Department of Gastroenterology; University of Medicine and Pharmacy, Petru Rares Str. No. 2, Craiova, Romania.
J Gastrointestin Liver Dis. 2010 Jun;19(2):135-9.
The role of angiogenesis in progression and metastasis of gastric cancer has been studied over the last years. The aim of our study was to assess the microvessel density and vascular endothelial growth factor (VEGF) expression in correlation with prognosis, survival and the risk for upper gastrointestinal (GI) bleeding as well.
We prospectively assessed angiogenesis in 40 patients with gastric carcinoma. Microvessel density was calculated using CD31 and CD34 markers, and VEGF expression was assessed in biopsy samples. The tumor stage was established using imaging methods: CT scan for M and N stage and endoscopic ultrasound for T and N stages. The correlation between pathological markers and tumor stage, survival rate and risk of upper gastrointestinal bleeding was assessed.
The study included 40 patients with gastric cancer; among them 8 patients presented with upper GI bleeding. The average microvessel density was 10.21 for CD31 and 11.85 for CD34 in all patients VEGF was positive only in 45% of patients. The microvessel density was higher in patients with advanced TNM stage, and a correlation with the risk of UGIB and survival rate was also found. VEGF expression correlated with TNM stage and with the risk of upper GI bleeding.
Microvessel density (estimated by CD34) was involved in locally advanced disease, while VEGF was correlated with loco-regional extension and distant metastasis in gastric cancer patients. There was a clear correlation between angiogenic parameters, survival rate and the risk of upper GI bleeding.
近年来,人们对血管生成在胃癌进展和转移中的作用进行了研究。本研究的目的是评估微血管密度和血管内皮生长因子(VEGF)的表达与预后、生存以及上消化道(GI)出血风险的相关性。
我们前瞻性评估了 40 例胃癌患者的血管生成情况。使用 CD31 和 CD34 标志物计算微血管密度,并用活检样本评估 VEGF 表达。肿瘤分期采用影像学方法确定:CT 扫描用于 M 和 N 分期,内镜超声用于 T 和 N 分期。评估了病理标志物与肿瘤分期、生存率和上消化道出血风险之间的相关性。
该研究纳入了 40 例胃癌患者;其中 8 例出现上消化道出血。所有患者的平均微血管密度为 CD31 为 10.21,CD34 为 11.85。VEGF 在 45%的患者中呈阳性。微血管密度在 TNM 晚期患者中较高,且与 UGIB 风险和生存率相关。VEGF 表达与 TNM 分期和上消化道出血风险相关。
微血管密度(通过 CD34 评估)与局部晚期疾病相关,而 VEGF 与胃癌患者的局部区域扩展和远处转移相关。血管生成参数与生存率和上消化道出血风险之间存在明显相关性。