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非小细胞肺癌中Reprimo以及14-3-3 Σ基因启动子异常甲基化检测[J]. 肿瘤防治研究, 2009, 36(02): 106-109. DOI: 10.3971/j.issn.1000-8578.2009.02.007
引用本文: 非小细胞肺癌中Reprimo以及14-3-3 Σ基因启动子异常甲基化检测[J]. 肿瘤防治研究, 2009, 36(02): 106-109. DOI: 10.3971/j.issn.1000-8578.2009.02.007
Detection of Aberrant Methylation of Reprimo and 14-3-3 Σ Genes in Non-small Cell Lung Cancer[J]. Cancer Research on Prevention and Treatment, 2009, 36(02): 106-109. DOI: 10.3971/j.issn.1000-8578.2009.02.007
Citation: Detection of Aberrant Methylation of Reprimo and 14-3-3 Σ Genes in Non-small Cell Lung Cancer[J]. Cancer Research on Prevention and Treatment, 2009, 36(02): 106-109. DOI: 10.3971/j.issn.1000-8578.2009.02.007

非小细胞肺癌中Reprimo以及14-3-3 Σ基因启动子异常甲基化检测

Detection of Aberrant Methylation of Reprimo and 14-3-3 Σ Genes in Non-small Cell Lung Cancer

  • 摘要: 目的 探讨Reprimo以及14-3-3 Σ基因启动子在非小细胞肺癌(NSCLC)中的异常甲基化状态及其与临床病理资料的联系。方法 采用甲基化特异性聚合酶链反应(Methylation Specific-PCR,MSP)技术检测60例NSCLC以及癌旁正常组织中Reprimo以及14-3-3 Σ基因启动子异常甲基化状态。结果 Reprimo以及14-3-3 Σ基因启动子异常甲基化在NSCLC组织中发生频率分别为36.67%(22/60)和28.33%(17/60),与癌旁正常组织具有显著性差异(P值分别为0.000和0.002)。Reprimo基因启动子异常甲基化频率与吸烟习惯以及年龄相关;14-3-3 Σ启动子异常甲基化与年龄、吸烟习惯、性别、病理类型和临床分期以及淋巴结转移等无相关。结论 NSCLC中存在Reprimo和14-3-3 Σ等基因启动子较高频率的异常甲基化。

     

    Abstract: Objective To investigate the frequency of aberrant methylation of Reprimo and 14-3-3 Σ in non-small cell lung cancer (NSCLC). Methods Aberrant methylation of Reprimo and 14-3-3 Σ were examined by methylation specific-PCR (MSP) in primary NSCLC and normal lung tissues (n = 60). Results Aberrant methylation of Reprimo and 14-3-3 Σ were found to be present in 36.67% and 28.33% of all NSCLC patients respectively.Three cases of Aberrant methylation of Reprimo(5%) and 4 cases of 14-3-3 Σ(6.67%) were detected in normal lung tissues. The frequencies of aberrant methylation of Reprimo and 14-3-3 Σ between primary NSCLC and normal lung tissue group were significantly different. Aberrant methylation of Reprimo was more frequently observed in older patients group (P=0.047) and smoking group (P=0.038). There was no significant correlation between Reprimo methylation frequencies and sex, pathology type, clinical staging and lymphatic metastasis. Similarly no significant association was found between 14-3-3 Σ methylation frequencies and sex, age, pathology type, clinical staging, smoking habit and lymphatic metastasis. Conclusion Methylation of Reprimo and 14-3-3 Σ may play an important role in the pathogenesis of NSCLC.

     

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