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Evaluation of Slug expression is useful for predicting lymph node metastasis and survival in patients with gastric cancer

Authors :
Cho Hyun Park
Jae Myung Park
Kyo Young Song
Sae Jung Na
Sung Hak Lee
Eun Sun Jung
Myung-Gyu Choi
Han Hee Lee
Joo Hyun O
Source :
BMC Cancer, BMC Cancer, Vol 17, Iss 1, Pp 1-9 (2017)
Publication Year :
2017
Publisher :
BioMed Central, 2017.

Abstract

Background Slug is a transcription factor that activates the epithelial–mesenchymal transition (EMT) process in cancer progression. The aim of our study was to evaluate the clinical significance of Slug expression in gastric cancer. Methods The expression of Slug in gastric cancer tissues of 456 patients who underwent gastrectomy was evaluated by immunohistochemistry using tissue microarrays. Slug expression level was defined by the composite score determined by multiplying the tumor staining scores for intensity and extent. The associations of Slug expression with clinicopathological characteristics and overall and recurrence-free survival were analyzed. Results Patients were divided into three groups according to Slug composite score (≤4, 6, and 9). Low, mid, and high expression of Slug was observed in 104 (22.7%), 130 (28.3%), and 225 (49.0%) of cases, respectively. Overall survival and recurrence-free survival progressively increased from high to low Slug expression. In terms of lymph node metastasis, the rate of positive lymph node metastasis was 38/104 (36.5%), 79/130 (60.8%), and 178/225 (79.1%) in low, mid, and high Slug expression groups, respectively, displaying a tendency to increase with higher Slug expression. In a multivariate analysis adjusting for patient age, tumor size, tumor depth, and histology, high Slug expression was associated with a high rate of positive lymph node metastasis compared with low Slug expression (odds ratio 3.42; 95% confidence interval, 1.74–6.69). In a subgroup analysis of T1 cancer, patients with negative Slug expression (defined as

Details

Language :
English
ISSN :
14712407
Volume :
17
Database :
OpenAIRE
Journal :
BMC Cancer
Accession number :
edsair.doi.dedup.....3201123d83fed30f5599c6ae4d764722