Integrated analysis of long non-coding RNA-microRNA-mRNA competing endogenous RNAregulatory networks in thromboangiitis obliterans
Thromboangiitis obliterans (TAO) is a non-atherosclerotic, segmental, chronic vascular inflammatory disease. Our aim was to explore the underlying mechanisms of long non-coding RNA (lncRNA)-related competing endogenous RNAs (ceRNAs) in TAO. Six blood samples were collected from patients with TAO and...
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Taylor & Francis Group
2021
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oai:doaj.org-article:71b851d29c2544cb81704338b72a781d2021-11-26T11:19:49ZIntegrated analysis of long non-coding RNA-microRNA-mRNA competing endogenous RNAregulatory networks in thromboangiitis obliterans2165-59792165-598710.1080/21655979.2021.2002497https://doaj.org/article/71b851d29c2544cb81704338b72a781d2021-11-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.2002497https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987Thromboangiitis obliterans (TAO) is a non-atherosclerotic, segmental, chronic vascular inflammatory disease. Our aim was to explore the underlying mechanisms of long non-coding RNA (lncRNA)-related competing endogenous RNAs (ceRNAs) in TAO. Six blood samples were collected from patients with TAO and healthy individuals (three for each category). Total RNA was extracted from the blood of each participant and sequenced. Differentially expressed lncRNAs (DE-lncRNAs) and miRNAs (DE-miRNAs) were screened, and ceRNA networks associated with TAO were constructed. Thereafter, the genes in the ceRNA network were subjected to functional analyses. Finally, a ceRNA relationship (lncRNA NEAT1-hsa-miR-1-3p-mRNA GNA12) was selected for further validation. Analysis revealed that 347 DE-lncRNAs (150 downregulated and 197 upregulated) and 16 DE-miRNAs (3 downregulated and 13 upregulated) were identified in TAO. Further, TAO-associated ceRNA networks, which included 219 lncRNAs, 6 miRNAs, and 53 mRNAs, were proposed and subjected to gene annotation and pathway analysis. Additionally, NEAT1 and GNA12 levels were significantly upregulated, while miR-1-3p levels were evidently downregulated in TAO patients, as compared with those in healthy controls. Dual luciferase reporter assays showed that NEAT1, miR-1-3p, and GNA12 interacted with each other. We report potential TAO-associated ceRNA regulatory networks and suggest activation of NEAT1/miR-1-3p/GNA12 signaling as a novel mechanism for TAO progression.Bo ChenYing DengBo WangZhongyi TianJindong TongBo YuWeijun ShiJingdong TangTaylor & Francis Grouparticlethromboangiitis obliteranslncrnamirnacerna networkBiotechnologyTP248.13-248.65ENBioengineered, Vol 0, Iss 0 (2021) |
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thromboangiitis obliterans lncrna mirna cerna network Biotechnology TP248.13-248.65 |
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thromboangiitis obliterans lncrna mirna cerna network Biotechnology TP248.13-248.65 Bo Chen Ying Deng Bo Wang Zhongyi Tian Jindong Tong Bo Yu Weijun Shi Jingdong Tang Integrated analysis of long non-coding RNA-microRNA-mRNA competing endogenous RNAregulatory networks in thromboangiitis obliterans |
description |
Thromboangiitis obliterans (TAO) is a non-atherosclerotic, segmental, chronic vascular inflammatory disease. Our aim was to explore the underlying mechanisms of long non-coding RNA (lncRNA)-related competing endogenous RNAs (ceRNAs) in TAO. Six blood samples were collected from patients with TAO and healthy individuals (three for each category). Total RNA was extracted from the blood of each participant and sequenced. Differentially expressed lncRNAs (DE-lncRNAs) and miRNAs (DE-miRNAs) were screened, and ceRNA networks associated with TAO were constructed. Thereafter, the genes in the ceRNA network were subjected to functional analyses. Finally, a ceRNA relationship (lncRNA NEAT1-hsa-miR-1-3p-mRNA GNA12) was selected for further validation. Analysis revealed that 347 DE-lncRNAs (150 downregulated and 197 upregulated) and 16 DE-miRNAs (3 downregulated and 13 upregulated) were identified in TAO. Further, TAO-associated ceRNA networks, which included 219 lncRNAs, 6 miRNAs, and 53 mRNAs, were proposed and subjected to gene annotation and pathway analysis. Additionally, NEAT1 and GNA12 levels were significantly upregulated, while miR-1-3p levels were evidently downregulated in TAO patients, as compared with those in healthy controls. Dual luciferase reporter assays showed that NEAT1, miR-1-3p, and GNA12 interacted with each other. We report potential TAO-associated ceRNA regulatory networks and suggest activation of NEAT1/miR-1-3p/GNA12 signaling as a novel mechanism for TAO progression. |
format |
article |
author |
Bo Chen Ying Deng Bo Wang Zhongyi Tian Jindong Tong Bo Yu Weijun Shi Jingdong Tang |
author_facet |
Bo Chen Ying Deng Bo Wang Zhongyi Tian Jindong Tong Bo Yu Weijun Shi Jingdong Tang |
author_sort |
Bo Chen |
title |
Integrated analysis of long non-coding RNA-microRNA-mRNA competing endogenous RNAregulatory networks in thromboangiitis obliterans |
title_short |
Integrated analysis of long non-coding RNA-microRNA-mRNA competing endogenous RNAregulatory networks in thromboangiitis obliterans |
title_full |
Integrated analysis of long non-coding RNA-microRNA-mRNA competing endogenous RNAregulatory networks in thromboangiitis obliterans |
title_fullStr |
Integrated analysis of long non-coding RNA-microRNA-mRNA competing endogenous RNAregulatory networks in thromboangiitis obliterans |
title_full_unstemmed |
Integrated analysis of long non-coding RNA-microRNA-mRNA competing endogenous RNAregulatory networks in thromboangiitis obliterans |
title_sort |
integrated analysis of long non-coding rna-microrna-mrna competing endogenous rnaregulatory networks in thromboangiitis obliterans |
publisher |
Taylor & Francis Group |
publishDate |
2021 |
url |
https://doaj.org/article/71b851d29c2544cb81704338b72a781d |
work_keys_str_mv |
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