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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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.
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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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