Mendelian randomization study of interleukin (IL)-1 family and lung cancer

Abstract The role of interleukin (IL)-1 family members/receptors in lung cancer remains uncertain due to the susceptibility of observed associations to confounding. We appraised the association of IL-1 family members/receptors with lung cancer and its subtypes [lung adenocarcinoma (LUAD) and squamou...

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Main Authors: Zhao Yang, C. Mary Schooling, Man Ki Kwok
Format: Article
Language:English
Published: Nature Publishing Group 2021-09-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-97099-5
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spelling doaj-6a230508876e4b669955f93eca42a5822021-09-05T11:33:28ZengNature Publishing GroupScientific Reports2045-23222021-09-0111111110.1038/s41598-021-97099-5Mendelian randomization study of interleukin (IL)-1 family and lung cancerZhao Yang0C. Mary Schooling1Man Ki Kwok2School of Public Health, Li Ka Shing, Faculty of Medicine, The University of Hong KongSchool of Public Health, Li Ka Shing, Faculty of Medicine, The University of Hong KongSchool of Public Health, Li Ka Shing, Faculty of Medicine, The University of Hong KongAbstract The role of interleukin (IL)-1 family members/receptors in lung cancer remains uncertain due to the susceptibility of observed associations to confounding. We appraised the association of IL-1 family members/receptors with lung cancer and its subtypes [lung adenocarcinoma (LUAD) and squamous cell lung cancer (LUSC)] using two-sample Mendelian randomization. This study found that no IL-1 family members/receptors were significantly associated with lung cancer and its subtypes risk after correction for multiple testing. However, suggestive total effects of increased risk were noted for genetically predicted IL-1Racp with lung cancer (P = 0.006), IL-1α with LUAD (P = 0.027), and IL-1Racp with LUSC (P = 0.008). Suggestive direct effects were also noted for IL-1β, IL-1Ra, IL-36γ with lung cancer, IL-1α/β, IL-1Ra with LUAD, and IL-1β, IL-18BP with LUSC, after adjusting for genetically predicted effects of other IL-1 family members/receptors. Taken together, our findings suggest that interventions decreasing IL-1Racp might protect against lung cancer, perhaps via IL-1α/β or IL-1Ra.https://doi.org/10.1038/s41598-021-97099-5
collection DOAJ
language English
format Article
sources DOAJ
author Zhao Yang
C. Mary Schooling
Man Ki Kwok
spellingShingle Zhao Yang
C. Mary Schooling
Man Ki Kwok
Mendelian randomization study of interleukin (IL)-1 family and lung cancer
Scientific Reports
author_facet Zhao Yang
C. Mary Schooling
Man Ki Kwok
author_sort Zhao Yang
title Mendelian randomization study of interleukin (IL)-1 family and lung cancer
title_short Mendelian randomization study of interleukin (IL)-1 family and lung cancer
title_full Mendelian randomization study of interleukin (IL)-1 family and lung cancer
title_fullStr Mendelian randomization study of interleukin (IL)-1 family and lung cancer
title_full_unstemmed Mendelian randomization study of interleukin (IL)-1 family and lung cancer
title_sort mendelian randomization study of interleukin (il)-1 family and lung cancer
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-09-01
description Abstract The role of interleukin (IL)-1 family members/receptors in lung cancer remains uncertain due to the susceptibility of observed associations to confounding. We appraised the association of IL-1 family members/receptors with lung cancer and its subtypes [lung adenocarcinoma (LUAD) and squamous cell lung cancer (LUSC)] using two-sample Mendelian randomization. This study found that no IL-1 family members/receptors were significantly associated with lung cancer and its subtypes risk after correction for multiple testing. However, suggestive total effects of increased risk were noted for genetically predicted IL-1Racp with lung cancer (P = 0.006), IL-1α with LUAD (P = 0.027), and IL-1Racp with LUSC (P = 0.008). Suggestive direct effects were also noted for IL-1β, IL-1Ra, IL-36γ with lung cancer, IL-1α/β, IL-1Ra with LUAD, and IL-1β, IL-18BP with LUSC, after adjusting for genetically predicted effects of other IL-1 family members/receptors. Taken together, our findings suggest that interventions decreasing IL-1Racp might protect against lung cancer, perhaps via IL-1α/β or IL-1Ra.
url https://doi.org/10.1038/s41598-021-97099-5
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