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作 者:杨华平[1] 吴鄂生[1] 陈清兰[1] 胡成平[1]
机构地区:[1]中南大学湘雅医院呼吸内科,湖南长沙410008
出 处:《医学临床研究》2008年第8期1423-1425,共3页Journal of Clinical Research
摘 要:【目的】研究血管内皮生长因子C(VEGF-C)在非小细胞肺癌(NSCLC)中的表达及其与血管新生和淋巴结转移的关系。【方法】采用免疫组化方法检测40例NSCLC癌组织及10例正常肺支气管黏膜组织VEGF-C的表达,同时检测癌组织CD34、p53及p16基因的表达。【结果】40例NSCLC癌组织VEGF-C阳性表达率为77.8%,显著高于正常肺组织(20%,P<0.01)。40例肺癌组织中,VEGF-C高表达组平均微血管密度(MVD)显著高于其低表达组(P<0.01);有淋巴结转移者VEGF-C表达强度显著高于无淋巴结转移者(P<0.01);吸烟者的VEGF-C表达强度显著高于不吸烟者(P<0.05);p53阳性者VEGF-C表达强度显著高于其阴性者(P<0.01);p16阳性组与阴性组间VEGF-C表达强度比较差异无显著性(P>0.05)。【结论】VEGF-C的表达增高与NSCLC的血管新生程度及其淋巴结转移的形成密切相关,因而在NSCLC的生长、侵袭和淋巴结转移中起重要作用。NSCLC的VEGF-C过表达与抑癌基因p53的突变失活有关,而与p16无关。吸烟可能也是诱导VEGF-C表达上调的因素之一。[Objective]To investigate the expression of VEGF-C in non-small cell lung cancer (NSCLC) and its relationship with tumor angiogenesis and lymph node metastasis. [Methods]Forty tumour specimens resected from patients with NSCLC and 10 normal lung and bronchial mucosa tissues were investigated. The expression of VEGF-C was detected by an immunohistochemical method. Meanwhile the expressions of CD34, p53 and p16 in tumor tissues were also detected, [Results] The positive rate of VEGF-C in NSCLC was 77. 8% which was significantly higher than that in normal lung tissues (20%, P 〈0.01). The mean microvessel density (MVD) was significantly higher in patients with high levels of VEGF-C expression than that in those with low levels of VEGF-C expression ( P 〈0.01). VEGF-C expression was significantly higher in patients with lymph node metastasis than in those without lymph node metastasis ( P 〈0. 01), and higher in patients with smoking than in those without smoking( P 〈0. 05), and higher in patients with p53-positive than in those with p53-negative( P 〈0. 01). There was no correlation between VEGF-C expression and p16 expression( P〉0.05). [Conclusion] There is very close correlation between VEGF-C expression and angiogenesis, lymph node metastasis and p53 expression in NSCLC. Smoking maybe causes the overexpression of VEGF-C in NSCLC.
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