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Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals
Liver disease is one of the main contributors to the increased levels of morbidity and mortality seen in the HIV-1-infected, ART-treated population. Circulating miRNAs, particularly those located inside extracellular vesicles, are seen as promising biomarkers for a number of human disease conditions...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589757/ https://www.ncbi.nlm.nih.gov/pubmed/28883647 http://dx.doi.org/10.1038/s41598-017-11405-8 |
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author | Murray, Daniel D. Suzuki, Kazuo Law, Matthew Trebicka, Jonel Neuhaus Nordwall, Jacquie Johnson, Margaret Vjecha, Michael J. Kelleher, Anthony D. Emery, Sean |
author_facet | Murray, Daniel D. Suzuki, Kazuo Law, Matthew Trebicka, Jonel Neuhaus Nordwall, Jacquie Johnson, Margaret Vjecha, Michael J. Kelleher, Anthony D. Emery, Sean |
author_sort | Murray, Daniel D. |
collection | PubMed |
description | Liver disease is one of the main contributors to the increased levels of morbidity and mortality seen in the HIV-1-infected, ART-treated population. Circulating miRNAs, particularly those located inside extracellular vesicles, are seen as promising biomarkers for a number of human disease conditions, including liver-related diseases. Here, we show that serum levels of miR-122 and miR-200a are greater in HIV/HCV co-infected individuals compared to HIV-1 mono-infected individuals. We also show that miR-122 and miR-200a are elevated in ART-treated, HIV-1-infected individuals prior to the development of fatal liver disease, suggesting that these miRNA may have some potential clinical utility as biomarkers. While this study is hypothesis generating, it shows clearly that both miR-122 and miR-200a are promising novel biomarkers for liver disease in the ART-treated, HIV-1-infected population. |
format | Online Article Text |
id | pubmed-5589757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55897572017-09-13 Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals Murray, Daniel D. Suzuki, Kazuo Law, Matthew Trebicka, Jonel Neuhaus Nordwall, Jacquie Johnson, Margaret Vjecha, Michael J. Kelleher, Anthony D. Emery, Sean Sci Rep Article Liver disease is one of the main contributors to the increased levels of morbidity and mortality seen in the HIV-1-infected, ART-treated population. Circulating miRNAs, particularly those located inside extracellular vesicles, are seen as promising biomarkers for a number of human disease conditions, including liver-related diseases. Here, we show that serum levels of miR-122 and miR-200a are greater in HIV/HCV co-infected individuals compared to HIV-1 mono-infected individuals. We also show that miR-122 and miR-200a are elevated in ART-treated, HIV-1-infected individuals prior to the development of fatal liver disease, suggesting that these miRNA may have some potential clinical utility as biomarkers. While this study is hypothesis generating, it shows clearly that both miR-122 and miR-200a are promising novel biomarkers for liver disease in the ART-treated, HIV-1-infected population. Nature Publishing Group UK 2017-09-07 /pmc/articles/PMC5589757/ /pubmed/28883647 http://dx.doi.org/10.1038/s41598-017-11405-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Murray, Daniel D. Suzuki, Kazuo Law, Matthew Trebicka, Jonel Neuhaus Nordwall, Jacquie Johnson, Margaret Vjecha, Michael J. Kelleher, Anthony D. Emery, Sean Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals |
title | Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals |
title_full | Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals |
title_fullStr | Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals |
title_full_unstemmed | Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals |
title_short | Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals |
title_sort | circulating mir-122 and mir-200a as biomarkers for fatal liver disease in art-treated, hiv-1-infected individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589757/ https://www.ncbi.nlm.nih.gov/pubmed/28883647 http://dx.doi.org/10.1038/s41598-017-11405-8 |
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