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Cell death pathways and viruses: Role of microRNAs

Viral infections lead to the death of more than a million people each year around the world, both directly and indirectly. Viruses interfere with many cell functions, particularly critical pathways for cell death, by affecting various intracellular mediators. MicroRNAs (miRNAs) are a major example o...

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Autores principales: Sadri Nahand, Javid, Shojaie, Layla, Akhlagh, Seyed Amirreza, Ebrahimi, Mohammad Saeid, Mirzaei, Hamid Reza, Bannazadeh Baghi, Hossein, Mahjoubin-Tehran, Maryam, Rezaei, Nima, Hamblin, Michael R., Tajiknia, Vida, Rahimian, Neda, Mirzaei, Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056183/
https://www.ncbi.nlm.nih.gov/pubmed/33898103
http://dx.doi.org/10.1016/j.omtn.2021.03.011
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author Sadri Nahand, Javid
Shojaie, Layla
Akhlagh, Seyed Amirreza
Ebrahimi, Mohammad Saeid
Mirzaei, Hamid Reza
Bannazadeh Baghi, Hossein
Mahjoubin-Tehran, Maryam
Rezaei, Nima
Hamblin, Michael R.
Tajiknia, Vida
Rahimian, Neda
Mirzaei, Hamed
author_facet Sadri Nahand, Javid
Shojaie, Layla
Akhlagh, Seyed Amirreza
Ebrahimi, Mohammad Saeid
Mirzaei, Hamid Reza
Bannazadeh Baghi, Hossein
Mahjoubin-Tehran, Maryam
Rezaei, Nima
Hamblin, Michael R.
Tajiknia, Vida
Rahimian, Neda
Mirzaei, Hamed
author_sort Sadri Nahand, Javid
collection PubMed
description Viral infections lead to the death of more than a million people each year around the world, both directly and indirectly. Viruses interfere with many cell functions, particularly critical pathways for cell death, by affecting various intracellular mediators. MicroRNAs (miRNAs) are a major example of these mediators because they are involved in many (if not most) cellular mechanisms. Virus-regulated miRNAs have been implicated in three cell death pathways, namely, apoptosis, autophagy, and anoikis. Several molecules (e.g., BECN1 and B cell lymphoma 2 [BCL2] family members) are involved in both apoptosis and autophagy, while activation of anoikis leads to cell death similar to apoptosis. These mechanistic similarities suggest that common regulators, including some miRNAs (e.g., miR-21 and miR-192), are involved in different cell death pathways. Because the balance between cell proliferation and cell death is pivotal to the homeostasis of the human body, miRNAs that regulate cell death pathways have drawn much attention from researchers. miR-21 is regulated by several viruses and can affect both apoptosis and anoikis via modulating various targets, such as PDCD4, PTEN, interleukin (IL)-12, Maspin, and Fas-L. miR-34 can be downregulated by viral infection and has different effects on apoptosis, depending on the type of virus and/or host cell. The present review summarizes the existing knowledge on virus-regulated miRNAs involved in the modulation of cell death pathways. Understanding the mechanisms for virus-mediated regulation of cell death pathways could provide valuable information to improve the diagnosis and treatment of many viral diseases.
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spelling pubmed-80561832021-04-23 Cell death pathways and viruses: Role of microRNAs Sadri Nahand, Javid Shojaie, Layla Akhlagh, Seyed Amirreza Ebrahimi, Mohammad Saeid Mirzaei, Hamid Reza Bannazadeh Baghi, Hossein Mahjoubin-Tehran, Maryam Rezaei, Nima Hamblin, Michael R. Tajiknia, Vida Rahimian, Neda Mirzaei, Hamed Mol Ther Nucleic Acids Review Viral infections lead to the death of more than a million people each year around the world, both directly and indirectly. Viruses interfere with many cell functions, particularly critical pathways for cell death, by affecting various intracellular mediators. MicroRNAs (miRNAs) are a major example of these mediators because they are involved in many (if not most) cellular mechanisms. Virus-regulated miRNAs have been implicated in three cell death pathways, namely, apoptosis, autophagy, and anoikis. Several molecules (e.g., BECN1 and B cell lymphoma 2 [BCL2] family members) are involved in both apoptosis and autophagy, while activation of anoikis leads to cell death similar to apoptosis. These mechanistic similarities suggest that common regulators, including some miRNAs (e.g., miR-21 and miR-192), are involved in different cell death pathways. Because the balance between cell proliferation and cell death is pivotal to the homeostasis of the human body, miRNAs that regulate cell death pathways have drawn much attention from researchers. miR-21 is regulated by several viruses and can affect both apoptosis and anoikis via modulating various targets, such as PDCD4, PTEN, interleukin (IL)-12, Maspin, and Fas-L. miR-34 can be downregulated by viral infection and has different effects on apoptosis, depending on the type of virus and/or host cell. The present review summarizes the existing knowledge on virus-regulated miRNAs involved in the modulation of cell death pathways. Understanding the mechanisms for virus-mediated regulation of cell death pathways could provide valuable information to improve the diagnosis and treatment of many viral diseases. American Society of Gene & Cell Therapy 2021-03-19 /pmc/articles/PMC8056183/ /pubmed/33898103 http://dx.doi.org/10.1016/j.omtn.2021.03.011 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sadri Nahand, Javid
Shojaie, Layla
Akhlagh, Seyed Amirreza
Ebrahimi, Mohammad Saeid
Mirzaei, Hamid Reza
Bannazadeh Baghi, Hossein
Mahjoubin-Tehran, Maryam
Rezaei, Nima
Hamblin, Michael R.
Tajiknia, Vida
Rahimian, Neda
Mirzaei, Hamed
Cell death pathways and viruses: Role of microRNAs
title Cell death pathways and viruses: Role of microRNAs
title_full Cell death pathways and viruses: Role of microRNAs
title_fullStr Cell death pathways and viruses: Role of microRNAs
title_full_unstemmed Cell death pathways and viruses: Role of microRNAs
title_short Cell death pathways and viruses: Role of microRNAs
title_sort cell death pathways and viruses: role of micrornas
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056183/
https://www.ncbi.nlm.nih.gov/pubmed/33898103
http://dx.doi.org/10.1016/j.omtn.2021.03.011
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