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Expression of vascular endothelial growth factor-C and angiogenesis in esophageal squamous cell carcinoma.

机译:食管鳞状细胞癌中血管内皮生长因子-C的表达和血管生成。

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AIM: To investigate the expression of vascular endothelial growth factor-c (VEGF-C) mRNA and microvessel density (MVD) in human esophageal squamous cell carcinoma (ESCC) and its relationship with clinical significance. METHODS: Specimens obtained from 43 patients undergoing surgical resection for ESCC were used in this study. The expression of VEGF-C mRNA was examined by in situ hybridization. Tumor MVD was determined immunohistochemically with anti-CD31 antibody and estimated by image analysis. Ten sections of adjacent normal mucosa were also examined. RESULTS: VEGF-C mRNA expression was detected in cytoplasm of carcinoma cells. Of the 43 ESCC patients studied, 18 cases (41.9%) were positive for VEGF-C mRNA. No VEGF-C mRNA expression was observed in normal esophageal mucosa. VEGF-C mRNA expression correlated significantly with lymph node metastasis, TNM stage and depth of invasion (P < 0.05). Furthermore, histological grade (differentiation) tended to correlate with VEGF-C mRNA expression, but was notstatistically significant (P > 0.05). In tumor lesions, the MVD was significantly greater than that in normal esophageal mucosa. MVD correlated significantly with lymph node metastasis, TNM stage and depth of invasion (P < 0.05), but not with histological grade (differentiation) (P > 0.05). Lesions with VEGF-C mRNA expression had a significantly higher MVD than that of those without VEGF-C mRNA expression (P < 0.05). CONCLUSION: VEGF-C plays a role in lymphatic metastasis via lymphangiogenesis and angiogenesis in ESCC. VEGF-C is one of the important predictors of the biological behavior in ESCC.
机译:目的:探讨血管内皮生长因子-c(VEGF-C)mRNA和微血管密度(MVD)在人食管鳞癌(ESCC)中的表达及其与临床意义的关系。方法:本研究使用了43例行ESCC手术切除的患者的标本。通过原位杂交检查VEGF-C mRNA的表达。用抗CD31抗体免疫组化测定肿瘤MVD,并通过图像分析进行估计。还检查了相邻正常粘膜的十个切片。结果:在癌细胞的细胞质中检测到VEGF-C mRNA的表达。在研究的43名ESCC患者中,有18例(41.9%)的VEGF-C mRNA阳性。在正常食管粘膜中未观察到VEGF-C mRNA表达。 VEGF-C mRNA的表达与淋巴结转移,TNM分期和浸润深度显着相关(P <0.05)。此外,组织学分级(分化)倾向于与VEGF-C mRNA表达相关,但无统计学意义(P> 0.05)。在肿瘤病变中,MVD明显大于正常食管粘膜中的MVD。 MVD与淋巴结转移,TNM分期和浸润深度显着相关(P <0.05),而与组织学分级(分化)无关(P> 0.05)。具有VEGF-C mRNA表达的病变的MVD明显高于无VEGF-C mRNA表达的病变(P <0.05)。结论:VEGF-C在ESCC中通过淋巴管生成和血管生成参与淋巴转移。 VEGF-C是ESCC中生物学行为的重要预测因子之一。

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