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Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives

Gliomas have poor prognosis no matter the treatment applied, remaining an unmet clinical need. As background for a substantial change in this situation, this review will focus on the following points: (i) the steady progress in establishing the role of molecular chaperones in carcinogenesis; (ii) th...

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Autores principales: Caruso Bavisotto, Celeste, Graziano, Francesca, Rappa, Francesca, Marino Gammazza, Antonella, Logozzi, Mariantonia, Fais, Stefano, Maugeri, Rosario, Bucchieri, Fabio, Conway de Macario, Everly, Macario, Alberto J. L., Cappello, Francesco, Iacopino, Domenico G., Campanella, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164348/
https://www.ncbi.nlm.nih.gov/pubmed/30189598
http://dx.doi.org/10.3390/ijms19092626
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author Caruso Bavisotto, Celeste
Graziano, Francesca
Rappa, Francesca
Marino Gammazza, Antonella
Logozzi, Mariantonia
Fais, Stefano
Maugeri, Rosario
Bucchieri, Fabio
Conway de Macario, Everly
Macario, Alberto J. L.
Cappello, Francesco
Iacopino, Domenico G.
Campanella, Claudia
author_facet Caruso Bavisotto, Celeste
Graziano, Francesca
Rappa, Francesca
Marino Gammazza, Antonella
Logozzi, Mariantonia
Fais, Stefano
Maugeri, Rosario
Bucchieri, Fabio
Conway de Macario, Everly
Macario, Alberto J. L.
Cappello, Francesco
Iacopino, Domenico G.
Campanella, Claudia
author_sort Caruso Bavisotto, Celeste
collection PubMed
description Gliomas have poor prognosis no matter the treatment applied, remaining an unmet clinical need. As background for a substantial change in this situation, this review will focus on the following points: (i) the steady progress in establishing the role of molecular chaperones in carcinogenesis; (ii) the recent advances in the knowledge of miRNAs in regulating gene expression, including genes involved in carcinogenesis and genes encoding chaperones; and (iii) the findings about exosomes and their cargo released by tumor cells. We would like to trigger a discussion about the involvement of exosomal chaperones and miRNAs in gliomagenesis. Chaperones may be either targets for therapy, due to their tumor-promoting activity, or therapeutic agents, due to their antitumor growth activity. Thus, chaperones may well represent a Janus-faced approach against tumors. This review focuses on extracellular chaperones as part of exosomes’ cargo, because of their potential as a new tool for the diagnosis and management of gliomas. Moreover, since exosomes transport chaperones and miRNAs (the latter possibly related to chaperone gene expression in the recipient cell), and probably deliver their cargo in the recipient cells, a new area of investigation is now open, which is bound to generate significant advances in the understanding and treatment of gliomas.
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spelling pubmed-61643482018-10-10 Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives Caruso Bavisotto, Celeste Graziano, Francesca Rappa, Francesca Marino Gammazza, Antonella Logozzi, Mariantonia Fais, Stefano Maugeri, Rosario Bucchieri, Fabio Conway de Macario, Everly Macario, Alberto J. L. Cappello, Francesco Iacopino, Domenico G. Campanella, Claudia Int J Mol Sci Review Gliomas have poor prognosis no matter the treatment applied, remaining an unmet clinical need. As background for a substantial change in this situation, this review will focus on the following points: (i) the steady progress in establishing the role of molecular chaperones in carcinogenesis; (ii) the recent advances in the knowledge of miRNAs in regulating gene expression, including genes involved in carcinogenesis and genes encoding chaperones; and (iii) the findings about exosomes and their cargo released by tumor cells. We would like to trigger a discussion about the involvement of exosomal chaperones and miRNAs in gliomagenesis. Chaperones may be either targets for therapy, due to their tumor-promoting activity, or therapeutic agents, due to their antitumor growth activity. Thus, chaperones may well represent a Janus-faced approach against tumors. This review focuses on extracellular chaperones as part of exosomes’ cargo, because of their potential as a new tool for the diagnosis and management of gliomas. Moreover, since exosomes transport chaperones and miRNAs (the latter possibly related to chaperone gene expression in the recipient cell), and probably deliver their cargo in the recipient cells, a new area of investigation is now open, which is bound to generate significant advances in the understanding and treatment of gliomas. MDPI 2018-09-05 /pmc/articles/PMC6164348/ /pubmed/30189598 http://dx.doi.org/10.3390/ijms19092626 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Caruso Bavisotto, Celeste
Graziano, Francesca
Rappa, Francesca
Marino Gammazza, Antonella
Logozzi, Mariantonia
Fais, Stefano
Maugeri, Rosario
Bucchieri, Fabio
Conway de Macario, Everly
Macario, Alberto J. L.
Cappello, Francesco
Iacopino, Domenico G.
Campanella, Claudia
Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives
title Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives
title_full Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives
title_fullStr Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives
title_full_unstemmed Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives
title_short Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives
title_sort exosomal chaperones and mirnas in gliomagenesis: state-of-art and theranostics perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164348/
https://www.ncbi.nlm.nih.gov/pubmed/30189598
http://dx.doi.org/10.3390/ijms19092626
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