Microrna-296-5p is differentially expressed in individuals with and without hiv-1 infection

6Citations
Citations of this article
17Readers
Mendeley users who have this article in their library.

Abstract

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.

Author supplied keywords

Cite

CITATION STYLE

APA

Cárdenas-Bedoya, J., Marquez-Pedroza, J., Morán-Moguel, M. C., Escoto-Delgadillo, M., Vázquez-Valls, E., González-Enríquez, G. V., … Torres-Mendoza, B. M. (2020). Microrna-296-5p is differentially expressed in individuals with and without hiv-1 infection. Genetics and Molecular Biology, 43(3), 1–4. https://doi.org/10.1590/1678-4685-gmb-2020-0017

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free