Low expression of chemokine receptor CCR5 in human colorectal cancer correlates with lymphatic dissemination and reduced CD8+ T-cell infiltration

Int J Colorectal Dis. 2010 Apr;25(4):417-24. doi: 10.1007/s00384-009-0868-y.

Abstract

Background: Chemokines and their receptors have been proposed to distinctly contribute to tumor growth, dissemination, and local immune escape. The aim of this study was to evaluate the relevance of the chemokine receptor CCR5 expression for the progression of human colorectal cancer.

Methods: CCR5 expression was assessed by RT-PCR analysis in 103 colorectal cancer patients. Intensity of CCR5 expression was correlated with both tumor and patient characteristics. Infiltration of tumor margins with CD8(+) T cells in the context of CCR5 expression was analyzed by immunohistochemistry in additional 18 colorectal cancer specimens.

Results: Human colorectal cancer revealed variable intensities of CCR5 expression ranging from absent (48/103: 47%), weak (30/103: 29%), intermediate (13/103: 13%), to strong (12/103: 12%). Absent or weak CCR5 expression was significantly associated with advanced UICC stages (P=0.02) and lymphatic metastasis (P=0.05). In addition, CCR5 expression positively correlated with CD8(+) T-cell infiltration in tumor margins (P=0.001).

Conclusion: In summary, intermediate and strong CCR5 expression was significantly associated with nonmetastatic colorectal cancer and increased CD8(+) T-cell infiltration.

MeSH terms

  • Biomarkers
  • Biomarkers, Tumor
  • CD8-Positive T-Lymphocytes / immunology*
  • Chemotaxis, Leukocyte / immunology
  • Colorectal Neoplasms / immunology*
  • Colorectal Neoplasms / pathology
  • Gene Expression Regulation, Neoplastic / immunology*
  • Humans
  • Immunohistochemistry
  • Lymphatic Metastasis / diagnosis
  • Lymphatic Metastasis / immunology*
  • Neoplasm Staging / methods
  • Receptors, CCR5 / analysis
  • Receptors, CCR5 / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Biomarkers
  • Biomarkers, Tumor
  • Receptors, CCR5