| Literature DB >> 33562569 |
Georgia Mandolesi1,2, Francesca Romana Rizzo3, Sara Balletta3, Mario Stampanoni Bassi4, Luana Gilio4, Livia Guadalupi1,3, Monica Nencini1, Alessandro Moscatelli3,5, Colleen Patricia Ryan3,5, Valerio Licursi6, Ettore Dolcetti3, Alessandra Musella1,2, Antonietta Gentile1, Diego Fresegna1, Silvia Bullitta1,3, Silvia Caioli4, Valentina Vanni1,3, Krizia Sanna3, Antonio Bruno3, Fabio Buttari4, Chiara Castelli6, Carlo Presutti6, Francesca De Santa7, Annamaria Finardi8, Roberto Furlan8, Diego Centonze3,4, Francesca De Vito4.
Abstract
The identification of microRNAs in biological fluids for diagnosis and prognosis is receiving great attention in the field of multiple sclerosis (MS) research but it is still in its infancy. In the present study, we observed in a large sample of MS patients that let-7b-5p levels in the cerebrospinal fluid (CSF) were highly correlated with a number of microRNAs implicated in MS, as well as with a variety of inflammation-related protein factors, showing specific expression patterns coherent with let-7b-5p-mediated regulation. Additionally, we found that the CSF let-7b-5p levels were significantly reduced in patients with the progressive MS compared to patients with relapsing-remitting MS and were negatively correlated with characteristic hallmark processes of the two phases of the disease. Indeed, in the non-progressive phase, let-7b-5p inversely associated with both central and peripheral inflammation; whereas, in progressive MS, the CSF levels of let-7b-5p negatively correlated with clinical disability at disease onset and after a follow-up period. Overall, our results uncovered, by the means of a multidisciplinary approach and multiple statistical analyses, a new possible pleiotropic action of let-7b-5p in MS, with potential utility as a biomarker of MS course.Entities:
Keywords: Expanded Disability Status Scale (EDSS); G_CSF; IL5; RANTES; inflammation; let-7; miRNAs; multiple sclerosis (MS); progressive multiple sclerosis (PMS)
Year: 2021 PMID: 33562569 PMCID: PMC7915741 DOI: 10.3390/cells10020330
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600