Co-expression of VEGF-C and survivin predicts poor prognosis in esophageal squamous cell carcinoma

被引:7
作者
Zeng, Yun-Zhu [1 ]
Zhang, Yong-Qu [2 ]
Lin, Xue-Qiong [3 ]
Chen, Jiong-Yu [4 ]
Zhang, Fan [5 ]
Zhu, Jian-Ling [1 ]
Wei, Xiao-Long [1 ]
机构
[1] Shantou Univ, Dept Pathol, Med Coll, Canc Hosp, 7 Raoping Rd, Shantou 515031, Peoples R China
[2] Xiamen Univ, Dept Breast Thyroid Surg, Xiangan Hosp, Xiamen, Peoples R China
[3] Shantou Univ, Med Coll, Canc Hosp, Clin Lab, Shantou, Peoples R China
[4] Shantou Univ, Med Coll, Canc Hosp, Oncol Res Lab, Shantou, Peoples R China
[5] Shantou Univ, Canc Hosp, Guangdong Prov Key Lab Breast Canc Diag & Treatme, Med Coll, Shantou, Peoples R China
关键词
Vascular endothelial growth factor-C (VEGF-C); survivin; esophageal squamous cell carcinoma (ESCC); lymph node metastasis; prognosis; ENDOTHELIAL GROWTH-FACTOR; BREAST-CANCER; EXPRESSION; METASTASIS; LYMPHANGIOGENESIS; OVEREXPRESSION; ASSOCIATION; PROTEIN; ALPHA;
D O I
10.21037/tcr-20-2498
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Lymphatic metastasis is one of the main factors affecting prognosis in esophageal squamous cell carcinoma (ESCC). Vascular endothelial growth factor-C (VEGF-C) is an important factor that promotes lymphangiogenesis. Survivin also plays a significant role in lymphatic invasion. However, the role and mechanism of their co-expression are still unclear in ESCC. The purpose of this study was to investigate whether the co-expression of VEGF-C and survivin could be a potential marker to predict patient prognosis and survival in ESCC. Methods: The levels of VEGF-C, vascular endothelial growth factor receptor 3 (VEGFR-3), survivin, and Ki-67 were determined by immunohistochemistry (IHC) in 97 ESCC patient tumors. The correlations of co-expression of VEGF-C and survivin with pathological features and survival results were also assessed. Results: High VEGF-C expression was observed in 64.9% of the patients and significantly correlated with T stage (P=0.024), node status (P=0.038), and lymph node metastasis (P=0.015). High survivin expression was significantly associated with T stage (P=0.013), N stage (P=0.016), lymph node metastasis (P=0.005), and differentiation (P=0.044) in 67.0% of the patients. Co-expression of VEGF-C and survivin (V+S+) was significantly associated with T stage (P<0.001), N stage (P=0.015), lymph node metastasis (P=0.003), differentiation (P=0.0045), and Ki-67 levels (P=0.024). High expression of VEGF-C or survivin was associated significantly with worse disease-free survival (DFS) and overall survival (OS) (P<0.05). Moreover, the V+S+ group had a worse DFS (P<0.001) and OS (P=0.001) than any other group (i.e., V-S-, V+S-, V-S+) Furthermore, multivariate DFS analyses (95% CI: 1.147-2.220, P=0.006) and multivariate OS analyses (95% CI: 1.080-2.193, P=0.017) revealed that co-expression of VEGF-C and survivin was an independent prognostic factor in ESCC patients. Conclusions: Co-expression of VEGF-C and survivin was predictive of poor prognosis in ESCC. Combined detection of VEGF-C and survivin could represent a feasible and effective marker to predict the prognosis and survival of ESCC patients.
引用
收藏
页码:210 / 222
页数:13
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