Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Anticancer Res. 2012 Sep;32(9):3917-22.
The primary risk factor for chronic obstructive pulmonary disease (COPD) and non-small cell lung cancer (NSCLC) is cigarette smoking but shared susceptibility factors, such as variations in the matrix metalloproteinase-1 (MMP1) gene, may also underlie both diseases.
Cases with prevalent COPD (n=167), incident NSCLC (n=242), or prevalent COPD plus incident NSCLC (n=128) were compared to disease-free controls (n=338) to assess six MMP1 polymorphisms. The association between these polymorphisms and survival in NSCLC was also evaluated.
Rs11292517 among African-Americans [odds ratio (OR)=5.48, 95% confidence interval (CI)=1.17-25.72] and rs2071230 among Caucasians (OR=2.51, 95% CI=1.09-5.77) appeared to be associated with NSCLC risk in the presence of COPD. Rs470558 appeared to be associated with survival in NSCLC among African-Americans (hazard ratio=3.94; 95%CI=1.14-13.63). No associations remained after adjusting for multiple comparisons.
Polymorphisms in MMP1 were not consistently associated with prevalent COPD or incident NSCLC nor with survival in NSCLC.
慢性阻塞性肺疾病(COPD)和非小细胞肺癌(NSCLC)的主要危险因素是吸烟,但基质金属蛋白酶-1(MMP1)基因等共同的易感因素也可能是这两种疾病的基础。
将患有慢性阻塞性肺病(COPD)(n=167)、新发 NSCLC(n=242)或 COPD 合并 NSCLC(n=128)的病例与无疾病对照(n=338)进行比较,以评估 MMP1 的 6 种基因多态性。还评估了这些多态性与 NSCLC 患者生存的关系。
在 COPD 存在的情况下,非洲裔美国人中的 rs11292517(比值比[OR]=5.48,95%置信区间[CI]=1.17-25.72)和高加索人中的 rs2071230(OR=2.51,95%CI=1.09-5.77)似乎与 NSCLC 风险相关。rs470558 似乎与非洲裔美国人 NSCLC 患者的生存相关(危险比[HR]=3.94;95%CI=1.14-13.63)。在进行多次比较调整后,没有关联仍然存在。
MMP1 基因多态性与 COPD 的发生或 NSCLC 的发生以及 NSCLC 患者的生存没有一致的相关性。