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RAS 关联结构域家族蛋白 1A 的甲基化作为肺癌的生物标志物。

Methylation of RAS association domain family protein 1A as a biomarker of lung cancer.

作者信息

Grote Hans Juergen, Schmiemann Viola, Geddert Helene, Bocking Alfred, Kappes Rainer, Gabbert Helmut Erich, Sarbia Mario

机构信息

Institute of Cytopathology, Heinrich Heine University, Duesseldorf, Germany.

出版信息

Cancer. 2006 Apr 25;108(2):129-34. doi: 10.1002/cncr.21717.

Abstract

BACKGROUND

Promoter hypermethylation is an important mechanism for silencing tumor-suppressor genes in cancer and a promising tool for development of molecular biomarkers. This study aimed to determine the prevalence of RAS association domain family protein 1A (RASSF1A) promoter hypermethylation in bronchial aspirates of patients with suspected lung cancer and to test whether this type of methylation assay could be used as a diagnostic adjunct to conventional cytology.

METHODS

Two hundred three bronchial aspirates from patients with suspected lung cancer were analyzed for RASSF1A hypermethylation by using a sensitive quantitative methylation-specific polymerase chain reaction (QMSP).

RESULTS

RASSF1A hypermethylation was found in 88% (35 of 40), 28% (31 of 111), and 100% (6 of 6) of bronchial aspirates collected from patients diagnosed with small cell lung cancer, nonsmall cell lung cancer, and combined small cell lung cancer, respectively. No hypermethylation was detected in patients diagnosed with nonneoplastic lung disease (0 of 46). Depending on histologic subtype, up to 82% of cases presenting with a negative histology showed a positive methylation assay.

CONCLUSIONS

The QMSP analysis of RASSF1A hypermethylation enabled a highly specific distinction between patients diagnosed with lung cancer and those with nonneoplastic lung disease. These results suggested that a QMSP assay is a promising molecular tool for diagnosis of primary lung cancer.

摘要

背景

启动子高甲基化是癌症中肿瘤抑制基因沉默的重要机制,也是分子生物标志物开发的一个有前景的工具。本研究旨在确定疑似肺癌患者支气管吸出物中RAS关联结构域家族蛋白1A(RASSF1A)启动子高甲基化的发生率,并测试这种甲基化检测方法是否可作为传统细胞学诊断的辅助手段。

方法

采用灵敏的定量甲基化特异性聚合酶链反应(QMSP)对203例疑似肺癌患者的支气管吸出物进行RASSF1A高甲基化分析。

结果

在分别诊断为小细胞肺癌、非小细胞肺癌和合并小细胞肺癌的患者所采集的支气管吸出物中,RASSF1A高甲基化的检出率分别为88%(40例中的35例)、28%(111例中的31例)和100%(6例中的6例)。在诊断为非肿瘤性肺病的患者中未检测到高甲基化(46例中的0例)。根据组织学亚型,高达82%组织学检查为阴性的病例甲基化检测呈阳性。

结论

RASSF1A高甲基化的QMSP分析能够在诊断为肺癌的患者和非肿瘤性肺病患者之间实现高度特异性的区分。这些结果表明,QMSP检测是诊断原发性肺癌的一种有前景的分子工具。

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