首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >Expression of DPC4/Smad4 in non-small-cell lung carcinoma and its relationship with angiogenesis.
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Expression of DPC4/Smad4 in non-small-cell lung carcinoma and its relationship with angiogenesis.

机译:DPC4 / Smad4在非小细胞肺癌中的表达及其与血管生成的关系。

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The DPC4 influences tumourigenesis and tumor progression by various mechanisms, including angiogenesis. The aim of this study was to determine whether the expression of DPC4 is related to the angiogenesis in lung cancer and whether it could be involved in its clinical behaviour. Immunohistochemistry revealed that DPC4 was expressed at high level in normal broncho-tracheal epithelium, but at low level in tumor tissues, and closely correlated with tumor lymph node metastasis. This result was further confirmed by Western blot analysis. Furthermore, carcinomas with high DPC4 expression demonstrated low VEGF expression and low MVD (microvessel density) labelled with CD34. In addition, DPC4 siRNA in A549 cells also showed that DPC4 could decrease VEGF protein and mRNA expression, and increase TSP1 protein and mRNA expression. Our findings indicated that DPC4 might be an important biomarker for malignant transformation and be involved in preventing the tumor metastasis by inhibiting tumor angiogenesis. Key words: DPC4, Lung cancer, VEGF, TSP-1, Angiogenesis.
机译:DPC4通过多种机制(包括血管生成)影响肿瘤发生和肿瘤进展。这项研究的目的是确定DPC4的表达是否与肺癌中的血管生成有关,以及它是否可能参与其临床行为。免疫组织化学显示,DPC4在正常支气管气管上皮中高表达,在肿瘤组织中低表达,并与肿瘤淋巴结转移密切相关。蛋白质印迹分析进一步证实了该结果。此外,高DPC4表达的癌表现出低VEGF表达和低CD34标记的MVD(微血管密度)。此外,A549细胞中的DPC4 siRNA还显示DPC4可以降低VEGF蛋白和mRNA表达,并增加TSP1蛋白和mRNA表达。我们的发现表明,DPC4可能是恶性转化的重要生物标志物,并通过抑制肿瘤血管生成而参与预防肿瘤转移。关键词:DPC4,肺癌,VEGF,TSP-1,血管生成。

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