Jia Youchao, Zang Aimin, Jiao Shunchang, Chen Sumei, Yan Fu
Department of Medical Oncology, General Hospital of Chinese PLA, Beijing, People's Republic of China; Department of Oncology, Affiliated Hospital of Hebei University, Hebei, People's Republic of China.
Department of Oncology, Affiliated Hospital of Hebei University, Hebei, People's Republic of China.
Onco Targets Ther. 2016 Mar 21;9:1715-9. doi: 10.2147/OTT.S99581. eCollection 2016.
The purpose of the present study was to determine the relationship between interleukin-18 (IL-18) -607 A/C polymorphism and the risk of non-small-cell lung cancer (NSCLC) and its impact on the serum IL-18 level. The genotyping of IL-18 -607 A/C polymorphism was detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The results showed that the AA/AC genotype distribution in NSCLC patients was significantly higher than that of healthy controls (P=0.02). However, no significant differences were found between the two subgroups when stratified by clinical characteristics. Furthermore, serum IL-18 levels were found to be significantly higher in the NSCLC patients than in the controls (P=0.01) as detected by enzyme-linked immunosorbent assay analysis. There was no correlation between serum IL-18 levels and different genotypes. In conclusion, these findings suggest that IL-18 -607 A/C polymorphism increases the risk of NSCLC in the Chinese population, and this polymorphism could not functionally affect the IL-18 levels.
本研究的目的是确定白细胞介素-18(IL-18)-607 A/C多态性与非小细胞肺癌(NSCLC)风险之间的关系及其对血清IL-18水平的影响。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测IL-18 -607 A/C多态性的基因分型。结果显示,NSCLC患者中AA/AC基因型分布显著高于健康对照组(P=0.02)。然而,按临床特征分层时,两个亚组之间未发现显著差异。此外,通过酶联免疫吸附测定分析发现,NSCLC患者血清IL-18水平显著高于对照组(P=0.01)。血清IL-18水平与不同基因型之间无相关性。总之,这些发现表明,IL-18 -607 A/C多态性增加了中国人群患NSCLC的风险,且这种多态性在功能上不会影响IL-18水平。