Korean J Clin Oncol.  2018 Dec;14(2):89-94. 10.14216/kjco.18016.

Clinicopathologic correlation with MUC expression in advanced gastric cancer

Affiliations
  • 1Department of Surgery, Seoul Paik Hospital, Inje University College of Medicine, Seoul, Korea. yongaaa5972@naver.com

Abstract

PURPOSE
To investigate the relationship between MUC expression and clinicopathologic factors in advanced gastric cancer.
METHODS
A total of 237 tumor specimens were assessed for MUC expression by immunohistochemistry. The clinicopathologic factors were investigated with MUC1, MUC2, MUC5AC, and MUC6.
RESULTS
MUC1, MUC2, MUC5AC, and MUC6 expression was identified in 148 of 237 (62.4%), 141 of 237 (59.5%), 186 of 237 (78.5%), and 146 of 237 (61.6%) specimens, respectively. MUC1 expression was correlated with age, human epidermal growth factor receptor 2 (HER2) status, lymphatic invasion, Lauren classification and histology. Further multivariate logistic regression analysis revealed a significant correlation between MUC1expression and lymphatic invasion, diffuse type of Lauren classification. MUC5AC expression was correlated with HER2 status, Lauren classification and histology. Further multivariate logistic regression analysis revealed a significant correlation between MUC5AC expression and HER2 status, diffuse and mixed type of Lauren classification. MUC2 and MUC6 expression were not correlated with clinicopathologic factors. The patients of MUC1 expression had poorer survival than those without MUC1 expression, but MUC2, MUC5AC or MUC6 were not related to survival. In an additional multivariate analysis that used the Cox proportional hazards model, MUC1 expression was not significantly correlated with patient survival independent of age, N-stage, and venous invasion.
CONCLUSION
When each of these four MUCs expression is evaluated, in light of clinicopathologic factors, MUC1 expression may be considered as a prognostic factor in patients with advanced gastric cancer. Therefore, careful follow-up may be necessary because the prognosis is poor when MUC1 expression is present.

Keyword

MUC; Stomach neoplasms; Prognosis; Retrospective analysis

MeSH Terms

Classification
Follow-Up Studies
Humans
Immunohistochemistry
Logistic Models
Multivariate Analysis
Prognosis
Proportional Hazards Models
Receptor, Epidermal Growth Factor
Stomach Neoplasms*
Receptor, Epidermal Growth Factor
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