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Clinical significance of co-expression of VEGF-C and VEGFR-3 in non-small cell lung cancer

机译:VEGF-C和VEGFR-3在非小细胞肺癌中共表达的临床意义

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Objective To investigate the relationship between vascular endothelial growth factor C (VEGF-C) expression, VEGFR-3 expression, lymphangiogenesis and angiogenesis in human non-small cell lung cancer (NSCLC). Methods Seventy-six NSCLC samples were stained for VEGF-C, VEGFR-3 and CD34 with immunohistochemical methods. Assessment of lymphatic vessel density ( LVD) and microvessel density ( MVD) was performed. The expressions of VEGF-C in 24 fresh NSCLC samples were determined with Western blot assay. Results Of the 76 NSCLC cases, 55 were VEGF-C positive and 40 were VEGFR-3 positive in cancer cells. A significant positive correlation was found between VEGF-C expression and VEGFR-3 expression in cancer cells ( P < 0.05) . VEGF-C expression was negatively associated with differentiation of tumor cells (P<0.05). VEGF-C expression and VEGFR-3 expression were positively associated with lymph node metastasis and lymphatic invasion (P<0.05). LVD was positively related to VEGF-C expression, lymph node metastasis, lymphatic invasion and clinical stage ( P < 0. 05). There was a significant correlation between LVD and MVD ( R = 0.732, P < 0.05). Patients with positive VEGF-C expression had worse outcomes than those with negative VEGF-C expression (P< 0.01). Conclusions In NSCLC, VEGF-C and VEGFR-3 are related to the lymphangiogenesis, angiogenesis, and occurrence and development of lung cancers. VEGF-C expression could be a useful predictor of poor prognosis in NSCLC.
机译:目的探讨人非小细胞肺癌(NSCLC)血管内皮生长因子C(VEGF-C)表达,VEGFR-3表达,淋巴管生成与血管生成之间的关系。方法采用免疫组织化学方法对76例NSCLC患者的VEGF-C,VEGFR-3和CD34进行染色。评估淋巴管密度(LVD)和微血管密度(MVD)。用蛋白质印迹法测定24例新鲜NSCLC样品中VEGF-C的表达。结果76例NSCLC癌细胞中,VEGF-C阳性55例,VEGFR-3阳性40例。癌细胞中VEGF-C表达与VEGFR-3表达呈显着正相关(P <0.05)。 VEGF-C的表达与肿瘤细胞的分化呈负相关(P <0.05)。 VEGF-C和VEGFR-3表达与淋巴结转移和淋巴管浸润呈正相关(P <0.05)。 LVD与VEGF-C表达,淋巴结转移,淋巴管浸润和临床分期呈正相关(P <0。05)。 LVD和MVD之间存在显着相关性(R = 0.732,P <0.05)。 VEGF-C表达阳性的患者比VEGF-C表达阴性的患者的预后较差(P <0.01)。结论在NSCLC中,VEGF-C和VEGFR-3与肺癌的淋巴管生成,血管生成以及发生发展有关。 VEGF-C表达可能是NSCLC预后不良的有用预测指标。

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