4.3 Article

The prognostic role of tissue TLR2 and TLR4 in colorectal cancer

期刊

VIRCHOWS ARCHIV
卷 477, 期 5, 页码 705-715

出版社

SPRINGER
DOI: 10.1007/s00428-020-02833-5

关键词

Toll-like receptor 2; Toll-like receptor 4; Colorectal cancer; Colon cancer; Immunohistochemistry

资金

  1. University of Helsinki
  2. Helsinki University Central Hospital
  3. Competitive State Research Financing of the Expert Responsibility Area of Helsinki University Hospital
  4. Kurt och Doris Palander Foundation
  5. Finnish Cancer Foundation
  6. Finska Lakaresallskapet
  7. K. Albin Johansson Foundation
  8. Sigrid Juselius Foundation

向作者/读者索取更多资源

Colorectal cancer (CRC), the second most common cancer globally, resulted in 881,000 deaths in 2018. Toll-like receptors (TLRs) are crucial to detecting pathogen invasion and inducing the host's immune response. This study aimed to explore the prognostic value of TLR2 and TLR4 tumor expressions in colorectal cancer patients. We studied the immunohistochemical expressions of TLR2 and TLR4 using tissue microarray specimens from 825 patients undergoing surgery in the Department of Surgery, Helsinki University Hospital, between 1982 and 2002. We assessed the relationships between TLR2 and TLR4 expressions and clinicopathological variables and patient survival. We generated survival curves using the Kaplan-Meier method, determining significance with the log-rank test. Among patients with lymph node-positive disease and no distant metastases (Dukes C), a strong TLR2 immunoactivity associated with a better prognosis (p < 0.001). Among patients with local Dukes B disease, a strong TLR4 immunoactivity associated with a worse disease-specific survival (DSS; p = 0.017). In the multivariate survival analysis, moderate TLR4 immunoactivity compared with strong TLR4 immunoactivity (hazard ratio (HR) 0.66, 95% confidence interval (CI) 0.49-0.89, p = 0.007) served as an independent prognostic factor. In the multivariate analysis for the Dukes subgroups, moderate TLR2 immunoactivity (HR 2.63, 95% CI 1.56-4.44, p < 0.001) compared with strong TLR2 immunoactivity served as an independent negative prognostic factor in the Dukes C subgroup. TLR2 and TLR4 might be new prognostic factors to indicate which CRC patients require adjuvant therapy and which could spare from an unnecessary follow-up, but further investigations are needed.

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