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Evidence based on Mendelian randomization: Causal relationship between mitochondrial biological function and lung cancer and its subtypes

OBJECTIVE: This study aimed to investigate the causal relationship between mitochondrial biological function and lung cancer, including its subtypes, via MR. METHODS: SNPs significantly associated with lung cancer and its subtypes were employed as instrumental variables. MR-Egger regression, simple...

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Autores principales: Zhu, Kangle, Shi, Jingwei, Yang, Rusong, Zhou, Chu, Liu, Zhengcheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685044/
https://www.ncbi.nlm.nih.gov/pubmed/37976568
http://dx.doi.org/10.1016/j.neo.2023.100950
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author Zhu, Kangle
Shi, Jingwei
Yang, Rusong
Zhou, Chu
Liu, Zhengcheng
author_facet Zhu, Kangle
Shi, Jingwei
Yang, Rusong
Zhou, Chu
Liu, Zhengcheng
author_sort Zhu, Kangle
collection PubMed
description OBJECTIVE: This study aimed to investigate the causal relationship between mitochondrial biological function and lung cancer, including its subtypes, via MR. METHODS: SNPs significantly associated with lung cancer and its subtypes were employed as instrumental variables. MR-Egger regression, simple mode, weighted mode, simple median, and weighted median, were utilized to determine the causal relationship between the exposure factor and the occurrence of lung cancer and its subtypes. RESULTS: NADH dehydrogenase (ubiquinone) flavoprotein 2 and transmembrane protein 70 were found to have a causal relationship with lung adenocarcinoma, acting as protective factors. The causal relationship between mitochondrial import inner membrane translocase subunit and NADH dehydrogenase (ubiquinone) iron-sulfur protein 4 and small-cell lung cancer was established as a risk factor. NADH dehydrogenase (ubiquinone) 1 beta subcomplex subunit 8 exhibited a causal relationship with small-cell lung cancer, acting as a protective factor. Furthermore, NAD-dependent protein deacylase sirtuin-5 was causally linked to lung squamous cell carcinoma, serving as a protective factor. A funnel plot demonstrated the symmetrical distribution of the SNPs. Thew pleiotroy test (P > 0.05) and "leave-one-out" test validated the relative stability of the results. CONCLUSION: This study established a causal relationship between mitochondrial biological function and lung cancer, including its subtypes.
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spelling pubmed-106850442023-11-30 Evidence based on Mendelian randomization: Causal relationship between mitochondrial biological function and lung cancer and its subtypes Zhu, Kangle Shi, Jingwei Yang, Rusong Zhou, Chu Liu, Zhengcheng Neoplasia Original article OBJECTIVE: This study aimed to investigate the causal relationship between mitochondrial biological function and lung cancer, including its subtypes, via MR. METHODS: SNPs significantly associated with lung cancer and its subtypes were employed as instrumental variables. MR-Egger regression, simple mode, weighted mode, simple median, and weighted median, were utilized to determine the causal relationship between the exposure factor and the occurrence of lung cancer and its subtypes. RESULTS: NADH dehydrogenase (ubiquinone) flavoprotein 2 and transmembrane protein 70 were found to have a causal relationship with lung adenocarcinoma, acting as protective factors. The causal relationship between mitochondrial import inner membrane translocase subunit and NADH dehydrogenase (ubiquinone) iron-sulfur protein 4 and small-cell lung cancer was established as a risk factor. NADH dehydrogenase (ubiquinone) 1 beta subcomplex subunit 8 exhibited a causal relationship with small-cell lung cancer, acting as a protective factor. Furthermore, NAD-dependent protein deacylase sirtuin-5 was causally linked to lung squamous cell carcinoma, serving as a protective factor. A funnel plot demonstrated the symmetrical distribution of the SNPs. Thew pleiotroy test (P > 0.05) and "leave-one-out" test validated the relative stability of the results. CONCLUSION: This study established a causal relationship between mitochondrial biological function and lung cancer, including its subtypes. Neoplasia Press 2023-11-16 /pmc/articles/PMC10685044/ /pubmed/37976568 http://dx.doi.org/10.1016/j.neo.2023.100950 Text en © 2023 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
Zhu, Kangle
Shi, Jingwei
Yang, Rusong
Zhou, Chu
Liu, Zhengcheng
Evidence based on Mendelian randomization: Causal relationship between mitochondrial biological function and lung cancer and its subtypes
title Evidence based on Mendelian randomization: Causal relationship between mitochondrial biological function and lung cancer and its subtypes
title_full Evidence based on Mendelian randomization: Causal relationship between mitochondrial biological function and lung cancer and its subtypes
title_fullStr Evidence based on Mendelian randomization: Causal relationship between mitochondrial biological function and lung cancer and its subtypes
title_full_unstemmed Evidence based on Mendelian randomization: Causal relationship between mitochondrial biological function and lung cancer and its subtypes
title_short Evidence based on Mendelian randomization: Causal relationship between mitochondrial biological function and lung cancer and its subtypes
title_sort evidence based on mendelian randomization: causal relationship between mitochondrial biological function and lung cancer and its subtypes
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685044/
https://www.ncbi.nlm.nih.gov/pubmed/37976568
http://dx.doi.org/10.1016/j.neo.2023.100950
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