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Selective advantage of trisomic human cells cultured in non-standard conditions

An abnormal chromosome number, a condition known as aneuploidy, is a ubiquitous feature of cancer cells. A number of studies have shown that aneuploidy impairs cellular fitness. However, there is also evidence that aneuploidy can arise in response to specific challenges and can confer a selective ad...

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Autores principales: Rutledge, Samuel D., Douglas, Temple A., Nicholson, Joshua M., Vila-Casadesús, Maria, Kantzler, Courtney L., Wangsa, Darawalee, Barroso-Vilares, Monika, Kale, Shiv D., Logarinho, Elsa, Cimini, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783771/
https://www.ncbi.nlm.nih.gov/pubmed/26956415
http://dx.doi.org/10.1038/srep22828
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author Rutledge, Samuel D.
Douglas, Temple A.
Nicholson, Joshua M.
Vila-Casadesús, Maria
Kantzler, Courtney L.
Wangsa, Darawalee
Barroso-Vilares, Monika
Kale, Shiv D.
Logarinho, Elsa
Cimini, Daniela
author_facet Rutledge, Samuel D.
Douglas, Temple A.
Nicholson, Joshua M.
Vila-Casadesús, Maria
Kantzler, Courtney L.
Wangsa, Darawalee
Barroso-Vilares, Monika
Kale, Shiv D.
Logarinho, Elsa
Cimini, Daniela
author_sort Rutledge, Samuel D.
collection PubMed
description An abnormal chromosome number, a condition known as aneuploidy, is a ubiquitous feature of cancer cells. A number of studies have shown that aneuploidy impairs cellular fitness. However, there is also evidence that aneuploidy can arise in response to specific challenges and can confer a selective advantage under certain environmental stresses. Cancer cells are likely exposed to a number of challenging conditions arising within the tumor microenvironment. To investigate whether aneuploidy may confer a selective advantage to cancer cells, we employed a controlled experimental system. We used the diploid, colorectal cancer cell line DLD1 and two DLD1-derived cell lines carrying single-chromosome aneuploidies to assess a number of cancer cell properties. Such properties, which included rates of proliferation and apoptosis, anchorage-independent growth, and invasiveness, were assessed both under standard culture conditions and under conditions of stress (i.e., serum starvation, drug treatment, hypoxia). Similar experiments were performed in diploid vs. aneuploid non-transformed human primary cells. Overall, our data show that aneuploidy can confer selective advantage to human cells cultured under non-standard conditions. These findings indicate that aneuploidy can increase the adaptability of cells, even those, such as cancer cells, that are already characterized by increased proliferative capacity and aggressive tumorigenic phenotypes.
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spelling pubmed-47837712016-03-11 Selective advantage of trisomic human cells cultured in non-standard conditions Rutledge, Samuel D. Douglas, Temple A. Nicholson, Joshua M. Vila-Casadesús, Maria Kantzler, Courtney L. Wangsa, Darawalee Barroso-Vilares, Monika Kale, Shiv D. Logarinho, Elsa Cimini, Daniela Sci Rep Article An abnormal chromosome number, a condition known as aneuploidy, is a ubiquitous feature of cancer cells. A number of studies have shown that aneuploidy impairs cellular fitness. However, there is also evidence that aneuploidy can arise in response to specific challenges and can confer a selective advantage under certain environmental stresses. Cancer cells are likely exposed to a number of challenging conditions arising within the tumor microenvironment. To investigate whether aneuploidy may confer a selective advantage to cancer cells, we employed a controlled experimental system. We used the diploid, colorectal cancer cell line DLD1 and two DLD1-derived cell lines carrying single-chromosome aneuploidies to assess a number of cancer cell properties. Such properties, which included rates of proliferation and apoptosis, anchorage-independent growth, and invasiveness, were assessed both under standard culture conditions and under conditions of stress (i.e., serum starvation, drug treatment, hypoxia). Similar experiments were performed in diploid vs. aneuploid non-transformed human primary cells. Overall, our data show that aneuploidy can confer selective advantage to human cells cultured under non-standard conditions. These findings indicate that aneuploidy can increase the adaptability of cells, even those, such as cancer cells, that are already characterized by increased proliferative capacity and aggressive tumorigenic phenotypes. Nature Publishing Group 2016-03-09 /pmc/articles/PMC4783771/ /pubmed/26956415 http://dx.doi.org/10.1038/srep22828 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Rutledge, Samuel D.
Douglas, Temple A.
Nicholson, Joshua M.
Vila-Casadesús, Maria
Kantzler, Courtney L.
Wangsa, Darawalee
Barroso-Vilares, Monika
Kale, Shiv D.
Logarinho, Elsa
Cimini, Daniela
Selective advantage of trisomic human cells cultured in non-standard conditions
title Selective advantage of trisomic human cells cultured in non-standard conditions
title_full Selective advantage of trisomic human cells cultured in non-standard conditions
title_fullStr Selective advantage of trisomic human cells cultured in non-standard conditions
title_full_unstemmed Selective advantage of trisomic human cells cultured in non-standard conditions
title_short Selective advantage of trisomic human cells cultured in non-standard conditions
title_sort selective advantage of trisomic human cells cultured in non-standard conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783771/
https://www.ncbi.nlm.nih.gov/pubmed/26956415
http://dx.doi.org/10.1038/srep22828
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