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MicroRNA-296-5p is differentially expressed in individuals with and without HIV-1 infection

MicroRNAs are considered as potential biomarkers, agents, or therapeutic targets; few studies have addressed the expression of miRNAs in treatment-naïve patients infected with HIV-1. The aim of this study was to assess plasma relative circulating miRNA expression profiles in treatment-naïve Mexican...

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Autores principales: Cárdenas-Bedoya, Jhonathan, Marquez-Pedroza, Jazmin, Morán-Moguel, María Cristina, Escoto-Delgadillo, Martha, Vázquez-Valls, Eduardo, González-Enríquez, Gracia Viviana, Pérez-Ríos, Alma Minerva, Torres-Mendoza, Blanca Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315763/
https://www.ncbi.nlm.nih.gov/pubmed/32584920
http://dx.doi.org/10.1590/1678-4685-GMB-2020-0017
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author Cárdenas-Bedoya, Jhonathan
Marquez-Pedroza, Jazmin
Morán-Moguel, María Cristina
Escoto-Delgadillo, Martha
Vázquez-Valls, Eduardo
González-Enríquez, Gracia Viviana
Pérez-Ríos, Alma Minerva
Torres-Mendoza, Blanca Miriam
author_facet Cárdenas-Bedoya, Jhonathan
Marquez-Pedroza, Jazmin
Morán-Moguel, María Cristina
Escoto-Delgadillo, Martha
Vázquez-Valls, Eduardo
González-Enríquez, Gracia Viviana
Pérez-Ríos, Alma Minerva
Torres-Mendoza, Blanca Miriam
author_sort Cárdenas-Bedoya, Jhonathan
collection PubMed
description MicroRNAs are considered as potential biomarkers, agents, or therapeutic targets; few studies have addressed the expression of miRNAs in treatment-naïve patients infected with HIV-1. The aim of this study was to assess plasma relative circulating miRNA expression profiles in treatment-naïve Mexican patients with HIV/AIDS and healthy individuals using a commercial array. A low CD4+ T cell count and high viral load were found in all patients. Decreased relative miRNA-296-5p expression was observed in patients; moreover, this was the only miRNA that showed differences between the two groups. Thus, we measured the absolute expression of miR-296-5p by qPCR, confirming the result with statistically significant differences (P < 0.05). There is evidence that miR-296-5p regulates the expression of the PIN1 gene, which encodes the peptidylprolyl Cis/Trans isomerase NIMA-Interacting-1, that is involved in different stages of the biological cycle of HIV-1, this relationship is corroborated by bioinformatics analysis and ELISA assay was used to measure plasma levels of PIN1. The decreased expression of miR-296-5p found in naïve patients with HIV infection suggests a regulatory activity of this miRNA on virus replication, making it a potential therapeutic agent against HIV. Finally, miR-296-5p could be inhibiting the virus transcription by regulating genes different than PIN1.
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spelling pubmed-73157632020-07-06 MicroRNA-296-5p is differentially expressed in individuals with and without HIV-1 infection Cárdenas-Bedoya, Jhonathan Marquez-Pedroza, Jazmin Morán-Moguel, María Cristina Escoto-Delgadillo, Martha Vázquez-Valls, Eduardo González-Enríquez, Gracia Viviana Pérez-Ríos, Alma Minerva Torres-Mendoza, Blanca Miriam Genet Mol Biol Human and Medical Genetics MicroRNAs are considered as potential biomarkers, agents, or therapeutic targets; few studies have addressed the expression of miRNAs in treatment-naïve patients infected with HIV-1. The aim of this study was to assess plasma relative circulating miRNA expression profiles in treatment-naïve Mexican patients with HIV/AIDS and healthy individuals using a commercial array. A low CD4+ T cell count and high viral load were found in all patients. Decreased relative miRNA-296-5p expression was observed in patients; moreover, this was the only miRNA that showed differences between the two groups. Thus, we measured the absolute expression of miR-296-5p by qPCR, confirming the result with statistically significant differences (P < 0.05). There is evidence that miR-296-5p regulates the expression of the PIN1 gene, which encodes the peptidylprolyl Cis/Trans isomerase NIMA-Interacting-1, that is involved in different stages of the biological cycle of HIV-1, this relationship is corroborated by bioinformatics analysis and ELISA assay was used to measure plasma levels of PIN1. The decreased expression of miR-296-5p found in naïve patients with HIV infection suggests a regulatory activity of this miRNA on virus replication, making it a potential therapeutic agent against HIV. Finally, miR-296-5p could be inhibiting the virus transcription by regulating genes different than PIN1. Sociedade Brasileira de Genética 2020-06-22 /pmc/articles/PMC7315763/ /pubmed/32584920 http://dx.doi.org/10.1590/1678-4685-GMB-2020-0017 Text en Copyright © 2020, Sociedade Brasileira de Genética. https://creativecommons.org/licenses/by/4.0/ License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited.
spellingShingle Human and Medical Genetics
Cárdenas-Bedoya, Jhonathan
Marquez-Pedroza, Jazmin
Morán-Moguel, María Cristina
Escoto-Delgadillo, Martha
Vázquez-Valls, Eduardo
González-Enríquez, Gracia Viviana
Pérez-Ríos, Alma Minerva
Torres-Mendoza, Blanca Miriam
MicroRNA-296-5p is differentially expressed in individuals with and without HIV-1 infection
title MicroRNA-296-5p is differentially expressed in individuals with and without HIV-1 infection
title_full MicroRNA-296-5p is differentially expressed in individuals with and without HIV-1 infection
title_fullStr MicroRNA-296-5p is differentially expressed in individuals with and without HIV-1 infection
title_full_unstemmed MicroRNA-296-5p is differentially expressed in individuals with and without HIV-1 infection
title_short MicroRNA-296-5p is differentially expressed in individuals with and without HIV-1 infection
title_sort microrna-296-5p is differentially expressed in individuals with and without hiv-1 infection
topic Human and Medical Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315763/
https://www.ncbi.nlm.nih.gov/pubmed/32584920
http://dx.doi.org/10.1590/1678-4685-GMB-2020-0017
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