[Expression of DOG-1 in gastrointestinal stromal tumors and its significance]

Zhonghua Wei Chang Wai Ke Za Zhi. 2013 Mar;16(3):256-9.
[Article in Chinese]

Abstract

Objective: To identify the expression of DOG-1 in gastrointestinal stromal tumors (GIST) and to explore its potential association with clinicopathological features of GIST.

Methods: Two tissue microarrays (TMA) were used for the study. Each TMA contained 80 tissue samples of GIST from 80 different patients, with each tumor represented by one core, and paraffin-embedded sections of 40 samples from normal gastrointestinal tissue were used as control. Immunohistochemistry staining (SABC method) was performed on TMA and paraffin-embedded sections to detected the expression of c-Kit (CD117) and DOG-1.

Results: Immunohistochemistry showed that in 80 GIST patients, 76 cases (95.0%) were DOG-1 positive and 67 cases (83.8%) were CD117 positive. The positive rate of DOG-1 was higher than that of CD117 (P<0.05). In 13 GIST samples of negative CD117, the positive rate of DOG-1 was 100%. Expressions of both DOG-1 and CD117 were negative in all the 40 samples of normal gastrointestinal tissue. The positive expression of DOG-1 and CD117 was not significantly different in spindle cell type (96.0% vs. 96.0%, P>0.05) and in mixed cell type (91.7% vs. 75.0%, P>0.05). While in the epithelioid cell type, the DOG-1 expression was higher than CD117 expression (94.1% vs. 52.9%, P<0.05). The positive expression of DOG-1 and CD117 was not associated with age, gender, location and risk stratification of the tumors (all P>0.05).

Conclusions: DOG-1 expression is up-regulated in gastrointestinal stromal tumors, especially in epithelioid cell GIST, and may be used as a new marker in the diagnosis of GIST.

MeSH terms

  • Adult
  • Aged
  • Anoctamin-1
  • Biomarkers, Tumor / metabolism
  • Chloride Channels / metabolism*
  • Female
  • Gastrointestinal Neoplasms / metabolism*
  • Gastrointestinal Stromal Tumors / metabolism*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Proteins / metabolism*
  • Young Adult

Substances

  • ANO1 protein, human
  • Anoctamin-1
  • Biomarkers, Tumor
  • Chloride Channels
  • Neoplasm Proteins