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Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity

  • Authors:
    • Yee-Lin Voon
    • Munirah Ahmad
    • Pooi-Fong Wong
    • Roslina Husaini
    • Wayne Tiong-Weng Ng
    • Chee-Onn Leong
    • David Philip Lane
    • Alan Soo-Beng Khoo
  • View Affiliations / Copyright

    Affiliations: Molecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, Kuala Lumpur 50588, Malaysia, Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia, School of Pharmacy and Health Sciences, International Medical University, Kuala Lumpur 57000, Malaysia, p53 Laboratory (p53Lab), Agency for Science, Technology and Research (A*STAR), 8A Biomedical Grove, Immunos, Singapore 138648, Republic of Singapore
    Copyright: © Voon et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 1692-1700
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    Published online on: August 5, 2015
       https://doi.org/10.3892/or.2015.4177
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Abstract

The small-molecule inhibitor of p53-Mdm2 interaction, Nutlin-3, is known to be effective against cancers expressing wild-type (wt) p53. p53 mutations are rare in nasopharyngeal carcinoma (NPC), hence targeting disruption of p53-Mdm2 interaction to reactivate p53 may offer a promising therapeutic strategy for NPC. In the present study, the effects of Nutlin-3 alone or in combination with cisplatin, a standard chemotherapeutic agent, were tested on C666-1 cells, an Epstein-Barr virus (EBV)-positive NPC cell line bearing wt p53. Treatment with Nutlin-3 activated the p53 pathway and sensitized NPC cells to the cytotoxic effects of cisplatin. The combined treatment also markedly suppressed soft agar colony growth formation and increased apoptosis of NPC cells. The effect of Nutlin-3 on NPC cells was inhibited by knockdown of p53, suggesting that its effect was p53-dependent. Extended treatment with increasing concentrations of Nutlin-3 did not result in emergence of p53 mutations in the C666-1 cells. Collectively, the present study revealed supportive evidence of the effectiveness of combining cisplatin and Nutlin-3 as a potential therapy against NPC.
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Copy and paste a formatted citation
Spandidos Publications style
Voon Y, Ahmad M, Wong P, Husaini R, Ng WT, Leong C, Lane DP and Khoo AS: Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity. Oncol Rep 34: 1692-1700, 2015.
APA
Voon, Y., Ahmad, M., Wong, P., Husaini, R., Ng, W.T., Leong, C. ... Khoo, A.S. (2015). Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity. Oncology Reports, 34, 1692-1700. https://doi.org/10.3892/or.2015.4177
MLA
Voon, Y., Ahmad, M., Wong, P., Husaini, R., Ng, W. T., Leong, C., Lane, D. P., Khoo, A. S."Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity". Oncology Reports 34.4 (2015): 1692-1700.
Chicago
Voon, Y., Ahmad, M., Wong, P., Husaini, R., Ng, W. T., Leong, C., Lane, D. P., Khoo, A. S."Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity". Oncology Reports 34, no. 4 (2015): 1692-1700. https://doi.org/10.3892/or.2015.4177
Copy and paste a formatted citation
x
Spandidos Publications style
Voon Y, Ahmad M, Wong P, Husaini R, Ng WT, Leong C, Lane DP and Khoo AS: Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity. Oncol Rep 34: 1692-1700, 2015.
APA
Voon, Y., Ahmad, M., Wong, P., Husaini, R., Ng, W.T., Leong, C. ... Khoo, A.S. (2015). Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity. Oncology Reports, 34, 1692-1700. https://doi.org/10.3892/or.2015.4177
MLA
Voon, Y., Ahmad, M., Wong, P., Husaini, R., Ng, W. T., Leong, C., Lane, D. P., Khoo, A. S."Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity". Oncology Reports 34.4 (2015): 1692-1700.
Chicago
Voon, Y., Ahmad, M., Wong, P., Husaini, R., Ng, W. T., Leong, C., Lane, D. P., Khoo, A. S."Nutlin-3 sensitizes nasopharyngeal carcinoma cells to cisplatin-induced cytotoxicity". Oncology Reports 34, no. 4 (2015): 1692-1700. https://doi.org/10.3892/or.2015.4177
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