Identification of a Competing Endogenous RNA Network Related to Immune Signature in Lung Adenocarcinoma

BackgroundThe establishment of immunotherapy has led to a new era in oncotherapy. But the signature of immune-related genes (IRGs) in LUAD remains to be elucidated. Here we use integrated analysis to identify IRGs roles in immune signature and detect their relationship with competing endogenous RNA...

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Main Authors: Ting Zhu, Yong Yu, Jun Liu, Kaiming Ren
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.665555/full
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spelling doaj-4710f99fcd904f2bb3dd0c77c75bebb72021-06-03T05:26:37ZengFrontiers Media S.A.Frontiers in Genetics1664-80212021-06-011210.3389/fgene.2021.665555665555Identification of a Competing Endogenous RNA Network Related to Immune Signature in Lung AdenocarcinomaTing Zhu0Yong Yu1Jun Liu2Kaiming Ren3Shengjing Hospital of China Medical University, Shenyang, ChinaShengjing Hospital of China Medical University, Shenyang, ChinaDepartment of Thoracic Surgery, Shengjing Hospital of China Medical University, Shenyang, ChinaDepartment of Thoracic Surgery, Shengjing Hospital of China Medical University, Shenyang, ChinaBackgroundThe establishment of immunotherapy has led to a new era in oncotherapy. But the signature of immune-related genes (IRGs) in LUAD remains to be elucidated. Here we use integrated analysis to identify IRGs roles in immune signature and detect their relationship with competing endogenous RNA (ceRNA) networks in LUAD progression.MethodsBy analyzing the RNA-seq data from different platforms, we recognized the differentially expressed genes (DEGs) of each platform and screened out the top 20 hub IRGs related to immune responses. Then, we applied the CIBERSORT algorithm to explore the landscape of tumor-infiltrating immune cells (TILs) in LUAD and their connection with hub genes. Next, we predicted and validated the upstream miRNAs and lncRNAs according to their expression and prognostic roles. Finally, we constructed and validated an immune-related ceRNA network by co-expression analysis.ResultsA total of 71 IRGs were identified among 248 DEGs, which play key roles in immune responses. CIBERSORT analysis showed that six hub genes were closely related to TILs, such as SPP1 and naive B cells (R = −0.17), TEK and resting mast cells (R = 0.37). Stepwise prediction and validation from mRNA to lncRNA, including 6 hub genes, 5 miRNAs, and 9 lncRNAs, were applied to construct a ceRNA network. Ultimately, we confirmed the TMPO-AS1/miR-126-5p/SPP1 and CARD8-AS1/miR-21-5p/TEK as immune-related ceRNA networks in LUAD progression.ConclusionWe elucidated two immune-related ceRNA networks in LUAD progression, which can be considered as immunotherapy targets for this disease.https://www.frontiersin.org/articles/10.3389/fgene.2021.665555/fullintegrated analysislung adenocarcinomaceRNAoverall survivaltumor infiltrating immune cells
collection DOAJ
language English
format Article
sources DOAJ
author Ting Zhu
Yong Yu
Jun Liu
Kaiming Ren
spellingShingle Ting Zhu
Yong Yu
Jun Liu
Kaiming Ren
Identification of a Competing Endogenous RNA Network Related to Immune Signature in Lung Adenocarcinoma
Frontiers in Genetics
integrated analysis
lung adenocarcinoma
ceRNA
overall survival
tumor infiltrating immune cells
author_facet Ting Zhu
Yong Yu
Jun Liu
Kaiming Ren
author_sort Ting Zhu
title Identification of a Competing Endogenous RNA Network Related to Immune Signature in Lung Adenocarcinoma
title_short Identification of a Competing Endogenous RNA Network Related to Immune Signature in Lung Adenocarcinoma
title_full Identification of a Competing Endogenous RNA Network Related to Immune Signature in Lung Adenocarcinoma
title_fullStr Identification of a Competing Endogenous RNA Network Related to Immune Signature in Lung Adenocarcinoma
title_full_unstemmed Identification of a Competing Endogenous RNA Network Related to Immune Signature in Lung Adenocarcinoma
title_sort identification of a competing endogenous rna network related to immune signature in lung adenocarcinoma
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2021-06-01
description BackgroundThe establishment of immunotherapy has led to a new era in oncotherapy. But the signature of immune-related genes (IRGs) in LUAD remains to be elucidated. Here we use integrated analysis to identify IRGs roles in immune signature and detect their relationship with competing endogenous RNA (ceRNA) networks in LUAD progression.MethodsBy analyzing the RNA-seq data from different platforms, we recognized the differentially expressed genes (DEGs) of each platform and screened out the top 20 hub IRGs related to immune responses. Then, we applied the CIBERSORT algorithm to explore the landscape of tumor-infiltrating immune cells (TILs) in LUAD and their connection with hub genes. Next, we predicted and validated the upstream miRNAs and lncRNAs according to their expression and prognostic roles. Finally, we constructed and validated an immune-related ceRNA network by co-expression analysis.ResultsA total of 71 IRGs were identified among 248 DEGs, which play key roles in immune responses. CIBERSORT analysis showed that six hub genes were closely related to TILs, such as SPP1 and naive B cells (R = −0.17), TEK and resting mast cells (R = 0.37). Stepwise prediction and validation from mRNA to lncRNA, including 6 hub genes, 5 miRNAs, and 9 lncRNAs, were applied to construct a ceRNA network. Ultimately, we confirmed the TMPO-AS1/miR-126-5p/SPP1 and CARD8-AS1/miR-21-5p/TEK as immune-related ceRNA networks in LUAD progression.ConclusionWe elucidated two immune-related ceRNA networks in LUAD progression, which can be considered as immunotherapy targets for this disease.
topic integrated analysis
lung adenocarcinoma
ceRNA
overall survival
tumor infiltrating immune cells
url https://www.frontiersin.org/articles/10.3389/fgene.2021.665555/full
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AT yongyu identificationofacompetingendogenousrnanetworkrelatedtoimmunesignatureinlungadenocarcinoma
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AT kaimingren identificationofacompetingendogenousrnanetworkrelatedtoimmunesignatureinlungadenocarcinoma
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