Skip to content
2000
Volume 22, Issue 16
  • ISSN: 1381-6128
  • E-ISSN: 1873-4286

Abstract

Multiple pathogenic mechanisms contribute to the development of colorectal cancer. This tumor is characterized by high chemoresistance and low immunogenicity due to the effective mechanisms of immunosuppression. Dendritic cells (DCs) play a key role in recognition of tumor antigens and induction of T-cell-primed anticancer response. However, in cancer microenvironment, the function of tumor-infiltrating DCs becomes impaired and switched from the immunostimulation to the immunosuppression. Colorectal cancer cells express anti-inflammatory cytokines such as IL-10 and TGF-β that could affect DC phenotype and support tumor escape from the immune surveillance. As a result, tumor-associated DCs display numerous defects in antigen-presenting capacity and have an altered pattern of expression of immune costimulatory molecules towards the immunoregulatory phenotype. Indeed, understanding of mechanisms, such as how tumor could impair activity of DCs, would help in the development of new DC-based vaccines against colorectal cancer.

Loading

Article metrics loading...

/content/journals/cpd/10.2174/1381612822666160203141740
2016-05-01
2025-04-04
Loading full text...

Full text loading...

/content/journals/cpd/10.2174/1381612822666160203141740
Loading

  • Article Type:
    Research Article
Keyword(s): Colorectal cancer; dendritic cells; immune reactions; therapeutic approaches
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test