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Long noncoding RNA expression profile from cryptococcal meningitis patients identifies DPY19L1p1 as a new disease marker

AIMS: LncRNAs play a vital role in the pathological and physiological process. This study aimed to explore the involvement of lncRNAs in cryptococcal meningitis. METHODS: Microarray was performed in cryptococcal meningitis patients, and then, GO and KEGG pathways were analyzed. Coexpression relation...

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Autores principales: Zhang, Lei, Fang, Wen‐Jie, Zhang, Ke‐Ming, Jiang, Wei‐Wei, Chen, Min, Liao, Wan‐Qing, Pan, Wei‐Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515894/
https://www.ncbi.nlm.nih.gov/pubmed/30767376
http://dx.doi.org/10.1111/cns.13109
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author Zhang, Lei
Fang, Wen‐Jie
Zhang, Ke‐Ming
Jiang, Wei‐Wei
Chen, Min
Liao, Wan‐Qing
Pan, Wei‐Hua
author_facet Zhang, Lei
Fang, Wen‐Jie
Zhang, Ke‐Ming
Jiang, Wei‐Wei
Chen, Min
Liao, Wan‐Qing
Pan, Wei‐Hua
author_sort Zhang, Lei
collection PubMed
description AIMS: LncRNAs play a vital role in the pathological and physiological process. This study aimed to explore the involvement of lncRNAs in cryptococcal meningitis. METHODS: Microarray was performed in cryptococcal meningitis patients, and then, GO and KEGG pathways were analyzed. Coexpression relationship between lncRNA and mRNA was explored. The expressions of the lncRNAs and mRNAs, and their changes after treatment were detected by PCR. RESULTS: A total of 325 mRNAs (201 upregulated and 124 downregulated) and 497 lncRNAs (263 upregulated and 234 downregulated) were identified. The top three enriched GO terms for the mRNAs were arachidonic acid binding, activin receptor binding, and replication fork protection complex. The top three pathways in KEGG were asthma, one carbon pool by folate, and allograft rejection. A total of 305 coexpression relationships were found between 108 lncRNAs and 87 mRNAs. LncRNA‐DPY19L1p1 was significantly increased in patients and decreased after treatment. ROC analysis revealed DPY19L1p1 was a potential diagnostic marker (AUC(ROC) = 0.9389). Furthermore, the target genes of DPY19L1p1 in cis or trans regulation were mainly involved in immune‐related pathways like the interleukin signaling pathway. CONCLUSIONS: This study analyzed the differential lncRNA profile in cryptococcal meningitis patients and revealed DPY19L1p1 could be used for treatment evaluation and disease diagnosis.
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spelling pubmed-65158942019-06-26 Long noncoding RNA expression profile from cryptococcal meningitis patients identifies DPY19L1p1 as a new disease marker Zhang, Lei Fang, Wen‐Jie Zhang, Ke‐Ming Jiang, Wei‐Wei Chen, Min Liao, Wan‐Qing Pan, Wei‐Hua CNS Neurosci Ther Original Articles AIMS: LncRNAs play a vital role in the pathological and physiological process. This study aimed to explore the involvement of lncRNAs in cryptococcal meningitis. METHODS: Microarray was performed in cryptococcal meningitis patients, and then, GO and KEGG pathways were analyzed. Coexpression relationship between lncRNA and mRNA was explored. The expressions of the lncRNAs and mRNAs, and their changes after treatment were detected by PCR. RESULTS: A total of 325 mRNAs (201 upregulated and 124 downregulated) and 497 lncRNAs (263 upregulated and 234 downregulated) were identified. The top three enriched GO terms for the mRNAs were arachidonic acid binding, activin receptor binding, and replication fork protection complex. The top three pathways in KEGG were asthma, one carbon pool by folate, and allograft rejection. A total of 305 coexpression relationships were found between 108 lncRNAs and 87 mRNAs. LncRNA‐DPY19L1p1 was significantly increased in patients and decreased after treatment. ROC analysis revealed DPY19L1p1 was a potential diagnostic marker (AUC(ROC) = 0.9389). Furthermore, the target genes of DPY19L1p1 in cis or trans regulation were mainly involved in immune‐related pathways like the interleukin signaling pathway. CONCLUSIONS: This study analyzed the differential lncRNA profile in cryptococcal meningitis patients and revealed DPY19L1p1 could be used for treatment evaluation and disease diagnosis. John Wiley and Sons Inc. 2019-02-14 /pmc/articles/PMC6515894/ /pubmed/30767376 http://dx.doi.org/10.1111/cns.13109 Text en © 2019 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Zhang, Lei
Fang, Wen‐Jie
Zhang, Ke‐Ming
Jiang, Wei‐Wei
Chen, Min
Liao, Wan‐Qing
Pan, Wei‐Hua
Long noncoding RNA expression profile from cryptococcal meningitis patients identifies DPY19L1p1 as a new disease marker
title Long noncoding RNA expression profile from cryptococcal meningitis patients identifies DPY19L1p1 as a new disease marker
title_full Long noncoding RNA expression profile from cryptococcal meningitis patients identifies DPY19L1p1 as a new disease marker
title_fullStr Long noncoding RNA expression profile from cryptococcal meningitis patients identifies DPY19L1p1 as a new disease marker
title_full_unstemmed Long noncoding RNA expression profile from cryptococcal meningitis patients identifies DPY19L1p1 as a new disease marker
title_short Long noncoding RNA expression profile from cryptococcal meningitis patients identifies DPY19L1p1 as a new disease marker
title_sort long noncoding rna expression profile from cryptococcal meningitis patients identifies dpy19l1p1 as a new disease marker
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515894/
https://www.ncbi.nlm.nih.gov/pubmed/30767376
http://dx.doi.org/10.1111/cns.13109
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