Identification of epidermal growth factor receptor (EGFR) exon 20 single nucleotide polymorphism in Chinese squamous cell carcinoma of head and neck (SCCHN)

Acta Otolaryngol. 2009 Nov;129(11):1306-12. doi: 10.3109/00016480802620662.

Abstract

Conclusion: The 78th single nucleotide polymorphism (SNP) in exon 20 of epidermal growth factor receptor (EGFR) might be a predictor of the clinical course of squamous cell carcinoma of the head and neck (SCCHN), and genetic predisposition could influence the progression of SCCHN in Chinese subjects.

Objective: To analyze the clinical significance of EGFR SNP in Chinese SCCHN patients.

Materials and methods: Direct sequencing of exons 18-21 was used to analyze somatic mutations of EGFR. Reverse transcriptase polymerase chain reaction (RT-PCR) was used to evaluate the expression level of EGFR. The chi-square test and Kaplan-Meier method were the main statistical methods used to analyze the correlation of the investigated variables and prognostic significance.

Results: In analyzing exons 18-21 of EGFR in 96 patients with SCCHN, only one SNP was found in the 78th site of exon 20 and it mostly existed in specimens coming from the hypopharynx. Further statistical analysis showed that among the clinical or histopathologic parameters, the 78th SNP had a close relationship with earlier stage and more localized primary carcinoma, while at present the analysis did not support the proposition that the SNP was an independent prognostic factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / mortality
  • Carcinoma, Squamous Cell / pathology
  • China
  • Disease-Free Survival
  • ErbB Receptors / genetics*
  • Exons / genetics*
  • Female
  • Gene Expression Regulation, Neoplastic / physiology
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Hypopharyngeal Neoplasms / genetics
  • Hypopharyngeal Neoplasms / pathology
  • Male
  • Middle Aged
  • Neoplasm Staging
  • Otorhinolaryngologic Neoplasms / genetics*
  • Otorhinolaryngologic Neoplasms / mortality
  • Otorhinolaryngologic Neoplasms / pathology
  • Polymorphism, Single Nucleotide / genetics*
  • Prognosis
  • Protein-Tyrosine Kinases / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • EGFR protein, human
  • ErbB Receptors
  • Protein-Tyrosine Kinases