Cargando…

Non-coding RNA in idiopathic interstitial pneumonia and Covid-19 pulmonary fibrosis

Pulmonary fibrosis is the key feature of majority of idiopathic interstitial pneumonias (IIPs) as well as many patients with post-COVID-19. The pathogenesis of pulmonary fibrosis is a complex molecular process that involves myriad of cells, proteins, genes, and regulatory elements. The non-coding RN...

Descripción completa

Detalles Bibliográficos
Autores principales: Ali, Mohammad Shadab, Singh, Jay, Alam, Md Tanjim, Chopra, Anita, Arava, Sudheer, Bhalla, Ashu Seith, Mittal, Saurabh, Mohan, Anant, Mitra, Dipendra K, Hadda, Vijay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467421/
https://www.ncbi.nlm.nih.gov/pubmed/36097114
http://dx.doi.org/10.1007/s11033-022-07820-4
_version_ 1784788191691145216
author Ali, Mohammad Shadab
Singh, Jay
Alam, Md Tanjim
Chopra, Anita
Arava, Sudheer
Bhalla, Ashu Seith
Mittal, Saurabh
Mohan, Anant
Mitra, Dipendra K
Hadda, Vijay
author_facet Ali, Mohammad Shadab
Singh, Jay
Alam, Md Tanjim
Chopra, Anita
Arava, Sudheer
Bhalla, Ashu Seith
Mittal, Saurabh
Mohan, Anant
Mitra, Dipendra K
Hadda, Vijay
author_sort Ali, Mohammad Shadab
collection PubMed
description Pulmonary fibrosis is the key feature of majority of idiopathic interstitial pneumonias (IIPs) as well as many patients with post-COVID-19. The pathogenesis of pulmonary fibrosis is a complex molecular process that involves myriad of cells, proteins, genes, and regulatory elements. The non-coding RNA mainly miRNA, circRNA, and lncRNA are among the key regulators of many protein coding genes and pathways that are involved in pulmonary fibrosis. Identification and molecular mechanisms, by which these non-coding RNA molecules work, are crucial to understand the molecular basis of the disease. Additionally, elucidation of molecular mechanism could also help in deciphering a potential diagnostic/prognostic marker as well as therapeutic targets for IIPs and post-COVID-19 pulmonary fibrosis. In this review, we have provided the latest findings and discussed the role of these regulatory elements in the pathogenesis of pulmonary fibrosis associated with Idiopathic Interstitial Pneumonia and Covid-19.
format Online
Article
Text
id pubmed-9467421
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer Netherlands
record_format MEDLINE/PubMed
spelling pubmed-94674212022-09-13 Non-coding RNA in idiopathic interstitial pneumonia and Covid-19 pulmonary fibrosis Ali, Mohammad Shadab Singh, Jay Alam, Md Tanjim Chopra, Anita Arava, Sudheer Bhalla, Ashu Seith Mittal, Saurabh Mohan, Anant Mitra, Dipendra K Hadda, Vijay Mol Biol Rep Original Article Pulmonary fibrosis is the key feature of majority of idiopathic interstitial pneumonias (IIPs) as well as many patients with post-COVID-19. The pathogenesis of pulmonary fibrosis is a complex molecular process that involves myriad of cells, proteins, genes, and regulatory elements. The non-coding RNA mainly miRNA, circRNA, and lncRNA are among the key regulators of many protein coding genes and pathways that are involved in pulmonary fibrosis. Identification and molecular mechanisms, by which these non-coding RNA molecules work, are crucial to understand the molecular basis of the disease. Additionally, elucidation of molecular mechanism could also help in deciphering a potential diagnostic/prognostic marker as well as therapeutic targets for IIPs and post-COVID-19 pulmonary fibrosis. In this review, we have provided the latest findings and discussed the role of these regulatory elements in the pathogenesis of pulmonary fibrosis associated with Idiopathic Interstitial Pneumonia and Covid-19. Springer Netherlands 2022-09-12 2022 /pmc/articles/PMC9467421/ /pubmed/36097114 http://dx.doi.org/10.1007/s11033-022-07820-4 Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Ali, Mohammad Shadab
Singh, Jay
Alam, Md Tanjim
Chopra, Anita
Arava, Sudheer
Bhalla, Ashu Seith
Mittal, Saurabh
Mohan, Anant
Mitra, Dipendra K
Hadda, Vijay
Non-coding RNA in idiopathic interstitial pneumonia and Covid-19 pulmonary fibrosis
title Non-coding RNA in idiopathic interstitial pneumonia and Covid-19 pulmonary fibrosis
title_full Non-coding RNA in idiopathic interstitial pneumonia and Covid-19 pulmonary fibrosis
title_fullStr Non-coding RNA in idiopathic interstitial pneumonia and Covid-19 pulmonary fibrosis
title_full_unstemmed Non-coding RNA in idiopathic interstitial pneumonia and Covid-19 pulmonary fibrosis
title_short Non-coding RNA in idiopathic interstitial pneumonia and Covid-19 pulmonary fibrosis
title_sort non-coding rna in idiopathic interstitial pneumonia and covid-19 pulmonary fibrosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467421/
https://www.ncbi.nlm.nih.gov/pubmed/36097114
http://dx.doi.org/10.1007/s11033-022-07820-4
work_keys_str_mv AT alimohammadshadab noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT singhjay noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT alammdtanjim noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT chopraanita noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT aravasudheer noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT bhallaashuseith noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT mittalsaurabh noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT mohananant noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT mitradipendrak noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis
AT haddavijay noncodingrnainidiopathicinterstitialpneumoniaandcovid19pulmonaryfibrosis