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PNAS 103 (6): 1888-1893

Copyright © 2006 by the National Academy of Sciences.

Small-molecule MDM2 antagonists reveal aberrant p53 signaling in cancer: Implications for therapy

Christian Tovar*,{dagger}, James Rosinski*,{dagger}, Zoran Filipovic*, Brian Higgins*, Kenneth Kolinsky*, Holly Hilton*, Xiaolan Zhao*, Binh T. Vu*, Weiguo Qing*, Kathryn Packman*, Ola Myklebost{ddagger}, David C. Heimbrook*, and Lyubomir T. Vassilev*,

*Roche Research Center, Hoffmann-La Roche Inc., Nutley, NJ 07110; and {ddagger}Institute for Cancer Research, Norwegian Radium Hospital, 0310 Oslo, Norway


Figure 1
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Fig. 1. Nutlin-3 selectively activates p53. (A) Exponentially growing mouse NIH/3T3 fibroblasts (wt-TP53) and MEFs from TP53–/–/mdm2–/– knockout mice were incubated for 7 days in the presence of nutlin-3a and stained live by acridine orange. (B) Exponentially growing cells were treated with nutlin-3a for 5 days, and their viability was measured in three independent samples by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay and expressed as percentage of control SD. (C) A heat map of probe sets differentially expressed between nutlin-3a and all other treatments (3-fold changed, t test P < 0.05 vs. untreated cells) represented as the median normalized expression of the condition. Red indicates higher than median expression; green indicates lower than median expression. Data were generated on Affymetrix HG-U133 Genechips. (D) A heat map of the same probe sets displayed as a ratio of the treated condition vs. the untreated control.

 

Figure 2
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Fig. 2. Nutlin-activated p53 induces G1 and G2 arrest in cancer cell lines with wild-type p53. (A) Human cancer lines in exponential growth were treated with nutlin-3a or nutlin-3b for 24 h, and the expression of the p53 target gene p21 was measured by quantitative real-time PCR and expressed as fold increase SD. Cell-cycle profile before and after treatment with 10 µM nutlin-3a or an equivalent amount of solvent for 24 h was analyzed by BrdUrd labeling and flow cytometry. (B) Cell-cycle distribution was calculated from the flow cytograms in A and expressed as the percentage of the total population rounded to the full percentage value. Cell-cycle distribution from an independent experiment is shown in parentheses.

 

Figure 3
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Fig. 3. Apoptotic response of cancer cells with wild-type p53 to nutlin-3. Cells in exponential phase were treated with 10 µM nutlin-3a or nutlin-3b for 24 or 48 h, and the percentage of Annexin V-positive cells (live plus dead) was determined by the Guava Nexin kit and expressed as a percentage of the total cell number as in ref. 28. Data bars represent the average of two independent experiments.

 

Figure 4
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Fig. 4. Nutlin-3 stabilizes p53 and induces the p53 pathway in osteosarcoma cells. (A) Exponentially proliferating SJSA-1, MHM, and U2OS cells were treated with 10 µM nutlin-3a, nutlin-3b, or DMSO (c) for 24 h, and p53, p21, and MDM2 proteins in the cell lysates were analyzed by Western blotting. (B) Cells were treated with 10 µM nutlin-3a or nutlin-3b for the indicated times and analyzed by Western blotting. Representative results from two independent experiments are shown.

 

Figure 5
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Fig. 5. Nutlin-3-induced gene profiles differ between cells with high and low apoptotic index. (A) Nutlin-3a effectively arrests cell-cycle progression in the osteosarcoma cell lines SJSA-1, MHM, and U2OS. Cell-cycle analysis was performed as in Fig. 2. (B) Apoptosis induced by nutlin-3a in osteosarcoma cells. Treatment with nutlin-3a and determination of Annexin V-positive cell fraction was as in Fig. 3. (C) Differentially expressed genes in cells with high and low apoptotic index after 24 h incubation with 10 µM nutlin-3a. Expression profile was determined by Affymetrix gene array analysis (HG-U95 GeneChips) in cells treated with nutlin-3a or nutlin-3b. A heat map of the 62 probe sets found to be differentially expressed in SJSA-1 and MHM cells, but not in U2OS or HCT116, is shown. Differential expression was determined by a 3-fold change compared with untreated controls and an ANOVA P < 0.001 under a simple model including treatment, cell line, and their interaction. Red indicates activated genes; green indicates inhibited genes.

 

Figure 6
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Fig. 6. In vivo activity of nutlin-3a. (A) Nude mice bearing established SJSA-1 tumor xenografts received nutlin-3a for 3 weeks, and tumor growth was followed periodically. Error bars show SD from the mean volume (P < 0.01 for 200 mg/kg). (B) Nude mice with established SJSA-1 xenografts (three animals per group) received three oral doses of nutlin-3a (150 mg/kg) or vehicle and were killed 3 h after the last dose. Tumors were harvested and analyzed for the presence of the p53 targets MDM2 and p21 by Western blotting. (C) Nude mice with established tumor xenografts (100–200 mm3) were treated orally twice daily with 200 mg/kg nutlin-3a for 2 weeks (LnCaP and 22Rv1) or 3 weeks (MHM), and tumor volumes were recorded periodically. Error bars show SD from the mean volume. P was < 0.01 for all treatments.

 


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