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Systematic Analysis of Cell Cycle Effects of Common Drugs Leads to the Discovery of a Suppressive Interaction between Gemfibrozil and Fluoxetine
Screening chemical libraries to identify compounds that affect overall cell proliferation is common. However, in most cases, it is not known whether the compounds tested alter the timing of particular cell cycle transitions. Here, we evaluated an FDA-approved drug library to identify pharmaceuticals...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342239/ https://www.ncbi.nlm.nih.gov/pubmed/22567160 http://dx.doi.org/10.1371/journal.pone.0036503 |
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author | Hoose, Scott A. Duran, Camille Malik, Indranil Eslamfam, Shabnam Shasserre, Samantha C. Downing, S. Sabina Hoover, Evelyn M. Dowd, Katherine E. Smith, Roger Polymenis, Michael |
author_facet | Hoose, Scott A. Duran, Camille Malik, Indranil Eslamfam, Shabnam Shasserre, Samantha C. Downing, S. Sabina Hoover, Evelyn M. Dowd, Katherine E. Smith, Roger Polymenis, Michael |
author_sort | Hoose, Scott A. |
collection | PubMed |
description | Screening chemical libraries to identify compounds that affect overall cell proliferation is common. However, in most cases, it is not known whether the compounds tested alter the timing of particular cell cycle transitions. Here, we evaluated an FDA-approved drug library to identify pharmaceuticals that alter cell cycle progression in yeast, using DNA content measurements by flow cytometry. This approach revealed strong cell cycle effects of several commonly used pharmaceuticals. We show that the antilipemic gemfibrozil delays initiation of DNA replication, while cells treated with the antidepressant fluoxetine severely delay progression through mitosis. Based on their effects on cell cycle progression, we also examined cell proliferation in the presence of both compounds. We discovered a strong suppressive interaction between gemfibrozil and fluoxetine. Combinations of interest among diverse pharmaceuticals are difficult to identify, due to the daunting number of possible combinations that must be evaluated. The novel interaction between gemfibrozil and fluoxetine suggests that identifying and combining drugs that show cell cycle effects might streamline identification of drug combinations with a pronounced impact on cell proliferation. |
format | Online Article Text |
id | pubmed-3342239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33422392012-05-07 Systematic Analysis of Cell Cycle Effects of Common Drugs Leads to the Discovery of a Suppressive Interaction between Gemfibrozil and Fluoxetine Hoose, Scott A. Duran, Camille Malik, Indranil Eslamfam, Shabnam Shasserre, Samantha C. Downing, S. Sabina Hoover, Evelyn M. Dowd, Katherine E. Smith, Roger Polymenis, Michael PLoS One Research Article Screening chemical libraries to identify compounds that affect overall cell proliferation is common. However, in most cases, it is not known whether the compounds tested alter the timing of particular cell cycle transitions. Here, we evaluated an FDA-approved drug library to identify pharmaceuticals that alter cell cycle progression in yeast, using DNA content measurements by flow cytometry. This approach revealed strong cell cycle effects of several commonly used pharmaceuticals. We show that the antilipemic gemfibrozil delays initiation of DNA replication, while cells treated with the antidepressant fluoxetine severely delay progression through mitosis. Based on their effects on cell cycle progression, we also examined cell proliferation in the presence of both compounds. We discovered a strong suppressive interaction between gemfibrozil and fluoxetine. Combinations of interest among diverse pharmaceuticals are difficult to identify, due to the daunting number of possible combinations that must be evaluated. The novel interaction between gemfibrozil and fluoxetine suggests that identifying and combining drugs that show cell cycle effects might streamline identification of drug combinations with a pronounced impact on cell proliferation. Public Library of Science 2012-05-02 /pmc/articles/PMC3342239/ /pubmed/22567160 http://dx.doi.org/10.1371/journal.pone.0036503 Text en Hoose et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hoose, Scott A. Duran, Camille Malik, Indranil Eslamfam, Shabnam Shasserre, Samantha C. Downing, S. Sabina Hoover, Evelyn M. Dowd, Katherine E. Smith, Roger Polymenis, Michael Systematic Analysis of Cell Cycle Effects of Common Drugs Leads to the Discovery of a Suppressive Interaction between Gemfibrozil and Fluoxetine |
title | Systematic Analysis of Cell Cycle Effects of Common Drugs Leads to the Discovery of a Suppressive Interaction between Gemfibrozil and Fluoxetine |
title_full | Systematic Analysis of Cell Cycle Effects of Common Drugs Leads to the Discovery of a Suppressive Interaction between Gemfibrozil and Fluoxetine |
title_fullStr | Systematic Analysis of Cell Cycle Effects of Common Drugs Leads to the Discovery of a Suppressive Interaction between Gemfibrozil and Fluoxetine |
title_full_unstemmed | Systematic Analysis of Cell Cycle Effects of Common Drugs Leads to the Discovery of a Suppressive Interaction between Gemfibrozil and Fluoxetine |
title_short | Systematic Analysis of Cell Cycle Effects of Common Drugs Leads to the Discovery of a Suppressive Interaction between Gemfibrozil and Fluoxetine |
title_sort | systematic analysis of cell cycle effects of common drugs leads to the discovery of a suppressive interaction between gemfibrozil and fluoxetine |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342239/ https://www.ncbi.nlm.nih.gov/pubmed/22567160 http://dx.doi.org/10.1371/journal.pone.0036503 |
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