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Immunohistochemical prognostic factors in resected colorectal lung metastases using tissue microarray analysis.

AbstractAIMS:
Immunohistochemical prognostic factors of pulmonary metastatic colorectal cancer lesions have not been well investigated. The study was conducted to identify the immunohistochemical prognostic factors of metastasized colorectal cancer.
METHODS:
We immunohistochemically investigated the expression of insulin-like growth factor-1 receptor (IGF1-R), E-cadherin, beta-catenin, and p53 using a tissue microarray in the surgical specimens of 86 metastatic lesions.
RESULTS:
The univariate analysis revealed E-cadherin and membrane beta-catenin positive to be prognostic factors. IGF1-R and p53 were not significantly associated with the patient's survival. In multivariate analysis, the reduced expression of E-cadherin, aerogenous spread with floating cancer cell clusters and vascular invasion were independent prognostic factors.
CONCLUSIONS:
The reduced expression of E-cadherin in the pulmonary metastatic lesions was an independent predictor of poor survival after pulmonary metastasectomy.
AuthorsS Shiono, G Ishii, K Nagai, Y Murata, K Tsuta, J Nitadori, T Kodama, A Ochiai
JournalEuropean journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology (Eur J Surg Oncol) Vol. 32 Issue 3 Pg. 308-9 (Apr 2006) ISSN: 0748-7983 [Print] England
PMID16459049 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Biomarkers, Tumor
  • Cadherins
  • Tumor Suppressor Protein p53
  • beta Catenin
  • Receptor, IGF Type 1
Topics
  • Biomarkers, Tumor (metabolism)
  • Cadherins (metabolism)
  • Carcinoma (metabolism, secondary, surgery)
  • Colorectal Neoplasms (metabolism, pathology)
  • Humans
  • Immunohistochemistry
  • Lung Neoplasms (metabolism, secondary, surgery)
  • Pneumonectomy
  • Prognosis
  • Receptor, IGF Type 1 (metabolism)
  • Retrospective Studies
  • Tumor Suppressor Protein p53 (metabolism)
  • beta Catenin (metabolism)

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