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;
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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.
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页码:3279 / 3288
页数:9
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共 195 条
[31]  
Poddubskaya E(2017)Genetic epidemiology and Mendelian randomization for informing disease therapeutics: conceptual and methodological challenges PLoS Genet 394 1929-1833
[32]  
Bray F(2019)Durvalumab plus platinum-etoposide versus platinum-etoposide in first-line treatment of extensive-stage small-cell lung cancer (CASPIAN): a randomised, controlled, open-label, phase 3 trial Lancet 33 1974-1215
[33]  
Ferlay J(2015)Immune checkpoint blockade in cancer therapy J Clin Oncol 375 1823-2301
[34]  
Soerjomataram I(2016)Pembrolizumab versus chemotherapy for PD-L1-positive non-small-cell lung cancer N Engl J Med 35 1209-79
[35]  
Siegel RL(2010)Infection as a comorbidity of COPD Eur Respir J 7 e27857v1-1877
[36]  
Torre LA(2019)STROBE-MR: Guidelines for strengthening the reporting of Mendelian randomization studies. PeerJ Preprints 378 2288-5399
[37]  
Jemal A(2018)Atezolizumab for first-line treatment of metastatic nonsquamous NSCLC N Engl J Med 558 73-741
[38]  
Brion MJ(2018)Genomic atlas of the human plasma proteome Nature 14 1867-1131
[39]  
Shakhbazov K(2019)Effect of PD-1 inhibitor on exhaled nitric oxide and pulmonary function in non-small cell lung cancer patients with and without COPD Int J Chron Obstruct Pulmon Dis 71 5393-undefined
[40]  
Visscher PM(2011)IL-18 induces PD-1-dependent immunosuppression in cancer Cancer Res 46 736-undefined