Clinical significance of Keap1 and Nrf2 in oral squamous cell carcinoma

PLoS One. 2013 Dec 27;8(12):e83479. doi: 10.1371/journal.pone.0083479. eCollection 2013.

Abstract

Oxidative stress has been reported to play an important role in progression and prognostication in various kinds of cancers. However, the role and clinical significance of oxidative stress markers Keap1 and Nrf2 in oral squamous cell carcinoma (OSCC) has not been elucidated. This study aimed to investigate the correlation of oxidative stress markers Keap1 and Nrf2 expression and pathological features in OSCC by using tissue microarray. Tissue microarrays containing 17 normal oral mucosa, 7 oral epithelial dysplasia and 43 OSCC specimens were studied by immunohistochemistry. The association among these proteins and pathological features were analyzed. Expression of oxidative stress markers Keap1, Nrf2, and antioxidants PPIA, Prdx6, as well as CD147 was found to increase consecutively from normal oral mucosa to OSCC, and the Keap1, Nrf2, PPIA, Prdx6, CD147 expression in OSCC were significantly higher when compared to normal oral mucosa. Expression of Keap1, Nrf2 in tumors was not found to be significantly associated with T category, lymph node metastases, and pathological grade. Furthermore, we checked the relationship among these oxidative stress markers and found that Keap1 was significantly correlated with Nrf2, Prdx6 and CD147. Significant relationship between Nrf2 and Prdx6 was also detected. Finally, we found patients with overexpression of Keap1 and Nrf2 had not significantly worse overall survival by Kaplan-Meier analysis. These findings suggest that ROS markers are associated with carcinogenesis and progression of OSCC, which may have prognostic value and could be regarded as potential therapeutic targets in OSCC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basigin / genetics
  • Basigin / metabolism
  • Biomarkers, Tumor / metabolism
  • Carcinoma, Squamous Cell / genetics
  • Carcinoma, Squamous Cell / metabolism*
  • Carcinoma, Squamous Cell / pathology*
  • Cluster Analysis
  • Cyclophilin A / genetics
  • Cyclophilin A / metabolism
  • Gene Expression Profiling
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Kelch-Like ECH-Associated Protein 1
  • Lymphatic Metastasis
  • Mouth Neoplasms / genetics
  • Mouth Neoplasms / metabolism*
  • Mouth Neoplasms / pathology*
  • NF-E2-Related Factor 2 / genetics
  • NF-E2-Related Factor 2 / metabolism*
  • Neoplasm Grading
  • Neoplasm Staging
  • Patient Outcome Assessment
  • Peroxiredoxin VI / genetics
  • Peroxiredoxin VI / metabolism
  • Prognosis

Substances

  • Biomarkers, Tumor
  • Intracellular Signaling Peptides and Proteins
  • KEAP1 protein, human
  • Kelch-Like ECH-Associated Protein 1
  • NF-E2-Related Factor 2
  • Basigin
  • PRDX6 protein, human
  • Peroxiredoxin VI
  • Cyclophilin A

Grants and funding

This work was supported by National Natural Science Foundation of China 81072203, 81272963 (ZJS). 81272964 (WFZ), 81371106 (LZ), 81371159 (YFZ). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.