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OPN 多态性与晚期 NSCLC 的化疗反应和预后相关。

OPN Polymorphism Is Related to the Chemotherapy Response and Prognosis in Advanced NSCLC.

机构信息

Department of Oncology, Affiliated Hospital of Binzhou Medical University, China.

Department of Chest Surgery, Affiliated Hospital of Binzhou Medical University, China.

出版信息

Int J Genomics. 2014;2014:846142. doi: 10.1155/2014/846142. Epub 2014 Aug 5.

Abstract

Background. Osteopontin (OPN) is associated with prognosis of patients with non-small-cell lung cancer (NSCLC). However, little is known about the association between OPN gene polymorphism and the chemotherapy response in NSCLC patients. Methods. A total of 497 patients with inoperable advanced stage of NSCLC (stages III B and IV NSCLC) were enrolled. All patients had received platinum-based chemotherapy. OPN gene polymorphisms at 156 GG/G, 443 C/T, and -66T/G were determined. Results. The genotypes and allele frequency of -443C>T were significantly different between the responders and nonresponders. Responders had a markedly higher frequency of -443TT genotype than responders (40.71% versus 19.09%, P < 0.001). With CC as reference, the TT genotype carriers had a higher chance to be well responders (adjusted OR = 4.43, 95% CI: 2.60-7.53, adjusted P < 0.001). The median overall survival time for patients with -443CC, -443CT, and -443TT genotype carriers was significantly different. Multivariate Cox proportional hazards regression models showed that OPN -443C>T gene polymorphisms were closely correlated to poor NSCLC prognosis. Conclusion. OPN -443C>T gene polymorphism may be used as a molecular marker to predict the treatment response to chemotherapy in advanced NSCLC patients.

摘要

背景

骨桥蛋白(OPN)与非小细胞肺癌(NSCLC)患者的预后相关。然而,OPN 基因多态性与 NSCLC 患者化疗反应之间的关系知之甚少。

方法

共纳入 497 例无法手术的晚期 NSCLC(III B 和 IV 期 NSCLC)患者。所有患者均接受了铂类为基础的化疗。检测 OPN 基因 156 GG/G、443 C/T 和-66T/G 多态性。

结果

-443C>T 的基因型和等位基因频率在应答者和无应答者之间存在显著差异。应答者中-443TT 基因型的频率明显高于无应答者(40.71%比 19.09%,P<0.001)。以 CC 为参照,TT 基因型携带者成为完全应答者的可能性更高(调整 OR=4.43,95%CI:2.60-7.53,调整 P<0.001)。-443CC、-443CT 和-443TT 基因型携带者的总生存时间中位数存在显著差异。多因素 Cox 比例风险回归模型显示,OPN-443C>T 基因多态性与 NSCLC 不良预后密切相关。

结论

OPN-443C>T 基因多态性可作为预测晚期 NSCLC 患者化疗反应的分子标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9bb/4139078/4c9e2b0d1b3e/IJG2014-846142.001.jpg

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