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. 2010 Dec 7;104(1):91–100. doi: 10.1038/sj.bjc.6606007

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Copyright © 2011 Cancer Research UK

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GUT-70-induced cell growth inhibition, apoptosis, and cell cycle arrest in MCL. (A) JVM-2, Granta 519, Jeko-1, and MINO cells were treated with the indicated concentrations of GUT-70 for 48 h, and the percentages of apoptotic cells were quantified by annexin V/PI staining. (B) Representative flow cytometric histograms of PI-treated cells after 24 h of GUT-70 treatment at indicated concentrations. The percentages of G₀/G₁-, S- and G₂/M-phase cells were assessed in total viable cells (bar graphs).

GUT-70-induced cell growth inhibition, apoptosis, and cell cycle arrest in MCL. (A) JVM-2, Granta 519, Jeko-1, and MINO cells were treated with the indicated concentrations of GUT-70 for 48 h, and the percentages of apoptotic cells were quantified by annexin V/PI staining. (B) Representative flow cytometric histograms of PI-treated cells after 24 h of GUT-70 treatment at indicated concentrations. The percentages of G₀/G₁-, S- and G₂/M-phase cells were assessed in total viable cells (bar graphs).