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作 者:张玉霞[1] 陈洪雷[1] 叶波[1] 杨飞[1] 喻伦银[1]
机构地区:[1]武汉大学基础医学院病理学教研室,430071
出 处:《中华病理学杂志》2008年第5期300-304,共5页Chinese Journal of Pathology
基 金:国家自然科学基金资助项目(30500226)
摘 要:目的 检测窖蛋白1(Cav-1)在非小细胞肺癌(NSCLC)中的蛋白表达以及启动子的甲基化状况,探讨Cav-1基因在NSCLC中的作用及其临床意义。方法 应用免疫组织化学(SP法)和量子点Qd600染色检测123例NSCLC组织、17例良性病变肺组织中Cav-1蛋白表达和亚细胞定位。亚硫酸氢钠处理DNA,甲基化特异性PCR(MSP)检测Cav-1基因启动子区域的甲基化水平。结果 Cav-1蛋白在肺支气管黏膜上皮细胞、肺泡上皮细胞、毛细血管内皮细胞、成纤维细胞、平滑肌细胞的胞质和胞膜高表达。癌旁组织(对照)组和肺癌组中Cav-1蛋白的阳性率分别为17/17、43.1%(53/123),两组间差异有统计学意义(P=0.001);Cav-1蛋白在NSCLC不同的组织学类型(P=0.552)和分化程度(P=0.160)中差异均无统计学意义。Cav-1蛋白阳性率与NSCLC的TNM分期(P=0.001)以及淋巴结转移(P=0.001)均相关。在40例Cav-1蛋白表达为阴性的肺癌组织和12例癌旁肺组织,MSP法均未检测到Cav-1基因启动子区域的甲基化。结论 Cav-1蛋白失表达的机制可能与启动子区是否甲基化无关。Cav-1蛋白高表达预示NSCLC恶化进展和高侵袭性。Objective To study the methylation of CpG islands in the promoter region, expression of caveolin 1 (Cav-1) gene and their clinical significance in non-small cell lung cancers (NSCLC). Methods Immunohistochemistry and quanta Qd600 staining were used to detect the expression of Cav-1 in tissues from benign lung lesions ( n = 17 ) and NSCLC ( n = 123). DNA was treated with sodium bisulfite and the Cav-1 promoter region was screened using methylation-specific polymerase chain reaction for the possible methylation sites. Results Cav-1 protein was highly expressed in cytoplasm and cell membrane of normal bronchial epithelium, alveolar epithelium, endothelial cells, fibroblasts and smooth muscle cells. The expression rates of Cav-1 protein were 100% (17/17) in the control group and 43.1% (53/123) in the NSCLC group (P =0. 001). Amongst the NSCLC group, there was no statistically significant difference in Cav-1 protein expression in different histologic types (P =0. 552) and tumor grades (P =0. 160). On the other hand, Cav-1 protein immunoreactivity was remarkably higher in advanced tumor stage: 72. 7% in stage ⅢA +ⅢB, compared with 9.4% in stage I A + I B and 38. 3% in stage ⅡA + ⅡB (P =0. 001 ). The expression rate of Cav-1 protein in the NSCLC cases with lymph node metastasis was 53. 6%, compared with 20.5% in those without nodal involvement (P =0. 001 ). DNA from 40 NSCLC cases with negative Cav-1 protein expression and 12 cases of peritumoral lung tissues were extracted. Methylation in the promoter region of Cav-1 gene was not detected in lung cancer or peritumoral tissues. Conclusions High expression of Cav- 1 protein is respected of the aggressive clinical behavior and advanced tumor stage. Loss of Cav-1 protein expression seems not correlated to the methylation status in the promoter region of Cav-1 gene.
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