operate in a realistic ecological setting of actual tumors. Oxford University Press 2020-06-05 /pmc/articles/PMC8288455/ /pubmed/34691566 http://dx.doi.org/10.1093/nsr/nwaa124 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biology & Biochemistry Li, Tao Liu, Jialin Feng, Jing Liu, Zhenzhen Liu, Sixue Zhang, Minjie Zhang, Yuezheng Hou, Yali Wu, Dafei Li, Chunyan Chen, Yongbin Chen, Hua Lu, Xuemei Variation in the life history strategy underlies functional diversity of tumors |
title | Variation in the life history strategy underlies functional diversity of tumors |
title_full | Variation in the life history strategy underlies functional diversity of tumors |
title_fullStr | Variation in the life history strategy underlies functional diversity of tumors |
title_full_unstemmed | Variation in the life history strategy underlies functional diversity of tumors |
title_short | Variation in the life history strategy underlies functional diversity of tumors |
title_sort | variation in the life history strategy underlies functional diversity of tumors |
topic | Biology & Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288455/ https://www.ncbi.nlm.nih.gov/pubmed/34691566 http://dx.doi.org/10.1093/nsr/nwaa124 |
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