Expression and Significances of Contactin-1 in Human Gastric Cancer
Author(s) -
Jiwei Yu,
ShengHua Wu,
Ruiqi Lu,
Jugang Wu,
Xiaochun Ni,
Gou-cai Zhou,
Hai-guang Jiang,
Linhai Zheng,
Xiaoqiang Li,
Guangye Du,
Bo-jian Jiang
Publication year - 2013
Publication title -
gastroenterology research and practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.622
H-Index - 45
eISSN - 1687-630X
pISSN - 1687-6121
DOI - 10.1155/2013/210205
Subject(s) - medicine , immunostaining , cancer , vascular endothelial growth factor , vegf receptors , pathology , immunohistochemistry , algorithm , mathematics
Background . This study aimed at determining the relationship between vascular endothelial growth factor-C (VEGF-C), vascular endothelial growth factor receptor-3 (VEGFR-3), and contactin-1 (CNTN-1) expression in gastric cancer (GC). Methods . The expression level of CNTN-1 mRNA and CNTN-1 protein of 33 cases was determined using RT-PCR and Western Blot. And 105 cases were immunohistochemically examined for VEGF-C, VEGFR-3, and CNTN-1 expressions. Assessment of lymphatic vessel density (LVD) was also performed by D2-40 immunostaining. Then we analyzed the relationships between VEGF-C, VEGFR-3, and CNTN-1, as well as their correlations with clinicopathologic features, LVD, and survival time. Results . The positivity rate of VEGF-C, VEGFR-3, and CNTN-1 in primary tumor was 56.19%, 64.76%, and 58.09%. The expression of CNTN-1 significantly correlated with VEGF-C ( P < 0.001) and VEGFR-3 ( P < 0.001). All of them were closely related to TNM stage, lymphatic invasion, and lymph node involvement ( P < 0.05). LVD was significantly correlated with VEGF-C ( P = 0.001), VEGFR-3 ( P = 0.011), and CNTN-1 expression ( P < 0.001). VEGF-C, VEGFR-3, and CNTN-1 expression significantly associated with poorer prognosis ( P < 0.001, P = 0.034, P = 0.012, resp.). Conclusion . CNTN-1 associated with VEGF-C and VEGFR-3 expression in GC. All of them correlated with lymphatic metastasis, which might play an important role in the lymphatic invasion via lymphangiogenesis pathway in GC.
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