Figure 3.
Figure 3. Induction of p53-related proteins by F-ara-A and Nutlin-3a in a CLL sample with wild-type p53. The sample contained more than 95% CD5+CD19+ cells with normal Atm levels. Cells were treated with 5 μM F-ara-A (F) and 5 μM Nutlin-3a (3a) either as individual agents or in combination, for the indicated times. F-ara-A induced p53 phosphorylation on Ser15, followed by p53 accumulation and Puma induction. Nutlin-3a induced immediate accumulation of p53 that is mostly free of phosphorylation on Ser15, followed by Mdm2 and Puma induction. The degree of Puma induction was further enhanced in cells treated with F-ara-A and Nutlin-3a. β-Actin is used to confirm equal loading of proteins. Lysate from cells before treatment served as control (C).

Induction of p53-related proteins by F-ara-A and Nutlin-3a in a CLL sample with wild-type p53. The sample contained more than 95% CD5+CD19+ cells with normal Atm levels. Cells were treated with 5 μM F-ara-A (F) and 5 μM Nutlin-3a (3a) either as individual agents or in combination, for the indicated times. F-ara-A induced p53 phosphorylation on Ser15 , followed by p53 accumulation and Puma induction. Nutlin-3a induced immediate accumulation of p53 that is mostly free of phosphorylation on Ser15 , followed by Mdm2 and Puma induction. The degree of Puma induction was further enhanced in cells treated with F-ara-A and Nutlin-3a. β-Actin is used to confirm equal loading of proteins. Lysate from cells before treatment served as control (C).

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