AI Article Synopsis

  • Screening chemical libraries to find compounds affecting cell proliferation is common, but it’s often unclear how those compounds impact specific cell cycle transitions.
  • Researchers tested an FDA-approved drug library on yeast to see how different pharmaceuticals influence cell cycle progression, finding significant effects from drugs like gemfibrozil and fluoxetine.
  • The study highlights a unique interaction between gemfibrozil, which delays DNA replication, and fluoxetine, which stalls mitosis, suggesting that exploring drug combinations could help in identifying effective treatments that alter cell proliferation.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342239PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0036503PLOS

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