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Article

A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats

  • Authors:
    • Nengtai Ouyang
    • Ping Ji
    • Jennie L. Williams
  • View Affiliations / Copyright

    Affiliations: Division of Cancer Prevention, Department of Medicine, Stony Brook University, Stony Brook, NY 11794-8175, USA
  • Pages: 643-650
    |
    Published online on: December 28, 2012
       https://doi.org/10.3892/ijo.2012.1756
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Abstract

The cancer chemopreventive properties and gastrointestinal toxicity of ibuprofen are well documented. Modification of existing NSAIDs has improved on the chemopreventive efficacy of this agent and reduced its toxicity. In this study, ibuprofen and a modified derivative (phospho-modified ibuprofen or p-ibuprofen) were used in a chemically induced model of colon cancer. Fisher 344 rats were injected with azoxymethane then treated with either ibuprofen (500 ppm) or p-ibuprofen (900 ppm) for 20 weeks to observe aberrant crypt foci (ACF) or 40 weeks to evaluate tumor incidence and multiplicity. β-catenin and p65 were measured in colonic tissues by immunofluorescence staining. Equal molar doses of ibuprofen (75 and 670 mg/kg) and p-ibuprofen (135 and 1,215 mg/kg) were administered to rats for 7 days to assess acute toxicity. The in vitro effect of p-ibuprofen on COX-2 and PGE2 synthesis, β-catenin expression and NF-κB activity were examined in RAW 264.7 macrophage and HCT 116 colon cancer cells. At week 20, p-ibuprofen and ibuprofen significantly reduced the multiplicity of ACF compared with control (p<0.05); 31.2 and 37.9%, respectively. At week 40, p-ibuprofen and ibuprofen reduced the multiplicity of colon tumors compared with control (p<0.01) by 47.2 and 56.6%, respectively. Equal molar concentrations of ibuprofen (670 mg/kg) and p-ibuprofen (1,215 mg/kg) resulted in stomach ulceration in 85.7% (6 out of 7) and 14.3% (1 out of 7) of rats, respectively, with p<0.01. Immunofluoresence staining and western blot analysis demonstrated that both ibuprofen and p-ibuprofen suppressed β-catenin nuclear translocation in colon cancer cells. In addition, p-ibuprofen but not ibuprofen inhibited NF-κB activation in colon cancer cells. Collectively, these results suggest that p-ibuprofen is a potential effective novel drug for long-term use in colon cancer prevention.
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Copy and paste a formatted citation
Spandidos Publications style
Ouyang N, Ji P and Williams JL: A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats. Int J Oncol 42: 643-650, 2013.
APA
Ouyang, N., Ji, P., & Williams, J.L. (2013). A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats. International Journal of Oncology, 42, 643-650. https://doi.org/10.3892/ijo.2012.1756
MLA
Ouyang, N., Ji, P., Williams, J. L."A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats". International Journal of Oncology 42.2 (2013): 643-650.
Chicago
Ouyang, N., Ji, P., Williams, J. L."A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats". International Journal of Oncology 42, no. 2 (2013): 643-650. https://doi.org/10.3892/ijo.2012.1756
Copy and paste a formatted citation
x
Spandidos Publications style
Ouyang N, Ji P and Williams JL: A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats. Int J Oncol 42: 643-650, 2013.
APA
Ouyang, N., Ji, P., & Williams, J.L. (2013). A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats. International Journal of Oncology, 42, 643-650. https://doi.org/10.3892/ijo.2012.1756
MLA
Ouyang, N., Ji, P., Williams, J. L."A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats". International Journal of Oncology 42.2 (2013): 643-650.
Chicago
Ouyang, N., Ji, P., Williams, J. L."A novel NSAID derivative, phospho-ibuprofen, prevents AOM-induced colon cancer in rats". International Journal of Oncology 42, no. 2 (2013): 643-650. https://doi.org/10.3892/ijo.2012.1756
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