TAP1 down-regulation elicits immune escape and poor prognosis in colorectal cancer

Agnes Ling1, Anna Löfgren-Burström1, Pär Larsson1

  • 1Department of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.

Oncoimmunology
|November 18, 2017
PubMed

Insights

Downregulated TAP1 expression in colorectal cancer (CRC) indicates poor prognosis and reduced immune cell infiltration. This suggests TAP1 downregulation is a general immune escape mechanism in CRC, potentially linked to gene methylation.

Area of Science:

  • Immunology
  • Oncology
  • Molecular Biology

Background:

  • The anti-tumor immune response and tumor immune evasion are critical prognostic factors in colorectal cancer (CRC).
  • Understanding tumor factors influencing immunity is essential for developing effective cancer therapies.

Purpose of the Study:

  • To investigate tumor factors contributing to immune escape in colorectal cancer (CRC).
  • To identify potential mechanisms of tumor immune evasion using gene expression analysis.

Main Methods:

  • Gene expression array analysis to identify candidate genes involved in immune escape.
  • Immunohistochemistry to evaluate TAP1 protein expression in 436 CRC patients.
  • Correlation analysis of TAP1 expression with immune cell infiltration, molecular characteristics, methylation, and patient prognosis.

Main Results:

  • Downregulated TAP1 expression was significantly associated with reduced infiltration of lymphocytes and macrophages.
  • TAP1 downregulation was independent of molecular characteristics, indicating a broad mechanism beyond MSI CRCs.
  • Low TAP1 expression correlated with poor prognosis in CRC patients, particularly in early-stage (I-II) tumors.
  • TAP1 expression showed an inverse correlation with promoter region methylation.

Conclusions:

  • Downregulation of TAP1 represents a general mechanism of tumor immune escape in colorectal cancer (CRC).
  • Reduced TAP1 expression is a significant negative prognostic factor for early-stage CRC patients.
  • Gene methylation is a potential mechanism driving TAP1 downregulation in CRC.