CD44v6, MMP-7 and nuclear Cdx2 are significant biomarkers for prediction of lymph node metastasis in primary gastric cancer

被引:93
作者
Okayama, Hirokazu [1 ]
Kumamoto, Kensuke [1 ]
Saitou, Katsuharu [1 ]
Hayase, Suguru [1 ]
Kofunato, Yasuhide [1 ]
Sato, Yu [1 ]
Miyamoto, Kotaro [1 ]
Nakamura, Izumi [1 ]
Ohki, Shinji [1 ]
Sekikawa, Kouji [2 ]
Takenoshita, Seiichi [1 ]
机构
[1] Fukushima Med Univ, Dept Organ Regulatory Surg, Sch Med, Fukushima 9601295, Japan
[2] Kawasaki Saiwai Hosp, Dept Surg, Kanagawa 2120021, Japan
关键词
CD44v6; MMP-7; Cdx2; lymph node metastasis; gastric cancer; NUCLEOSIDE DIPHOSPHATE KINASE; SIGNIFICANT PROGNOSTIC-FACTOR; INTESTINAL METAPLASIA; CYCLIN B1; COLORECTAL-CANCER; POOR-PROGNOSIS; LUNG-CANCER; EXPRESSION; TUMOR; CARCINOMA;
D O I
10.3892/or_00000496
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to examine the expression of CD44v6, CD54, Cdx2, CXCL5, Cyclin B1, MMP-7, nm23, RCAS1 and Survivin in primary gastric cancer and to investigate whether these molecules were useful in predicting the lymph node status. They were selected as candidates for indicators of lymph node metastasis from various kinds of cancer-associated genes reported previously. In 135 cases of radically resected primary gastric adenocarcinoma, we investigated the association between the expression of these molecules and clinocopathologic factors by immunohistochemistry. The results revealed that the expression of CD44v6 and MMP-7 were significantly associated with lymph node status. By contrast, nuclear Cdx2 expression was found to be inversely correlated with lymph node metastasis. Moreover, multivariate analysis demonstrated that CD44v6, MMP-7 and nuclear Cdx2 were independent predictors for lymph node status. In conclusion, our results suggest that positive expression of both CD44v6 and MMP-7, and negative expression of nuclear Cdx2 may serve as powerful predictors of lymph node metastasis in gastric cancer. Combined evaluation of these markers could be further useful to predict lymph node status clinically.
引用
收藏
页码:745 / 755
页数:11
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