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Identification of Circulating miR-22-3p and miR-93-5p as Stable Endogenous Control in Tuberculosis Study

The diagnosis and prognosis of tuberculosis remains challenging and necessitates the development of a new test that can accurately diagnose and monitor treatment responses. In this regard, miRNA is becoming a potential diagnostic and prognostic biomarker which differentiates treatment respondents fr...

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Detalles Bibliográficos
Autores principales: Korma, Workneh, Mihret, Adane, Tarekegn, Azeb, Chang, Yunhee, Hwang, Dasom, Tessema, Tesfaye Sisay, Lee, Hyeyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690830/
https://www.ncbi.nlm.nih.gov/pubmed/33114169
http://dx.doi.org/10.3390/diagnostics10110868
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author Korma, Workneh
Mihret, Adane
Tarekegn, Azeb
Chang, Yunhee
Hwang, Dasom
Tessema, Tesfaye Sisay
Lee, Hyeyoung
author_facet Korma, Workneh
Mihret, Adane
Tarekegn, Azeb
Chang, Yunhee
Hwang, Dasom
Tessema, Tesfaye Sisay
Lee, Hyeyoung
author_sort Korma, Workneh
collection PubMed
description The diagnosis and prognosis of tuberculosis remains challenging and necessitates the development of a new test that can accurately diagnose and monitor treatment responses. In this regard, miRNA is becoming a potential diagnostic and prognostic biomarker which differentiates treatment respondents from non-respondents for various non-infectious and infectious diseases, including tuberculosis. The concentration of miRNAs varies based on cell type, disease, and site of infection, implicating that selection of an optimal reference gene is crucial, and determines the quantification of transcript level and biological interpretation of the data. Thus, the study evaluated the stability and expression level of five candidate miRNAs (let-7i-5p, let-7a-5p, miRNA-16-5p, miRNA-22-3p and miRNA-93-5p), including U6 Small Nuclear RNA (RNU6B) to normalize circulating miRNAs in the plasma of 68 participants (26 healthy controls, 23 latent, and 19 pulmonary tuberculosis infected) recruited from four health centers and three hospitals in Addis Ababa, Ethiopia. The expression levels of miRNAs isolated from plasma of culture confirmed newly diagnosed pulmonary tuberculosis patients were compared with latently infected and non-infected healthy controls. The qPCR data were analyzed using four independent statistical tools: Best Keeper, Genorm, Normfinder and comparative delta-Ct methods, and the data showed that miRNA-22-3p and miRNA-93-5p were suitable plasma reference miRNAs in a tuberculosis study.
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spelling pubmed-76908302020-11-27 Identification of Circulating miR-22-3p and miR-93-5p as Stable Endogenous Control in Tuberculosis Study Korma, Workneh Mihret, Adane Tarekegn, Azeb Chang, Yunhee Hwang, Dasom Tessema, Tesfaye Sisay Lee, Hyeyoung Diagnostics (Basel) Article The diagnosis and prognosis of tuberculosis remains challenging and necessitates the development of a new test that can accurately diagnose and monitor treatment responses. In this regard, miRNA is becoming a potential diagnostic and prognostic biomarker which differentiates treatment respondents from non-respondents for various non-infectious and infectious diseases, including tuberculosis. The concentration of miRNAs varies based on cell type, disease, and site of infection, implicating that selection of an optimal reference gene is crucial, and determines the quantification of transcript level and biological interpretation of the data. Thus, the study evaluated the stability and expression level of five candidate miRNAs (let-7i-5p, let-7a-5p, miRNA-16-5p, miRNA-22-3p and miRNA-93-5p), including U6 Small Nuclear RNA (RNU6B) to normalize circulating miRNAs in the plasma of 68 participants (26 healthy controls, 23 latent, and 19 pulmonary tuberculosis infected) recruited from four health centers and three hospitals in Addis Ababa, Ethiopia. The expression levels of miRNAs isolated from plasma of culture confirmed newly diagnosed pulmonary tuberculosis patients were compared with latently infected and non-infected healthy controls. The qPCR data were analyzed using four independent statistical tools: Best Keeper, Genorm, Normfinder and comparative delta-Ct methods, and the data showed that miRNA-22-3p and miRNA-93-5p were suitable plasma reference miRNAs in a tuberculosis study. MDPI 2020-10-23 /pmc/articles/PMC7690830/ /pubmed/33114169 http://dx.doi.org/10.3390/diagnostics10110868 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Korma, Workneh
Mihret, Adane
Tarekegn, Azeb
Chang, Yunhee
Hwang, Dasom
Tessema, Tesfaye Sisay
Lee, Hyeyoung
Identification of Circulating miR-22-3p and miR-93-5p as Stable Endogenous Control in Tuberculosis Study
title Identification of Circulating miR-22-3p and miR-93-5p as Stable Endogenous Control in Tuberculosis Study
title_full Identification of Circulating miR-22-3p and miR-93-5p as Stable Endogenous Control in Tuberculosis Study
title_fullStr Identification of Circulating miR-22-3p and miR-93-5p as Stable Endogenous Control in Tuberculosis Study
title_full_unstemmed Identification of Circulating miR-22-3p and miR-93-5p as Stable Endogenous Control in Tuberculosis Study
title_short Identification of Circulating miR-22-3p and miR-93-5p as Stable Endogenous Control in Tuberculosis Study
title_sort identification of circulating mir-22-3p and mir-93-5p as stable endogenous control in tuberculosis study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690830/
https://www.ncbi.nlm.nih.gov/pubmed/33114169
http://dx.doi.org/10.3390/diagnostics10110868
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