TY - JOUR
T1 - Exosomal Chaperones and miRNAs in Gliomagenesis: State-of-Art and Theranostics Perspectives
AU - Graziano, Francesca
AU - Cappello, Francesco
AU - Marino Gammazza, Antonella
AU - Campanella, Claudia
AU - Bucchieri, Fabio
AU - Rappa, Francesca
AU - Caruso Bavisotto, Celeste
AU - Iacopino, Domenico
AU - Campanella, Claudia
AU - Gammazza, Antonella Marino
AU - Rappa, Francesca
AU - Bavisotto, Celeste Caruso
AU - Logozzi, Mariantonia
AU - De Macario, Everly Conway
AU - Fais, Stefano
AU - Cappello, Francesco
AU - De Macario, Everly Conway
AU - Macario, Alberto J. L.
PY - 2018
Y1 - 2018
N2 - 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.
AB - 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.
KW - Hsp60
KW - Hsps (Heat shock proteins)
KW - exosomes
KW - extracellular vesicles
KW - gliomas
KW - miRNA
KW - molecular chaperones
KW - theranostic tools
KW - Hsp60
KW - Hsps (Heat shock proteins)
KW - exosomes
KW - extracellular vesicles
KW - gliomas
KW - miRNA
KW - molecular chaperones
KW - theranostic tools
UR - http://hdl.handle.net/10447/296928
M3 - Article
SN - 1661-6596
SP - 1
EP - 20
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
ER -