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  5. MicroRNA let-7 and viral infections: focus on mechanisms of action

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Article
en
2022

MicroRNA let-7 and viral infections: focus on mechanisms of action

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0 Files

en
2022
Vol 27 (1)
Vol. 27
DOI: 10.1186/s11658-022-00317-9

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Michael R Hamblin
Michael R Hamblin

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Arash Letafati
Sajad Najafi
Mehran Mottahedi
+10 more

Abstract

MicroRNAs (miRNAs) are fundamental post-transcriptional modulators of several critical cellular processes, a number of which are involved in host defense mechanisms. In particular, miRNA let-7 functions as an essential regulator of the function and differentiation of both innate and adaptive immune cells. Let-7 is involved in several human diseases, including cancer and viral infections. Several viral infections have found ways to dysregulate the expression of miRNAs. Extracellular vesicles (EV) are membrane-bound lipid structures released from many types of human cells that can transport proteins, lipids, mRNAs, and miRNAs, including let-7. After their release, EVs are taken up by the recipient cells and their contents released into the cytoplasm. Let-7-loaded EVs have been suggested to affect cellular pathways and biological targets in the recipient cells, and can modulate viral replication, the host antiviral response, and the action of cancer-related viruses. In the present review, we summarize the available knowledge concerning the expression of let-7 family members, functions, target genes, and mechanistic involvement in viral pathogenesis and host defense. This may provide insight into the development of new therapeutic strategies to manage viral infections.

How to cite this publication

Arash Letafati, Sajad Najafi, Mehran Mottahedi, Mohammad Reza Karimzadeh, Ali Shahini, Setareh Garousi, Mohammad Abbasi‐Kolli, Javid Sadri Nahand, Seyed Saeed Tamehri Zadeh, Michael R Hamblin, Neda Rahimian, Mohammad Taghizadieh, Hamed Mirzaei (2022). MicroRNA let-7 and viral infections: focus on mechanisms of action. , 27(1), DOI: https://doi.org/10.1186/s11658-022-00317-9.

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Publication Details

Type

Article

Year

2022

Authors

13

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1186/s11658-022-00317-9

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