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[RUNX3启动子高甲基化与早期手术切除的非小细胞肺癌的预后]

[RUNX3 promoter hypermethylation and prognosis of early surgically resected non-small cell lung cancers].

作者信息

Tang Yan, Wu Fang, Hu Chunhong

机构信息

Department of Oncology, Second Xiangya Hospital, Central South University, Changsha 41001, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Jul;36(7):650-4. doi: 10.3969/j.issn.1672-7347.2011.07.012.

DOI:10.3969/j.issn.1672-7347.2011.07.012
PMID:21873791
Abstract

OBJECTIVE

To determine the relation between the promoter methylation status of RUNX3 gene and clinicopathological parameters, prognosis of non-small cell lung cancer (NSCLC).

METHODS

We collected 80 formalin-fixed paraffin-embedded lung cancer tissue samples from NSCLC patients who received postoperative adjuvant chemotherapy with cisplatin. Genomic DNA was extracted through phenol/chloroform extraction. The methylation status of RUNX3 was determined by nested methylation-specific PCR (nMSP). We investigated the pathological and prognostic characteristics of NSCLC stratified by methylation status.

RESULTS

The RUNX3 promoter methylation was observed in 20 of the 80 NSCLC samples (25.0%). Methylation of RUNX3 was more frequent in adenocarcinomas (36%) than in squamous cell carcinomas (11%) (P=0.020). In multivariate Logistic regression, positive RUNX3 methylation status (P=0.011) was found to be independent disease-free survival factor as was N stage (P<0.001). Kaplan-Meier curves showed patients with RUNX3 methylation had a significantly poorer overall survival than those without methylation (P=0.003; log-rank test). In multivariate Cox proportional hazards regression analysis, RUNX3 methylation (RR:2.345, 95% CI:1.30-4.865, P=0.022) was a significant independent prognostic factor for the overall survival.

CONCLUSION

RUNX3 methylation is a significant independent prognostic factor for disease-free survival and overall survival.

摘要

目的

确定RUNX3基因启动子甲基化状态与非小细胞肺癌(NSCLC)临床病理参数及预后之间的关系。

方法

我们收集了80例接受顺铂术后辅助化疗的NSCLC患者的福尔马林固定石蜡包埋肺癌组织样本。通过酚/氯仿提取法提取基因组DNA。采用巢式甲基化特异性PCR(nMSP)检测RUNX3的甲基化状态。我们根据甲基化状态对NSCLC的病理和预后特征进行了研究。

结果

80例NSCLC样本中有20例(25.0%)观察到RUNX3启动子甲基化。RUNX3甲基化在腺癌(36%)中比在鳞状细胞癌(11%)中更常见(P=0.020)。在多因素Logistic回归分析中,发现RUNX3甲基化阳性状态(P=0.011)与N分期(P<0.001)一样是独立的无病生存因素。Kaplan-Meier曲线显示,RUNX3甲基化患者的总生存期明显低于未甲基化患者(P=0.003;对数秩检验)。在多因素Cox比例风险回归分析中,RUNX3甲基化(RR:2.345,95%CI:1.30 - 4.865,P=0.022)是总生存期的显著独立预后因素。

结论

RUNX3甲基化是无病生存期和总生存期的显著独立预后因素。

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