RNA Details
                    Disease Name
                    
                    idiopathic pulmonary fibrosis
                    
                    Tissue
                    
                    uterus
                    
                    RNA Symbol
                    
                    let-7c
                    
                RNA ID
                    
                    
                    
                RNA Type
                    
                    miRNA
                    
                Alteration Pattern
                    
                    dysregulation
                    
                Species
                    
                    homo sapiens
                    
                Detection Methods
                    
                    Dual-luciferase reporter assay; qRT-PCR;  etc.
                    
                Target
                    
                    OLR1
                    
                Pathway
                    
                    NA
                    
                PubMed ID
                    
                    
                    
                    
                    
                Title
                    
                    Exosomal miRNA Let-7 from Menstrual Blood-Derived Endometrial Stem Cells Alleviates Pulmonary Fibrosis through Regulating Mitochondrial DNA Damage
                    
                Year
                    
                     2019
                    
                Function
                    
                    "Mechanistically, Let-7 was able to regulate the expression of lectin-like oxidized low-density lipoprotein receptor-1 (LOX1) through binding to its 3'-UTR region. Forced expression of LOX1 promoted the expression of apoptosis-related protein and mtDNA damage markers via regulating NLRP3 which was also confirmed in BLM model mice under the combination therapy of the exosome and Let-7 inhibitor. Collectively, this study demonstrates that exosomal Let-7 from MenSCs remits pulmonary fibrosis through regulating ROS, mtDNA damage, and NLRP3 inflammasome activation. This provides a new approach of exocytosis on the treatment of fibrotic lung disease."