MicroRNAs (miRNAs) and transcription factors (TFs) play key roles in complex multifactorial diseases like multiple sclerosis (MS). Starting from the miRNomic profile previously associated with a co- hort of pediatric MS (PedMS) patients, we applied a combined mo- lecular and computational approach in order to verify published data in patients with adult-onset MS (AOMS). Six out of the 13 selected miRNAs (miR-320a, miR-125a-5p, miR-652-3p, miR-185-5p, miR- 942-5p, miR-25-3p) were significantly upregulated in PedMS and AOMS patients, suggesting that they may be considered circulating biomarkers distinctive of the disease independently from age. A com- putational and unbiased miRNA-based screening of target genes not necessarily associated to MS was then performed in order to provide an extensive view of the genetic mechanisms underlying the disease. A comprehensive MS-specific miRNA-TF co-regulatory network was hypothesized; among others, SP1, RELA, NF-?B, TP53, AR, MYC, HDAC1, and STAT3 regulated the transcription of 61 targets. Inter- estingly, NF-?B and STAT3 cooperatively regulate the expression of immune response genes and control the cross-talk between inflam- matory and immune cells. Further functional analysis will be per- formed on the identified critical hubs. Above all, in our view, this ap- proach supports the need of multidisciplinary strategies for shedding light into the pathogenesis of MS.
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis
Nicoletta Nuzziello;Laura Vilardo;Paride Pelucchi;Arianna Consiglio;Sabino Liuni;Maria Liguori
2019
Abstract
MicroRNAs (miRNAs) and transcription factors (TFs) play key roles in complex multifactorial diseases like multiple sclerosis (MS). Starting from the miRNomic profile previously associated with a co- hort of pediatric MS (PedMS) patients, we applied a combined mo- lecular and computational approach in order to verify published data in patients with adult-onset MS (AOMS). Six out of the 13 selected miRNAs (miR-320a, miR-125a-5p, miR-652-3p, miR-185-5p, miR- 942-5p, miR-25-3p) were significantly upregulated in PedMS and AOMS patients, suggesting that they may be considered circulating biomarkers distinctive of the disease independently from age. A com- putational and unbiased miRNA-based screening of target genes not necessarily associated to MS was then performed in order to provide an extensive view of the genetic mechanisms underlying the disease. A comprehensive MS-specific miRNA-TF co-regulatory network was hypothesized; among others, SP1, RELA, NF-?B, TP53, AR, MYC, HDAC1, and STAT3 regulated the transcription of 61 targets. Inter- estingly, NF-?B and STAT3 cooperatively regulate the expression of immune response genes and control the cross-talk between inflam- matory and immune cells. Further functional analysis will be per- formed on the identified critical hubs. Above all, in our view, this ap- proach supports the need of multidisciplinary strategies for shedding light into the pathogenesis of MS.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.