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Diagnostic utility of LunX mRNA in peripheral blood and pleural fluid in patients with primary non-small cell lung cancer

机译:LunX mRNA在原发性非小细胞肺癌患者外周血和胸水中的诊断价值

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Background Progress in lung cancer is hampered by the lack of clinically useful diagnostic markers. The goal of this study was to provide a detailed evaluation of lung cancer tumor markers indicative of molecular abnormalities and to assess their diagnostic utility in non-small cell lung cancer (NSCLC) patients. Methods Quantitative real-time RT-PCR was used to determine LunX, CK19, CEA, VEGF-C and hnRNP A2/B1 mRNA levels in peripheral blood and pleural fluid from NSCLC patients, compared with those from patients with other epithelial cancer (esophagus cancer and breast cancer), benign lung disease (pneumonia and tuberculo pleurisy) and from healthy volunteers. Results In peripheral blood LunX mRNA was detectable in 75.0% (33/44) of patients with NSCLC, but not in patients with other epithelial cancer (0/28), benign lung disease (0/10) or in healthy volunteers (0/15). In contrast, all other genetic markers were detected in patients with either NSCLC, other epithelia cancer or benign lung disease, and in healthy volunteers. The expression level and positive rate of LunX mRNA in peripheral blood correlated with the pathologic stage of NSCLC (P Conclusion Of several commonly used genetic markers, LunX mRNA is the most specific gene marker for lung cancer and has potential diagnostic utility when measured in the peripheral blood and pleural fluid of NSCLC patients.
机译:背景技术缺乏临床上有用的诊断标记物阻碍了肺癌的进展。这项研究的目的是对指示分子异常的肺癌肿瘤标志物进行详细评估,并评估其在非小细胞肺癌(NSCLC)患者中的诊断作用。方法与其他上皮癌(食道癌)患者相比,采用实时定量RT-PCR检测NSCLC患者外周血和胸水中LunX,CK19,CEA,VEGF-C和hnRNP A2 / B1 mRNA的水平和乳腺癌),良性肺部疾病(肺炎和结核性胸膜炎)以及健康志愿者。结果在NSCLC患者中75.0%(33/44)的外周血中可检测到LunX mRNA,但在其他上皮癌(0/28),良性肺部疾病(0/10)或健康志愿者(0 / 15)。相反,在患有NSCLC,其他上皮癌或良性肺部疾病的患者以及健康志愿者中检测到所有其他遗传标记。外周血中LunX mRNA的表达水平和阳性率与NSCLC的病理分期相关(P结论在几种常用的遗传标记中,LunX mRNA是肺癌最特异性的基因标记,在外周血中检测具有潜在的诊断价值非小细胞肺癌患者的血液和胸水。

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