BioMed Research International · 2014 · 29 citations · 28 references
Life SciencesCell BiologyMolecular BiologyCell DivisionGene ExpressionMolecular OncologyCell Cycle ControlCell Cycle Gene RegulationCell Cycle TransitionsCell-cycle ArrestCell-cycle RegulationCyclin-dependent KinasesCancer-associated Cyclin-dependent KinasesCell Cycle Control ProteinsCell Cycle DynamicsCell Cycle InhibitionEzh2 FunctionP21 RegulationProtein Expression LevelsWestern Blotting
Nonsmall-cell lung cancer has a high mortality rate and poor prognosis. In the present study, we silenced EZH2 and explored the consequent cell cycle changes. The expression of cell-cycle-related proteins, including p53, p21, Cdc2, and cyclin B1, was detected with western blotting, and the cell cycle distribution was determined with flow cytometry. Inhibition of EZH2 expression changed the cell cycle distribution, in particular inducing G2/M arrest. Expression of Cdc2 and cyclin B1 was significantly decreased in A549 and HTB-56 cells after EZH2-siRNA treatment. In addition, p53 expression was increased by 21% and 18%, and p21 expression was increased by 31% and 23%, in A549 and HTB-56 cells, respectively, in the presence of EZH2-siRNA. This study clearly demonstrates that modulation of EZH2 expression with siRNA affects the cell cycle and the expression levels of p53 and p21, thereby changing cyclin B1 and Cdc2 expression and inducing G2/M arrest. These results may explain the observed antitumor activity of EZH2 silencing. Such explorations of the molecular mechanism of EZH2 will help us develop novel approaches to the diagnosis, treatment, and prevention of nonsmall-cell lung cancer.
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EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2-activating mutations
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