A simple immunohistochemical algorithm predicts the risk of distant metastases in right-sided colon cancer

Histopathology. 2012 Feb;60(3):416-26. doi: 10.1111/j.1365-2559.2011.04126.x.

Abstract

Aims: A test predicting distant metastases would be valuable for prognostication in colon cancer (CC). In previous studies, CC with microsatellite instability (MSI) showed a reduced risk of distant metastases. High expression of CD133 and β-catenin, both related to cancer stem cell phenotypes, might be predictive markers for metastasis. The aim of this study was to develop a simple and robust test for risk assessment of distant metastases in CC.

Methods and results: In a case-control study, 57 cases of right-sided CC specimens with synchronous distant metastases were matched with 57 CC without distant metastases. Immunohistochemistry for MLH1, CD133 and nuclear β-catenin was carried out. To define the diagnostic algorithm the tumours were first stratified according to their MLH1 expression. Loss of MLH1 expression was correlated significantly with a very low risk of distant metastases (5.3%; P = 0.00003). In MLH1-positive cases, combined high scores of CD133 and β-catenin were associated with a very high rate of distant metastases (94.4%), whereas the risk was intermediate for carcinomas with either low CD133 and/or low β-catenin expression (P = 0.0007). A validation study using an independent set of 68 right-sided CC specimens showed a clear trend towards risk stratification according to the algorithm; however, sample sizes were small, and associations were not statistically significant.

Conclusions: By the use of three markers, this algorithm allowed identification of subgroups of right-sided CC patients with extremely high and extremely low risk of distant metastases.

Publication types

  • Validation Study

MeSH terms

  • AC133 Antigen
  • Adaptor Proteins, Signal Transducing / metabolism
  • Adenocarcinoma / diagnosis*
  • Adenocarcinoma / genetics
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / secondary
  • Aged
  • Algorithms*
  • Antigens, CD / metabolism
  • Biomarkers, Tumor / metabolism
  • Case-Control Studies
  • Cell Nucleus / metabolism
  • Cell Nucleus / pathology
  • Colonic Neoplasms / diagnosis*
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / metabolism
  • Female
  • Glycoproteins / metabolism
  • Humans
  • Immunohistochemistry / methods*
  • Male
  • Microsatellite Instability
  • MutL Protein Homolog 1
  • Neoplasm Grading
  • Neoplasm Metastasis / diagnosis
  • Neoplasm Metastasis / genetics
  • Nuclear Proteins / metabolism
  • Peptides / metabolism
  • Predictive Value of Tests
  • Prognosis
  • Proto-Oncogene Proteins B-raf / genetics
  • Proto-Oncogene Proteins B-raf / metabolism
  • Risk Assessment
  • beta Catenin / metabolism

Substances

  • AC133 Antigen
  • Adaptor Proteins, Signal Transducing
  • Antigens, CD
  • Biomarkers, Tumor
  • CTNNB1 protein, human
  • Glycoproteins
  • MLH1 protein, human
  • Nuclear Proteins
  • PROM1 protein, human
  • Peptides
  • beta Catenin
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • MutL Protein Homolog 1