High DcR3 expression predicts stage pN2 in gastric cancer

Hepatogastroenterology. 2007 Oct-Nov;54(79):2172-6.

Abstract

Background/aims: A soluble decoy receptor 3 (DcR3), also known as TR6 or M68, is a member of the TNF receptor family. It has been reported that high DcR3 expression occurs in many tumors.

Methodology: This prospective study evaluated the DcR3 tissue status by RT-PCR and its correlation with the lymph node (N) stages in 62 primary gastric cancers.

Results: DcR3 expression levels in patients with pN2 disease were much higher than those in patients with pN0-1 disease (Median values 1.31 vs. 0, P< 0.01). Using ROC analysis, a cut-off level of DcR3 expression at 1.20 was found to be associated with optimal sensitivity and specificity of 62.5% (15/24) and 92.1% (35/38) respectively, in the prediction of stage pN2. According to the cut-off value, patients were divided into two groups with relatively high and low levels of DcR3 expression. Among the 18 patients with high DcR3 expression, 83.3% (15/18) showed metastases to the second level lymph nodes. In the other 44 patients with low DcR3 expression, only 20.5% (9/44) had secondary nodal involvement. Logistic regression analysis for stage pN2 revealed that high DcR3 expression was an independent risk factor.

Conclusions: Gastric cancer patients with high DcR3 expression presented more advanced pN2 disease than those with low DcR3 expression. Preoperative checking DcR3 expression might be an additional approach to imaging modalities for evaluating N stages in gastric cancer to guide the operative procedures.

Publication types

  • Duplicate Publication
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / metabolism*
  • Adenocarcinoma / pathology*
  • Aged
  • Aged, 80 and over
  • Female
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Neoplasm Invasiveness
  • Neoplasm Staging
  • Predictive Value of Tests
  • Prospective Studies
  • ROC Curve
  • Receptors, Tumor Necrosis Factor, Member 6b / metabolism*
  • Sensitivity and Specificity
  • Stomach Neoplasms / metabolism*
  • Stomach Neoplasms / pathology*

Substances

  • Receptors, Tumor Necrosis Factor, Member 6b
  • TNFRSF6B protein, human