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中国人群中PD-L1基因多态性与非小细胞肺癌易感性及临床结局的关联

The association of PD-L1 gene polymorphisms with non-small-cell lung cancer susceptibility and clinical outcomes in a Chinese population.

作者信息

Zhao Xiaolong, Peng Yu, Li Xuemei, Zhang Shiheng, Peng Yang, Shan Jinlu, Li Mengxia, Dai Nan, Feng Yan, Xu Chengxiong, Wang Dong

机构信息

Cancer Center, Daping Hospital, Army Medical University (Third Military Medical University) Chongqing, China.

出版信息

Int J Clin Exp Pathol. 2020 Aug 1;13(8):2130-2136. eCollection 2020.

Abstract

OBJECTIVE

To investigate the influence of PD-L1 polymorphisms on the susceptibility of non-small-cell lung cancer (NSCLC) and the prognosis of NSCLC patients who undergo platinum-based chemotherapy.

MATERIALS AND METHODS

9 single nucleotide polymorphisms (SNPs) in the PD-L1 gene, including rs822336 (G>C), rs822337 (T>A), rs10815225 (G>C), rs7866740 (C>G), rs866066 (C>T), rs822338 (C>T), rs2890657 (C>G), rs2890658 (C>A), and rs229136 (C>G) were selected for this study. Genotyping was performed in 281 advanced NSCLC patients and 251 healthy volunteers using the matrix assisted laser desorption ionization time-of-flight (MALDI-TOF) method.

RESULTS

The G allele of PD-L1 rs7866740 was significantly related to the risk of NSCLC. Compared with the C allele, the G allele an increase the risk of NSCLC (OR=3.532, 95% CI: 1.232-10.129, =0.001). In terms of the clinical outcomes, PD-L1 rs2890658 C>A was significantly associated with both a worse progression-free survival (adjusted HR=1.367, 95% CI=1.0-1.8, =0.038) and a worse overall survival (adjusted HR=1.402, 95% CI=1.0-1.9, =0.026) of NSCLC patients. PD-L1 rs822336 G>C was significantly related to a worse overall survival (adjusted HR=1.393, 95% CI=1.1-1.8, =0.021).

CONCLUSIONS

PD-L1 rs7866740 C>G may play a role in the pathogenesis of NSCLC. PD-L1 rs2890658 C>A and rs822336 G>C are related to the prognoses of patients receiving platinum-based chemotherapy.

摘要

目的

探讨程序性死亡受体配体1(PD-L1)基因多态性对非小细胞肺癌(NSCLC)易感性及接受铂类化疗的NSCLC患者预后的影响。

材料与方法

本研究选取了PD-L1基因中的9个单核苷酸多态性(SNP),包括rs822336(G>C)、rs822337(T>A)、rs10815225(G>C)、rs7866740(C>G)、rs866066(C>T)、rs822338(C>T)、rs2890657(C>G)、rs2890658(C>A)和rs229136(C>G)。采用基质辅助激光解吸电离飞行时间(MALDI-TOF)法对281例晚期NSCLC患者和251例健康志愿者进行基因分型。

结果

PD-L1基因rs7866740的G等位基因与NSCLC风险显著相关。与C等位基因相比,G等位基因增加了NSCLC风险(比值比[OR]=3.532,95%置信区间[CI]:1.232-10.129,P=0.001)。在临床结局方面,PD-L1基因rs2890658 C>A与NSCLC患者较差的无进展生存期(校正风险比[HR]=1.367,95%CI=1.0-1.8,P=0.038)和较差的总生存期(校正HR=1.402,95%CI=1.0-1.9,P=0.026)均显著相关。PD-L1基因rs822336 G>C与较差的总生存期显著相关(校正HR=1.393,95%CI=1.1-1.8,P=0.021)。

结论

PD-L1基因rs7866740 C>G可能在NSCLC发病机制中起作用。PD-L1基因rs2890658 C>A和rs822336 G>C与接受铂类化疗患者的预后相关。

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