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首页> 外文期刊>Oncology letters >Expression of astrocyte elevated gene-1 closely correlates with the angiogenesis of gastric cancer
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Expression of astrocyte elevated gene-1 closely correlates with the angiogenesis of gastric cancer

机译:星形胶质细胞升高基因1的表达与胃癌的血管生成密切相关。

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Previous studies have demonstrated that astrocyte elevated gene-1 (AEG-1) is overexpressed in several cancer types and that its upregulation may promote cell proliferation, cell transformation and tumor progression. The present study investigated the expression and prognostic value of AEG-1 in primary gastric cancer (GC) as well as its role in angiogenesis. The results obtained from real-time reverse transcription polymerase chain reaction and western blotting revealed the upregulation of AEG-1 mRNA (P=0.007) and protein expression (P<0.001) in the majority of cancerous tissues compared with matched adjacent non-cancerous gastric tissues. To further investigate the clinicopathological and prognostic roles of AEG-1, immunohistochemical analysis of 216 GC tissue blocks was performed. The results showed that high AEG-1 expression closely correlated with differentiation degree (P<0.001), T stage (P<0.001), N stage (P=0.003) and M stage (P=0.013). Consistent with the abovementioned results, AEG-1 upregulation was also found to significantly correlate with poor survival in GC patients (P<0.001). Furthermore, carcinomas with elevated AEG-1 expression demonstrated high vascular endothelial growth factor (VEGF) expression and microvessel density, which was labeled by cluster of differentiation 34. In addition, an AEG-1 siRNA assay in MGC-803 cells showed that the AEG-1 gene may promote VEGF and hypoxia-inducible factor-1α protein and mRNA expression. The results of the current study indicated that AEG-1 may serve as a valuable prognostic marker for GC and may be involved in regulating tumor angiogenesis.
机译:先前的研究表明,星形胶质细胞升高的基因1(AEG-1)在几种癌症类型中过表达,其上调可能促进细胞增殖,细胞转化和肿瘤进展。本研究调查了AEG-1在原发性胃癌(GC)中的表达和预后价值及其在血管生成中的作用。实时逆转录聚合酶链反应和蛋白质印迹结果表明,与相邻的非癌性胃癌相比,大多数癌组织中AEG-1 mRNA(P = 0.007)和蛋白表达(P <0.001)上调组织。为了进一步研究AEG-1的临床病理和预后作用,对216个GC组织块进行了免疫组织化学分析。结果表明,高AEG-1表达与分化程度(P <0.001),T期(P <0.001),N期(P = 0.003)和M期(P = 0.013)密切相关。与上述结果一致,还发现AEG-1上调与GC患者的不良生存率显着相关(P <0.001)。此外,具有升高的AEG-1表达的癌表现出高的血管内皮生长因子(VEGF)表达和微血管密度,这由分化簇标记34。此外,MGC-803细胞中的AEG-1 siRNA分析表明,AEG -1基因可能促进VEGF和缺氧诱导因子-1α蛋白和mRNA的表达。目前的研究结果表明,AEG-1可能是GC的重要预后标志物,并可能参与调节肿瘤血管生成。

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