Abstract

BackgroundCodon 72 (Arg/Pro), the most frequently studied single nucleotide polymorphism (SNP) of p53 to date, is associated with the ability of the gene to induce cell apoptosis. The PI3K/Akt pathway plays an essential role in the transcriptional activation function of p53, and is an important factor in radiotherapy resistance. The present study was designed to evaluate the prediction of response to radiotherapy based on p53 codon 72 SNP and pAkt expression in biopsy specimens of locoregional nasopharyngeal carcinoma (NPC) before treatment.Materials and methodsIn total, 75 consecutive patients with locoregional NPC were enrolled. The p53 codon 72 SNP was identified from retrospectively collected paraffin-embedded biopsy specimens using Sanger sequencing. Expression patterns of p53, p21, 14-3-3σ, and pAkt proteins were investigated using immunohistochemical analyses. The effects of genetic polymorphisms and protein expression on progression-free survival (PFS) were evaluated using the Cox proportional hazards model, Kaplan–Meier method, and log-rank test.ResultsThe p53 codon 72 Pro/Pro carriers showed lower risk of disease progression (local recurrence and distant metastases) (HR: 0.300; 95% CI: 0.092–0.983; p=0.047). However, this association between the p53 codon 72 polymorphism and PFS was not significant in the pAkt-positive subgroup. No association was observed between protein expression of p53, p21 or 14-3-3σ and p53 codon72 polymorphisms. Notably, positive expression of p53 protein appeared to be correlated with poorer PFS among patients diagnosed as local regional lymph node metastasis (N+) before treatment (p=0.032).ConclusionsThe p53 codon 72 Pro/Pro genotype may be an effective independent prognostic marker for better outcome in patients with locoregional NPC. Based on the current findings, we hypothesize that pAkt weakens the predictive value of p53 codon 72 SNP in NPC. A combination of positive p53 protein expression and local regional lymph node metastasis may additionally be predictive of high risk of disease progression.

Highlights

  • Nasopharyngeal carcinoma (NPC) is an epithelial malignancy with an annual incidence of 15 to 50 cases per 100,000 individuals in Southern China [1]

  • Based on the current findings, we hypothesize that pAkt weakens the predictive value of p53 codon 72 single nucleotide polymorphism (SNP) in nasopharyngeal carcinoma (NPC)

  • Our results suggest that the p53 codon72 Pro/Pro genotype is associated with improved progression-free survival (PFS) in locoregional NPC patients

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Summary

Introduction

Nasopharyngeal carcinoma (NPC) is an epithelial malignancy with an annual incidence of 15 to 50 cases per 100,000 individuals in Southern China [1]. The prognosis of patients with NPC in the early stages is generally favorable, the incidence of relapse remains high domains. This proline-rich region has been shown to be critical for p53 function, its ability to induce apoptosis. Vannini et al [13] reported a significantly shorter time of disease progression and overall survival in metastatic breast cancer patients homozygous for Arg, compared to those with heterozygous Arg/Pro tumors. The present study was designed to evaluate the prediction of response to radiotherapy based on p53 codon 72 SNP and pAkt expression in biopsy specimens of locoregional nasopharyngeal carcinoma (NPC) before treatment

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