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International Journal of Colorectal Disease

, Volume 21, Issue 3, pp 231–237 | Cite as

An increase in the number of adhesion proteins with altered expression is associated with an increased risk of cancer death for colon carcinoma patients

  • Johan Bondi
  • Geir Bukholm
  • Jahn M. Nesland
  • Arne Bakka
  • Ida R. K. BukholmEmail author
Original Article

Abstract

Background and aims

Reduced expression of components of the cell–cell adhesive cadherin–catenin complex has been related to the invasive phenotype in many malignancies, but the prognostic value of altered expression of its separate components varies in colon cancer. Our objective was evaluation of the cadherin–catenin complex, considered as a functional unit, in colon carcinomas and its relationship to patient outcome.

Patients and methods

Tumours from 206 patients operated for colon adenocarcinoma were analysed using immunohistochemistry of E-cadherin, α, β, and γ-catenins, and p120ctn. The sum of proteins with altered membranous expression was calculated as an overall adhesion score (ranging from 0 to 5) for each patient. The results were correlated with patient outcome.

Results

Of the tumours included in the analysis 0.5% had score 0, 4.9% had score 1, 13.6% had score 2, 31.6% had score 3, 33.0% had score 4, and 16.5% tumours had score 5. None of the proteins examined had individual, independent prognostic value. However, an increase in the number of proteins in the cadherin–catenin complex with altered expression was associated with an increased risk of cancer death (univariate P=0.002; multivariate P=0.007, HR 1.48, 95% CI 1.11–1.96).

Conclusions

An increase in the number of adhesion proteins with altered expression in the primary tumour is associated with increasingly impaired prognosis for patients operated for colon carcinoma. The results reveal that the entire cadherin–catenin complex should be evaluated when assessing its prognostic value in the disease.

Keywords

Adhesion proteins Immunohistochemistry Colon adenocarcinoma Prognosis 

Notes

Acknowledgements

The excellent technical assistance of Grethe Berg Pedersen, Sølvi Westre and Ellen Hellesylt is gratefully acknowledged.

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Copyright information

© Springer-Verlag 2005

Authors and Affiliations

  • Johan Bondi
    • 1
    • 2
    • 3
  • Geir Bukholm
    • 2
    • 3
  • Jahn M. Nesland
    • 3
    • 4
  • Arne Bakka
    • 1
    • 3
  • Ida R. K. Bukholm
    • 1
    • 3
    Email author
  1. 1.Department of SurgeryAkershus University HospitalNordbyhagenNorway
  2. 2.Institute of Clinical Epidemiology and Molecular BiologyAkershus University HospitalAkershusNorway
  3. 3.University of OsloOsloNorway
  4. 4.Department of PathologyThe Norwegian Radium HospitalOsloNorway

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