Expression of Nogo isoforms and Nogo-B receptor (NgBR) in non-small cell lung carcinomas

Anticancer Res. 2014 Aug;34(8):4059-68.

Abstract

Background: Nogo-B was recently shown to be involved in proliferation, apoptosis and invasiveness of cancer cells, whereas its specific receptor (NgBR) was found to be up-regulated in estrogen receptor-α positive breast cancer. No data are currently available concerning their expression in non-small cell lung carcinomas (NSCLC).

Materials and methods: Expression of Nogo isoforms and NgBR was studied in 191 NSCLC.

Results: Higher Nogo-A/B immunoreactivity was noted in cancer cells of squamous cell carcinomas (SQC) compared to adenocarcinomas (p<0.001). Stage II-IV tumors had the lowest Nogo-A/B expression (p<0.0001) compared to stage I cases. Nogo-A/B expression decreased with increasing SQC malignancy grade (p=0.026). Significant NgBR mRNA down-regulation was associated with larger primary tumor size (p=0.039), lymph node involvement (p=0.039) and advancement stage (p=0.0054). Low NgBR mRNA expression predicted poor patients outcome (p=0.029).

Conclusion: The current data may point to the involvement of Nogo isoforms and NgBR in the pathogenesis of NSCLC.

Keywords: Nogo; Nogo-B receptor; Non-small cell lung carcinoma; immunohistochemistry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma, Non-Small-Cell Lung / chemistry*
  • Carcinoma, Non-Small-Cell Lung / etiology
  • Carcinoma, Non-Small-Cell Lung / mortality
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Female
  • Humans
  • Immunohistochemistry
  • Lung Neoplasms / chemistry*
  • Lung Neoplasms / etiology
  • Lung Neoplasms / mortality
  • Lung Neoplasms / pathology
  • Male
  • Middle Aged
  • Myelin Proteins / analysis
  • Myelin Proteins / genetics
  • Myelin Proteins / physiology*
  • Neoplasm Staging
  • Nogo Proteins
  • Protein Isoforms / analysis
  • Protein Isoforms / genetics
  • Protein Isoforms / physiology
  • RNA, Messenger / analysis
  • Receptors, Cell Surface / analysis
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / physiology*

Substances

  • Myelin Proteins
  • NUS1 protein, human
  • Nogo Proteins
  • Protein Isoforms
  • RNA, Messenger
  • RTN4 protein, human
  • Receptors, Cell Surface