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.
Highlights
Adjusting rates of cell proliferation is the objective of many therapeutic strategies
We monitored the effects of each drug on cell cycle progression by measuring the DNA content of the cells by flow cytometry [7]
We re-tested the ‘‘High G1’’ drugs by adding them to actively dividing cells. From this primary analysis we identified 27 compounds that interfered with progression in the G1 phase of the cell cycle, before initiation of DNA replication, resulting in a ‘‘High G1’’ DNA content
Summary
Adjusting rates of cell proliferation is the objective of many therapeutic strategies. We monitored the effects of each drug on cell cycle progression by measuring the DNA content of the cells by flow cytometry [7] (see Figure 1, and Materials and Methods). Drugs in samples with a ‘‘High G1’’ DNA content may have arrested cell cycle progression non-.
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