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Circulating miRNAs as new activators of the JAK-STAT3 pathway

Cell communication is well known to rely on direct contacts or on secreted factors that bind to receptors located on the surface of their target cells. In addition to this classical pathway, recent results have shown that cells produce microvesicles that contain functional DNA, RNA and proteins that...

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Detalles Bibliográficos
Autores principales: Lam, David, Barré, Benjamin, Guette, Catherine, Coqueret, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670266/
https://www.ncbi.nlm.nih.gov/pubmed/24058790
http://dx.doi.org/10.4161/jkst.22996
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author Lam, David
Barré, Benjamin
Guette, Catherine
Coqueret, Olivier
author_facet Lam, David
Barré, Benjamin
Guette, Catherine
Coqueret, Olivier
author_sort Lam, David
collection PubMed
description Cell communication is well known to rely on direct contacts or on secreted factors that bind to receptors located on the surface of their target cells. In addition to this classical pathway, recent results have shown that cells produce microvesicles that contain functional DNA, RNA and proteins that can be directly transferred to recipient cells. This induces proliferation, differentiation or cell death to the same extent as classical soluble factors. New data obtained from the laboratory of Napoleone Ferrara show that these microvesicles also contain miRNAs that can induce angiogenic activities in neighboring endothelial cells. When secreted from cancer cells, these miRNA-loaded vesicles penetrate recipient cells where they activate the JAK-STAT pathway. This represents a new type of intercellular signaling and a new way of activating the STAT transcription factors that could be of interest for the design of cancer treatments.
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spelling pubmed-36702662013-09-19 Circulating miRNAs as new activators of the JAK-STAT3 pathway Lam, David Barré, Benjamin Guette, Catherine Coqueret, Olivier JAKSTAT Commentary Cell communication is well known to rely on direct contacts or on secreted factors that bind to receptors located on the surface of their target cells. In addition to this classical pathway, recent results have shown that cells produce microvesicles that contain functional DNA, RNA and proteins that can be directly transferred to recipient cells. This induces proliferation, differentiation or cell death to the same extent as classical soluble factors. New data obtained from the laboratory of Napoleone Ferrara show that these microvesicles also contain miRNAs that can induce angiogenic activities in neighboring endothelial cells. When secreted from cancer cells, these miRNA-loaded vesicles penetrate recipient cells where they activate the JAK-STAT pathway. This represents a new type of intercellular signaling and a new way of activating the STAT transcription factors that could be of interest for the design of cancer treatments. Landes Bioscience 2013-01-01 2013-01-01 /pmc/articles/PMC3670266/ /pubmed/24058790 http://dx.doi.org/10.4161/jkst.22996 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Commentary
Lam, David
Barré, Benjamin
Guette, Catherine
Coqueret, Olivier
Circulating miRNAs as new activators of the JAK-STAT3 pathway
title Circulating miRNAs as new activators of the JAK-STAT3 pathway
title_full Circulating miRNAs as new activators of the JAK-STAT3 pathway
title_fullStr Circulating miRNAs as new activators of the JAK-STAT3 pathway
title_full_unstemmed Circulating miRNAs as new activators of the JAK-STAT3 pathway
title_short Circulating miRNAs as new activators of the JAK-STAT3 pathway
title_sort circulating mirnas as new activators of the jak-stat3 pathway
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670266/
https://www.ncbi.nlm.nih.gov/pubmed/24058790
http://dx.doi.org/10.4161/jkst.22996
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