Genetic evidence for the causal association between programmed death-ligand 1 and lung cancer

被引:0
作者
Zhao Yang
Rong Yu
Wei Deng
Weihu Wang
机构
[1] The University of Hong Kong,School of Public Health, Li Ka Shing Faculty of Medicine
[2] Peking University Cancer Hospital and Institute,Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology
来源
Journal of Cancer Research and Clinical Oncology | 2021年 / 147卷
关键词
protein quantitative trait loci; PD-L1; Lung cancer; Mendelian randomization; Negative control;
D O I
暂无
中图分类号
学科分类号
摘要
PD-1/PD-L1 might have a causal role in operating lung cancer risk. However, such an association has not been investigated in the general population. We assessed whether PD-L1 has an independent effect on lung cancer risk using two-sample Mendelian randomization (MR) based on a proteomic genome-wide association study (3301 health participants) of European ancestry and the International Lung cancer Consortium (11,348 cases and 15,861 controls). Negative control analyses using chronic obstructive pulmonary disease (COPD)/asthma/interstitial lung disease (ILD)-related infection (~ 22,730 cases and ~ 112,908 controls) were also conducted to enhance the credibility of the selected instruments and MR-based estimates. This study found that genetically predicted PD-1/PD-L1 were not significantly associated with lung cancer after adjustment for multiplicity. However, suggestive evidence was observed for the total effect of higher PD-1 with decreased lung cancer risk and the direct effect (i.e., not mediated by PD-1 and smoking) of lower PD-L1 with decreased lung cancer risk. No association between genetically predicted PD-L1 and COPD/asthma/ILD related infection was noted. Taken together, our findings suggest that interventions decreasing PD-L1 might have a role in lowering lung cancer risk.
引用
收藏
页码:3279 / 3288
页数:9
相关论文
共 195 条
[1]  
Antonia SJ(2017)Durvalumab after chemoradiotherapy in stage III non-small-cell lung cancer N Engl J Med 377 1919-1929
[2]  
Villegas A(2015)Genomic variation. Impact of regulatory variation from RNA to protein Science 347 664-667
[3]  
Daniel D(2015)Nivolumab versus docetaxel in advanced nonsquamous non-small-cell lung cancer N Engl J Med 373 1627-1639
[4]  
Vicente D(2015)Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression Int J Epidemiol 44 512-525
[5]  
Murakami S(2016)Consistent estimation in Mendelian randomization with some invalid instruments using a weighted median estimator Genet Epidemiol 40 304-314
[6]  
Hui R(2015)Nivolumab versus docetaxel in advanced squamous-cell non-small-cell lung cancer N Engl J Med 373 123-135
[7]  
Battle A(2018)Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries CA Cancer J Clin 68 394-424
[8]  
Khan Z(2013)Calculating statistical power in Mendelian randomization studies Int J Epidemiol 42 1497-1501
[9]  
Wang SH(2015)Multivariable Mendelian randomization: the use of pleiotropic genetic variants to estimate causal effects Am J Epidemiol 181 251-260
[10]  
Mitrano A(2017)Interpreting findings from Mendelian randomization using the MR-Egger method Eur J Epidemiol 32 377-389