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TFPI-2 甲基化预示非小细胞肺癌不良预后。

TFPI-2 methylation predicts poor prognosis in non-small cell lung cancer.

机构信息

Department of Thoracic-Cardiac Surgery, The Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, 107 Yanjiangxi Rd., Guangzhou 510120, PR China.

出版信息

Lung Cancer. 2012 Apr;76(1):106-11. doi: 10.1016/j.lungcan.2011.09.005. Epub 2011 Oct 7.

DOI:10.1016/j.lungcan.2011.09.005
PMID:21983100
Abstract

BACKGROUND

Methylation of human tissue factor pathway inhibitor-2 (TFPI-2) gene has been detected in several types of cancer, including non-small cell lung cancer (NSCLC). However, an association between the methylation status of TFPI-2 gene and prognosis has not yet been investigated.

METHODS

Methylation of TFPI-2 gene was examined in a consecutive series of 133 non-metastatic NSCLC patients using methylation-specific PCR (MSP). Univariate and multivariate analyses were conducted to investigate the association between clinical variables and overall survival time.

RESULTS

Methylation of TFPI-2 gene was detected in 36 of 133 patients (27.1%). Of these 36 patients, seventeen individuals (47.2%) carried stage III tumors. The 5-year disease free survival rate among patients carrying methylated TFPI-2 tumors was significantly lower as compared to those with unmethylated TFPI-2 tumors (35.5% versus 6.1%, P<0.0001). Moreover, methylation of TFPI-2 gene was found to be an independent prognostic factor for poor overall survival based on multivariate analysis models (P=0.013), as was age >62 years old (P<0.0001) and TNM stage of disease (P<0.0001).

CONCLUSIONS

The results of the present study suggest that methylation of TFPI-2 gene is an independent factor for an unfavorable prognosis in patients with NSCLC.

摘要

背景

人类组织因子途径抑制物-2(TFPI-2)基因的甲基化已在多种类型的癌症中被检测到,包括非小细胞肺癌(NSCLC)。然而,TFPI-2 基因甲基化状态与预后之间的关联尚未得到研究。

方法

采用甲基化特异性 PCR(MSP)检测 133 例非转移性 NSCLC 患者连续系列中 TFPI-2 基因的甲基化情况。采用单因素和多因素分析来研究临床变量与总生存时间之间的关系。

结果

在 133 例患者中,有 36 例(27.1%)检测到 TFPI-2 基因的甲基化。在这 36 例患者中,17 例(47.2%)患者为 III 期肿瘤。携带甲基化 TFPI-2 肿瘤的患者 5 年无病生存率明显低于未携带甲基化 TFPI-2 肿瘤的患者(35.5%比 6.1%,P<0.0001)。此外,基于多因素分析模型,TFPI-2 基因的甲基化被发现是总生存不良的独立预后因素(P=0.013),年龄>62 岁(P<0.0001)和疾病的 TNM 分期(P<0.0001)也是独立预后因素。

结论

本研究结果表明,TFPI-2 基因甲基化是非小细胞肺癌患者预后不良的独立因素。

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