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Polyploidy as an Adaptation against Loss of Heterozygosity in Cancer

Polyploidy is common in cancer cells and has implications for tumor progression and resistance to therapies, but it is unclear whether it is an adaptation of the tumor or the non-adaptive effect of genomic instability. I discuss the possibility that polyploidy reduces the deleterious effects of loss...

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Autor principal: Archetti, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369199/
https://www.ncbi.nlm.nih.gov/pubmed/35955663
http://dx.doi.org/10.3390/ijms23158528
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author Archetti, Marco
author_facet Archetti, Marco
author_sort Archetti, Marco
collection PubMed
description Polyploidy is common in cancer cells and has implications for tumor progression and resistance to therapies, but it is unclear whether it is an adaptation of the tumor or the non-adaptive effect of genomic instability. I discuss the possibility that polyploidy reduces the deleterious effects of loss of heterozygosity, which arises as a consequence of mitotic recombination, and which in diploid cells leads instead to the rapid loss of complementation of recessive deleterious mutations. I use computational predictions of loss of heterozygosity to show that a population of diploid cells dividing by mitosis with recombination can be easily invaded by mutant polyploid cells or cells that divide by endomitosis, which reduces loss of complementation, or by mutant cells that occasionally fuse, which restores heterozygosity. A similar selective advantage of polyploidy has been shown for the evolution of different types of asexual reproduction in nature. This provides an adaptive explanation for cyclical ploidy, mitotic slippage and cell fusion in cancer cells.
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spelling pubmed-93691992022-08-12 Polyploidy as an Adaptation against Loss of Heterozygosity in Cancer Archetti, Marco Int J Mol Sci Article Polyploidy is common in cancer cells and has implications for tumor progression and resistance to therapies, but it is unclear whether it is an adaptation of the tumor or the non-adaptive effect of genomic instability. I discuss the possibility that polyploidy reduces the deleterious effects of loss of heterozygosity, which arises as a consequence of mitotic recombination, and which in diploid cells leads instead to the rapid loss of complementation of recessive deleterious mutations. I use computational predictions of loss of heterozygosity to show that a population of diploid cells dividing by mitosis with recombination can be easily invaded by mutant polyploid cells or cells that divide by endomitosis, which reduces loss of complementation, or by mutant cells that occasionally fuse, which restores heterozygosity. A similar selective advantage of polyploidy has been shown for the evolution of different types of asexual reproduction in nature. This provides an adaptive explanation for cyclical ploidy, mitotic slippage and cell fusion in cancer cells. MDPI 2022-08-01 /pmc/articles/PMC9369199/ /pubmed/35955663 http://dx.doi.org/10.3390/ijms23158528 Text en © 2022 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Archetti, Marco
Polyploidy as an Adaptation against Loss of Heterozygosity in Cancer
title Polyploidy as an Adaptation against Loss of Heterozygosity in Cancer
title_full Polyploidy as an Adaptation against Loss of Heterozygosity in Cancer
title_fullStr Polyploidy as an Adaptation against Loss of Heterozygosity in Cancer
title_full_unstemmed Polyploidy as an Adaptation against Loss of Heterozygosity in Cancer
title_short Polyploidy as an Adaptation against Loss of Heterozygosity in Cancer
title_sort polyploidy as an adaptation against loss of heterozygosity in cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369199/
https://www.ncbi.nlm.nih.gov/pubmed/35955663
http://dx.doi.org/10.3390/ijms23158528
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