胡海亮, 王雷, 陈首慧, 金永堂, 于在诚, 宋超, 李超, 夏觅真, 王怡, 薛绍礼. 非小细胞肺癌患者血浆RAR-β基因甲基化检测及其临床意义[J]. 中国肿瘤临床, 2011, 38(15): 890-893. DOI: 10.3969/j.issn.1000-8179.2011.15.006
引用本文: 胡海亮, 王雷, 陈首慧, 金永堂, 于在诚, 宋超, 李超, 夏觅真, 王怡, 薛绍礼. 非小细胞肺癌患者血浆RAR-β基因甲基化检测及其临床意义[J]. 中国肿瘤临床, 2011, 38(15): 890-893. DOI: 10.3969/j.issn.1000-8179.2011.15.006
Hailiang HU, Lei WANG, Shouhui CHEN, Yongtang JIN, Zaicheng YU, Chao SONG, Chao LI, Mizhen XIA, Yi WANG, Shaoli XUE. Detection and Clinical Significance of RARβ Gene Methylation in the Plasma of Non-Small-Cell Lung Cancer Patients[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2011, 38(15): 890-893. DOI: 10.3969/j.issn.1000-8179.2011.15.006
Citation: Hailiang HU, Lei WANG, Shouhui CHEN, Yongtang JIN, Zaicheng YU, Chao SONG, Chao LI, Mizhen XIA, Yi WANG, Shaoli XUE. Detection and Clinical Significance of RARβ Gene Methylation in the Plasma of Non-Small-Cell Lung Cancer Patients[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2011, 38(15): 890-893. DOI: 10.3969/j.issn.1000-8179.2011.15.006

非小细胞肺癌患者血浆RAR-β基因甲基化检测及其临床意义

Detection and Clinical Significance of RARβ Gene Methylation in the Plasma of Non-Small-Cell Lung Cancer Patients

  • 摘要: 检测非小细胞肺癌(non-small cell lung cancer patients,NSCLC)患者组织和血浆中RAR-β基因甲基化状态,探讨RAR-β基因甲基化在NSCLC筛查和早期诊断中的临床意义。方法:选择120例NSCLC患者,用巢式甲基化特异性聚合酶链反应(nested methylation-specific PCR,nMSP)检测肺癌组织、癌旁组织和外周血血浆RAR-β基因的甲基化,并对120例正常对照组血浆样品进行RAR-β基因甲基化检测,各组检测结果进行比较。结果:肺癌组织RAR-β基因甲基化率59.2%,高于癌旁组织的17.5%(P<0.001);NSCLC患者血浆样品中RAR-β基因甲基化检测率为27.5%,对照组血浆未检测到RAR-β基因甲基化(P<0.001);肺癌患者血浆样品与癌组织RAR-β基因甲基化检出率有显著相关性(P<0.001);血浆中RAR-β基因的甲基化检出率与NSCLC临床分类、临床分期和病理类型均无明显相关性。结论:利用nMSP法对血浆样本RAR-β基因甲基化的检测可为肺癌的早期筛查和诊断提供有价值的信息。

     

    Abstract: Abstract Objective: To detect the methylation status of the retinoic acid receptor-β ( RAR-β ) gene in the plasma and tissues of non-small cell lung cancer (NSCLC) patients and to evaluate its clinical significance in screening and early diagnosis of NSCLC. Methods: A total of 120 NSCLC patients were enrolled, and nested methylation-specific polymerase chain reaction ( nMSP ) was used to determine the methylation of the RAR-β gene in the DNA of the lung cancer cells, paraneoplastic tissues, and plasma from peripheral blood. The determination was also conducted on 120 normal blood samples. The results of the groups were compared. Results: The total frequency of the RAR-β methylation was 59.2% in lung cancer tissues, which was significantly higher than that in the nonmalignant tissues at 17.5% ( P < 0.001 ). The detection rate of hypermethylation for RAR-β gene was 27.5% in the plasma of the 120 NSCLC cases, and no methylated RAR-β gene was found in the plasma of the control group ( P < 0.001 ). There were significant differences in the detection rate of the methylation of RAR-β gene between the lung cancer tissues and the plasma of NSCLC patients ( P < 0.001 ). The detection rate of hypermethylation in the plasma did not significantly correlate with the clinical classification, the pathologic types, and clinical staging of the NSCLC. Conclusion: Detection of RAR-β gene methylation in the plasma of NSCLC patients using nMSP might provide valuable information for early screening and diagnosis of the NSCLC.

     

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