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CTLA-4 +49A>G 多态性与晚期非小细胞肺癌的预后相关。

CTLA-4 +49A>G polymorphism is associated with advanced non-small cell lung cancer prognosis.

机构信息

Shandong Provincial Key Laboratory of Radiation Oncology, Shandong Academy of Medical Sciences, Jinan, China.

出版信息

Respiration. 2011;82(5):439-44. doi: 10.1159/000329345. Epub 2011 Aug 11.

Abstract

BACKGROUND

Cytotoxic T lymphocyte antigen 4 (CTLA-4) is a potent immunoregulatory molecule that suppresses antitumor response by downregulating T cell activation. The most studied +49A>G polymorphism of the CTLA-4 gene has been associated with several autoimmune diseases. However, little is known about the association between this functional polymorphism of CTLA-4 and cancer prognosis.

OBJECTIVE

To investigate the association between CTLA-4 +49A>G polymorphism and prognosis of advanced non-small cell lung cancer (NSCLC) patients in a Chinese population.

METHODS

The CTLA-4 +49A>G polymorphism was detected by polymerase chain reaction-restriction fragment length polymorphism in 338 advanced NSCLC patients.

RESULTS

The frequencies of CTLA-4 +49 GG, GA and AA in advanced NSCLC patients were 44.4%, 42.0% and 13.6%, respectively. No significant association was observed between CTLA-4 +49A>G polymorphism and clinicopathologic features of advanced NSCLC including gender, histopathological type, clinical stage and tumor markers. Patients with the AA genotype had a survival time of 9.8 months, significantly shorter than those with the GG genotype (12.5 months) or the GA genotype (12.0 months) (p < 0.001; log-rank test). Multivariate Cox analysis further revealed that the CTLA-4 +49AA genotype is an independent adverse prognostic indicator for NSCLC patients.

CONCLUSION

Our data suggest that the polymorphism of CTLA-4 +49A>G is a prognostic predictor for advanced NSCLC.

摘要

背景

细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)是一种有效的免疫调节分子,通过下调 T 细胞激活来抑制抗肿瘤反应。CTLA-4 基因最受研究的+49A>G 多态性与多种自身免疫性疾病有关。然而,关于 CTLA-4 这一功能多态性与癌症预后之间的关系知之甚少。

目的

在中国人群中,研究 CTLA-4+49A>G 多态性与晚期非小细胞肺癌(NSCLC)患者预后的关系。

方法

采用聚合酶链反应-限制性片段长度多态性检测 338 例晚期 NSCLC 患者 CTLA-4+49A>G 多态性。

结果

晚期 NSCLC 患者 CTLA-4+49 GG、GA 和 AA 的频率分别为 44.4%、42.0%和 13.6%。CTLA-4+49A>G 多态性与晚期 NSCLC 的临床病理特征(包括性别、组织病理学类型、临床分期和肿瘤标志物)无显著相关性。AA 基因型患者的生存时间为 9.8 个月,明显短于 GG 基因型(12.5 个月)或 GA 基因型(12.0 个月)(p<0.001;log-rank 检验)。多因素 Cox 分析进一步表明,CTLA-4+49AA 基因型是 NSCLC 患者的独立预后不良指标。

结论

我们的数据表明,CTLA-4+49A>G 多态性是晚期 NSCLC 的预后预测指标。

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