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Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma

There are associations between DNA methylation and the expression of long non-coding RNA (lncRNA), also known as lncRNA expression quantitative trait methylations (lnc-eQTMs). Lnc-eQTMs may induce a wide range of carcinogenesis pathways. However, lnc-eQTMs have not been globally identified and studi...

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Autores principales: Wu, Xiaohong, Gao, Yue, Bu, Jianlong, Deng, Lin, Zhang, Pinyi, Chi, Meng, Jiang, Lihua, Shi, Xiaoding, Ning, Shangwei, Wang, Guonian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756030/
https://www.ncbi.nlm.nih.gov/pubmed/33362860
http://dx.doi.org/10.3389/fgene.2020.602035
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author Wu, Xiaohong
Gao, Yue
Bu, Jianlong
Deng, Lin
Zhang, Pinyi
Chi, Meng
Jiang, Lihua
Shi, Xiaoding
Ning, Shangwei
Wang, Guonian
author_facet Wu, Xiaohong
Gao, Yue
Bu, Jianlong
Deng, Lin
Zhang, Pinyi
Chi, Meng
Jiang, Lihua
Shi, Xiaoding
Ning, Shangwei
Wang, Guonian
author_sort Wu, Xiaohong
collection PubMed
description There are associations between DNA methylation and the expression of long non-coding RNA (lncRNA), also known as lncRNA expression quantitative trait methylations (lnc-eQTMs). Lnc-eQTMs may induce a wide range of carcinogenesis pathways. However, lnc-eQTMs have not been globally identified and studied, and their roles in lung adenocarcinoma (LUAD) and lung squamous carcinoma (LUSC) are largely unknown. In the present study, we identified some differential methylation sites located in genes of long intergenic non-coding RNAs (lincRNAs) and other types of lncRNAs in LUAD and LUSC. An integrated pipeline was established to construct two global cancer-specific regulatory networks of lnc-eQTMs in LUAD and LUSC. The associations between eQTMs showed common and specific features between LUAD and LUSC. Some lnc-eQTMs were also related with survival in LUAD- and LUSC-specific regulatory networks. Lnc-eQTMs were associated with cancer-related functions, such as lung epithelium development and vasculogenesis by functional analysis. Drug repurposing analysis revealed that these lnc-eQTMs may mediate the effects of some anesthesia-related drugs in LUAD and LUSC. In summary, the present study elucidates the roles of lnc-eQTMs in LUAD and LUSC, which could improve our understanding of lung cancer pathogenesis and facilitate treatment.
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spelling pubmed-77560302020-12-24 Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma Wu, Xiaohong Gao, Yue Bu, Jianlong Deng, Lin Zhang, Pinyi Chi, Meng Jiang, Lihua Shi, Xiaoding Ning, Shangwei Wang, Guonian Front Genet Genetics There are associations between DNA methylation and the expression of long non-coding RNA (lncRNA), also known as lncRNA expression quantitative trait methylations (lnc-eQTMs). Lnc-eQTMs may induce a wide range of carcinogenesis pathways. However, lnc-eQTMs have not been globally identified and studied, and their roles in lung adenocarcinoma (LUAD) and lung squamous carcinoma (LUSC) are largely unknown. In the present study, we identified some differential methylation sites located in genes of long intergenic non-coding RNAs (lincRNAs) and other types of lncRNAs in LUAD and LUSC. An integrated pipeline was established to construct two global cancer-specific regulatory networks of lnc-eQTMs in LUAD and LUSC. The associations between eQTMs showed common and specific features between LUAD and LUSC. Some lnc-eQTMs were also related with survival in LUAD- and LUSC-specific regulatory networks. Lnc-eQTMs were associated with cancer-related functions, such as lung epithelium development and vasculogenesis by functional analysis. Drug repurposing analysis revealed that these lnc-eQTMs may mediate the effects of some anesthesia-related drugs in LUAD and LUSC. In summary, the present study elucidates the roles of lnc-eQTMs in LUAD and LUSC, which could improve our understanding of lung cancer pathogenesis and facilitate treatment. Frontiers Media S.A. 2020-12-09 /pmc/articles/PMC7756030/ /pubmed/33362860 http://dx.doi.org/10.3389/fgene.2020.602035 Text en Copyright © 2020 Wu, Gao, Bu, Deng, Zhang, Chi, Jiang, Shi, Ning and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Wu, Xiaohong
Gao, Yue
Bu, Jianlong
Deng, Lin
Zhang, Pinyi
Chi, Meng
Jiang, Lihua
Shi, Xiaoding
Ning, Shangwei
Wang, Guonian
Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma
title Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma
title_full Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma
title_fullStr Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma
title_full_unstemmed Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma
title_short Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma
title_sort identification of potential long non-coding rna expression quantitative trait methylations in lung adenocarcinoma and lung squamous carcinoma
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756030/
https://www.ncbi.nlm.nih.gov/pubmed/33362860
http://dx.doi.org/10.3389/fgene.2020.602035
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