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J Clin Pathol 2007;60:608-614 doi:10.1136/jcp.2005.031443
  • Original article

Differential expression and distribution of epithelial adhesion molecules in non-small cell lung cancer and normal bronchus

  1. M C Boelens1,
  2. A van den Berg1,
  3. I Vogelzang1,
  4. J Wesseling1,
  5. D S Postma2,
  6. W Timens1,
  7. H J M Groen2
  1. 1Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
  2. 2Department of Pulmonology, University Medical Center Groningen
  1. Correspondence to:
 M C Boelens
 Department of Pathology and Laboratory Medicine, University Medical Center Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands;m.c.boelens{at}path.umcg.nl
  • Accepted 28 September 2005
  • Published Online First 17 February 2006

Abstract

Background: Changes in epithelial cell interactions have been implicated in carcinogenesis, tumour invasion and metastasis.

Aim: To screen for altered expression of epithelial adhesion genes in lung cancer development.

Methods: Gene expression profiles were assessed with cDNA expression arrays in eight non-small cell lung cancer (NSCLC) and eight normal bronchi obtained from the same patient. Immunohistochemistry (IHC) and RNA in situ hybridisation (ISH) were used to confirm the most prominently expressed adhesion molecules and to investigate their distribution at protein and mRNA levels.

Results: 43 differentially expressed cancer-related genes were identified in adenocarcinoma, squamous cell carcinoma (SCC) and normal bronchus. Five of these genes are related to epithelial adhesion—that is, integrin α3 (ITGA3), integrin β4 (ITGB4), desmoplakin I and II (DSP), plakoglobin, and desmocollin 3 (DSC3). ITGA3 and ITGB4, showing predominantly cell–matrix staining, were up regulated in adenocarcinoma and SCC, respectively. ITGB4 also showed strong staining in SCC with IHC and ISH. Components of the desmosome adhesion complex DSP, plakoglobin and DSC3 were strongly up regulated in SCC and showed a distinct cell–cell staining pattern. DSP and plakoglobin were predominantly present at central, more differentiated tumour cells, whereas DSC3 showed a stronger staining in the peripheral basal cells of SCC tumour areas.

Conclusions: Lack of cellular adhesion may have an important role in the metastatic potency of a primary tumour. A possible association of strong presence and normal-distributed desmosomal molecules in SCC with the less frequent and late pattern of metastasis in SCC as compared with adenocarcinoma is suggested.

Footnotes

  • Published Online First 17 February 2006

  • Competing interests: None declared.

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