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作 者:王丰[1] 华东[1] 吴玉玉[1] 程之红[1] 胡瑜[1] 谢其根[1] 王琼瑶[1] 杜祥[2] 黄朝晖[1]
机构地区:[1]苏州大学附属第四医院肿瘤研究所,江苏无锡214062 [2]复旦大学附属肿瘤医院病理科,复旦大学上海医学院肿瘤学系,上海200032
出 处:《中国癌症杂志》2011年第1期12-16,共5页China Oncology
基 金:江苏省自然科学基金资助项目(No:BK2008114)
摘 要:背景与目的:DNA甲基化是一种新的肿瘤诊断及预后判断的标志物。本研究运用自行建立的甲基化敏感性限制性内切酶-定量PCR(methylation-sensitive restriction enzymes-based quantitative PCR,MSRE-qPCR)方法检测血浆GSTP1和SFRP1基因的DNA甲基化状态,探讨其在肝细胞癌(hepatocellular carcinoma,HCC)早期诊断中的价值。方法:收集150例血浆标本,包括72例HCC,37例肝良性病变和41名健康对照者。用MSRE-qPCR法检测血浆GSTP1和SFRP1基因DNA甲基化水平。结果:HCC患者血浆GSTP1和SFRP1甲基化阳性率分别为54.2%和27.8%,显著高于健康对照组(9.8%和2.4%,P<0.001)和肝良性病变组(10.8%和5.4%,P<0.001);同时检测血浆GSTP1和SFRP1可检出63.9%的HCC;而联合血清AFP分析可进一步将HCC诊断率提高至73.6%。结论:联合检测血浆GSTP1和SFRP1基因DNA甲基化对于HCC早期非侵入性诊断具有重要价值。Background and purpose: DNA methylation is a potential biomarker for tumor diagnosis and prognosis. This study aimed to detect the methylation statuses of GSTP1 and SFRP1 in plasma samples using a methylation-sensitive restriction enzymes-based quantitative PCR (MSRE-qPCR) method as well as to assess its clinical value for early noninvasive diagnosis of hepatocellular carcinoma (HCC). Methods: One hundred and fifty plasma samples from 72 patients with HCC, 37 patients with a benign form of the diseases and 41 normal controls were collected. The methylation statuses of GSTP1 and SFRP1 in these plasma samples were determined using the MSRE-qPCR method. Results: The methylation rates of GSTP1 and SFRP1 in HCC plasma were 54.2% and 27.8%, respectively, which were significantly higher than those in plasma from patients with benign live diseases (9.8% and 2.4%, P〈0.001) and normal controls patients (10.8% and 5.4%, P〈0.001).The combination analysis of GSTP1 and SFRP1 methylation detected 63.9% of all HCC cases. The combined analysis of using both plasma methylation and serum AFP revealed an elevated detection rate of 73.6%. Conclusion: Plasma DNA methylation analysis of GSTP1 and SFRP1 is a valuable tool for an early noninvasive diagnosis of HCC.
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