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用于肺癌诊断的支气管肺泡灌洗液中SHOX2和RASSF1A基因座的DNA甲基化分析

DNA Methylation Analysis of the SHOX2 and RASSF1A Panel in Bronchoalveolar Lavage Fluid for Lung Cancer Diagnosis.

作者信息

Zhang Chenzi, Yu Wenjun, Wang Lin, Zhao Mingna, Guo Qiaomei, Lv Shaogang, Hu Xiaomeng, Lou Jiatao

机构信息

Department of Laboratory Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai 200030, China.

出版信息

J Cancer. 2017 Sep 30;8(17):3585-3591. doi: 10.7150/jca.21368. eCollection 2017.

Abstract

Currently the majority of lung cancer patients are diagnosed as advanced diseases for no sensitive and specific biomarkers exist, noninvasive biomarkers with high sensitivity and specificity are urgently needed in lung cancer diagnosis. Bronchoscopy is a standard procedure of the diagnostic work-up of patients with suspected lung cancer despite of the limited diagnostic accuracy. Besides, epigenetic changes through DNA methylation play an important role in tumorigenesis. Thus, we examined the aberrant methylation of the SHOX2 and RASSF1A in bronchoalveolar lavage fluid (BALF) in comparing with conventional cytology examination and serum CEA in order to evaluate the new diagnostic method. BALF and serum samples were collected from 322 patients at the time of diagnosis, 284 of them were pathologically confirmed lung cancer, 35 were benign lung diseases and 3 were malignancies in other systems. For all of the 322 patients, the methylation status of the SHOX2 and RASSF1A gene were detected by a new RT-PCR platform and then confirmed by sanger sequencing. Serum CEA were detected using electrochemiluminescence immunoassay. Profiling data showed the consistency of RT-PCR and sanger sequencing in detecting the methylation of the SHOX2 and RASSF1A. Besides, the combination of SHOX2 and RASSF1A methylation in BALF yielded a diagnostic sensitivity of 81.0% and specificity of 97.4%. When compared with established cytology examination (sensitivity: 68.3%, specificity: 97.4%) and serum biomarker carcinoembryonic antigen (CEA) (sensitivity: 30.6%, specificity: 100.0%), the SHOX2 and RASSF1A methylation panel showed the highest diagnostic efficiency. Notably, the combination of cytology and the SHOX2 and RASSF1A methylation panel could significantly improve the diagnostic efficacy. The methylation analysis of the SHOX2 and RASSF1A panel in BALF with RT-PCR achieved a satisfactory sensitivity and specificity in lung cancer diagnosis, especially in an early stage. It could be used as a promising noninvasive biomarker for auxiliary diagnosis of lung cancer.

摘要

目前,由于缺乏敏感且特异的生物标志物,大多数肺癌患者被诊断为晚期疾病,肺癌诊断迫切需要高灵敏度和特异性的非侵入性生物标志物。支气管镜检查是疑似肺癌患者诊断性检查的标准程序,尽管其诊断准确性有限。此外,DNA甲基化引起的表观遗传变化在肿瘤发生中起重要作用。因此,我们检测了支气管肺泡灌洗液(BALF)中SHOX2和RASSF1A的异常甲基化,并与传统细胞学检查和血清癌胚抗原(CEA)进行比较,以评估这种新的诊断方法。在诊断时从322例患者中采集BALF和血清样本,其中284例经病理证实为肺癌,35例为良性肺病,3例为其他系统恶性肿瘤。对所有322例患者,通过新的RT-PCR平台检测SHOX2和RASSF1A基因的甲基化状态,然后通过桑格测序进行确认。采用电化学发光免疫分析法检测血清CEA。分析数据显示RT-PCR和桑格测序在检测SHOX2和RASSF1A甲基化方面具有一致性。此外,BALF中SHOX2和RASSF1A甲基化联合检测的诊断敏感性为81.0%,特异性为97.4%。与既定的细胞学检查(敏感性:68.3%,特异性:97.4%)和血清生物标志物癌胚抗原(CEA)(敏感性:30.6%,特异性:100.0%)相比,SHOX2和RASSF1A甲基化检测组显示出最高的诊断效率。值得注意的是,细胞学检查与SHOX2和RASSF1A甲基化检测组联合使用可显著提高诊断效能。采用RT-PCR对BALF中的SHOX2和RASSF1A检测组进行甲基化分析,在肺癌诊断中,尤其是早期诊断中,获得了令人满意的敏感性和特异性。它可作为一种有前景的非侵入性生物标志物用于肺癌的辅助诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd95/5687174/f9d4dcf0208a/jcav08p3585g001.jpg

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