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胃癌组织中H-ras和VEGF的表达与血管生成的关系及其临床意义
Correlation of H-ras and VEGF expressions with neoangiogenesis in gastric carcinomaand its clinical significance
【摘要】 目的:探讨胃癌组织H-ras表达与血管内皮生长因子(vascularendothelialgrowthfactor,VEGF)表达和血管生成的关系。方法:应用免疫组织化学ABC法对60例胃癌组织进行H-ras、VEGF表达和微血管密度(micro-vasculardensity,MVD)检测。结果:MVD与胃癌病灶的大小、浸润深度、淋巴结转移和TNM分期密切相关,t值分别为-2·18、-3·46、-4·52和-3·85,P值分别为0·040、0·001、0·001和0·004;VEGF亦与胃癌病灶的大小、浸润深度、淋巴结转移和TNM分期密切相关,χ2值分别为12·80、11·49、10·43和11·52,P值分别为0·002、0·001、0·005和0·003。H-ras的表达与胃癌分化和Lauren分型相关,χ2值分别为11·85和8·87,P值分别为0·001和0·003;并与VEGF的表达相关,χ2=10·79,P=0·001。生存分析显示,MVD和VEGF的表达均影响胃癌的预后,但仅MVD是影响预后的独立因素;H-ras的表达对胃癌的预后影响较小。结论:激活的H-ras可上调VEGF的表达,参与胃癌血管生成的调节,并影响胃癌组织的分化。
【Abstract】 OBJECTIVE:To investigate the relationship between H-ras,vascular endothelial growth factor (VEGF) expressions and neoangiogenesis in gastric carcinoma. METHODS: The expressions of H-ras, VEGF and microvascular density (MVD) in gastric carcinoma were examined by immunohistochemical staining. RESULTS: There was a close correlation between MVD, VEGF expression and several clinicopathological factors, such as tumor size (t=-2.18, P=0.040, χ~2=12.80, P=0.002), penetrating depth ( t= -3.46, P=0.001, χ~2=11.49, P=0.001), lymph node metastasis (t=-4.52, P=0.001, χ~2=10.43, P=0.005) and TNM stage (t=-3.85, P=0.004, χ~2=11.52, P=0.003). H-ras expression in well-differentiated or intestinal type of gastric carcinom was higher than that in poorly-differentiated or diffused type of gastric carcinoma,χ~2=11.85, P=0.001 or χ~2=8.87, P=0.003. Moreover,VEGF expression was associated with the increased H-ras expression,χ~2=10.79, P=0.001. The survival analysis showed that MVD and VEGF expression affected tumor prognosis, but only MVD was an independent prognostics factor. In contrast,H-ras expression had less influence on prognosis in gastric carcinoma. CONCLUSION: The activated H-ras may participate in angiogenesis through VEGF upregulation and influence tumor differentiation in gastric carcinoma.[
- 【文献出处】 中华肿瘤防治杂志 ,Chinese Journal of Cancer Prevention and Treatment , 编辑部邮箱 ,2006年05期
- 【分类号】R735.2
- 【被引频次】15
- 【下载频次】141