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Systems Studies Uncover miR-146a as a Target in Leishmania major Infection Model

[Image: see text] Leishmaniasis, the second most neglected tropical disease, has been reported to affect approximately 12 million people worldwide. The causative protozoan parasite Leishmania has shown drug resistance to available chemotherapies, owing to which we need to look for better approaches...

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Autores principales: Nimsarkar, Prajakta, Ingale, Prajakta, Singh, Shailza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271362/
https://www.ncbi.nlm.nih.gov/pubmed/32548436
http://dx.doi.org/10.1021/acsomega.0c01502
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author Nimsarkar, Prajakta
Ingale, Prajakta
Singh, Shailza
author_facet Nimsarkar, Prajakta
Ingale, Prajakta
Singh, Shailza
author_sort Nimsarkar, Prajakta
collection PubMed
description [Image: see text] Leishmaniasis, the second most neglected tropical disease, has been reported to affect approximately 12 million people worldwide. The causative protozoan parasite Leishmania has shown drug resistance to available chemotherapies, owing to which we need to look for better approaches to deal with the clinical situations. As per recent reports, several miRNAs have been found to be differentially expressed during Leishmania major infection in host macrophages. We aim to evaluate the impact of miRNA-mediated gene regulation on the key players of inflammation and macrophage dysfunction. The origin of Leishmania miRNAs and their processing is a questionable phenomenon as of yet. Through our study, we aim to provide a framework of their characterization. We amalgamate chemical systems biology and synthetic biology approaches to identify putative miRNA targets and unravel the complexity of host–pathogen gene regulatory networks.
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spelling pubmed-72713622020-06-15 Systems Studies Uncover miR-146a as a Target in Leishmania major Infection Model Nimsarkar, Prajakta Ingale, Prajakta Singh, Shailza ACS Omega [Image: see text] Leishmaniasis, the second most neglected tropical disease, has been reported to affect approximately 12 million people worldwide. The causative protozoan parasite Leishmania has shown drug resistance to available chemotherapies, owing to which we need to look for better approaches to deal with the clinical situations. As per recent reports, several miRNAs have been found to be differentially expressed during Leishmania major infection in host macrophages. We aim to evaluate the impact of miRNA-mediated gene regulation on the key players of inflammation and macrophage dysfunction. The origin of Leishmania miRNAs and their processing is a questionable phenomenon as of yet. Through our study, we aim to provide a framework of their characterization. We amalgamate chemical systems biology and synthetic biology approaches to identify putative miRNA targets and unravel the complexity of host–pathogen gene regulatory networks. American Chemical Society 2020-05-18 /pmc/articles/PMC7271362/ /pubmed/32548436 http://dx.doi.org/10.1021/acsomega.0c01502 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Nimsarkar, Prajakta
Ingale, Prajakta
Singh, Shailza
Systems Studies Uncover miR-146a as a Target in Leishmania major Infection Model
title Systems Studies Uncover miR-146a as a Target in Leishmania major Infection Model
title_full Systems Studies Uncover miR-146a as a Target in Leishmania major Infection Model
title_fullStr Systems Studies Uncover miR-146a as a Target in Leishmania major Infection Model
title_full_unstemmed Systems Studies Uncover miR-146a as a Target in Leishmania major Infection Model
title_short Systems Studies Uncover miR-146a as a Target in Leishmania major Infection Model
title_sort systems studies uncover mir-146a as a target in leishmania major infection model
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271362/
https://www.ncbi.nlm.nih.gov/pubmed/32548436
http://dx.doi.org/10.1021/acsomega.0c01502
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