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Título
miRNAs in the regulation of mTOR signaling and host immune responses: The case of Leishmania infections
Autor(es)
Palabras clave
ARN
Leishmaniasis
Parásitos
Clasificación UNESCO
3207.12 Parasitología
2412 Inmunología
Fecha de publicación
2022
Editor
Elsevier
Citación
Rashidi, S., Mansouri, R., Ali-Hassanzadeh, M., Ghani, E., Karimazar, M., Muro, A., ... & Manzano-Román, R. (2022). miRNAs in the regulation of mTOR signaling and host immune responses: the case of Leishmania infections. Acta Tropica, 231, 106431.
Resumen
[EN] Micro RNAs (miRNAs), as regulators of gene expression at the post-transcriptional level, can respond to/or
interact with cell signaling and affect the pathogenesis of different diseases/infections. The interaction/crosstalk
of miRNAs with various cellular signaling networks including mTOR (as a master regulator of signaling relevant
to different cellular mechanisms) might lead to the initiation, progression or restriction of certain disease processes.
There are numerous studies that have identified the crosstalk between regulatory miRNA expression and
the mTOR pathway (or mTOR signaling regulated by miRNAs) in different diseases which has a dual function in
pathogenesis. However, the corresponding information in parasitic infections remains scarce. miRNAs have been
suggested as specific targets for therapeutic strategies in several disorders such as parasitic infections. Thus, the
targeting of miRNAs (as the modulators/regulators of mTOR) by small molecules and RNA-based therapeutics
and consequently managing and modulating mTOR signaling and the downstream/related cell signaling/pathways
might shed some light on the design of new therapeutic strategies against parasitic diseases, including
Leishmaniasis. Accordingly, the present study attempts to highlight the importance of the crosstalk between
regulatory miRNAs and mTOR signaling, and to review the relevant insights into parasitic infections by focusing
specifically on Leishmania.
URI
ISSN
0001-706X
DOI
10.1016/j.actatropica.2022.106431
Versión del editor
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Patrocinador
Publicación en abierto financiada por la Universidad de Salamanca como participante en el Acuerdo Transformativo CRUE-CSIC con Elsevier, 2021-2024













