RNA Details
                    Disease Name
                    
                    idiopathic pulmonary fibrosis
                    
                    Tissue
                    
                    lung
                    
                    RNA Symbol
                    
                    mir-26a-1
                    
                RNA ID
                    
                    
                    
                RNA Type
                    
                    miRNA
                    
                Alteration Pattern
                    
                    dysregulation
                    
                Species
                    
                    homo sapiens
                    
                Detection Methods
                    
                    qRT-PCR; Masson's trichrome staining;  etc.
                    
                Target
                    
                    CTGF; SMAD4
                    
                Pathway
                    
                    NA
                    
                PubMed ID
                    
                    
                    
                    
                    
                Title
                    
                    The antifibrotic effects and mechanisms of microRNA-26a action in idiopathic pulmonary fibrosis
                    
                Year
                    
                     2014
                    
                Function
                    
                    "Downregulation of miR-26a in the lungs of mice with experimental pulmonary fibrosis and in IPF resulted in posttranscriptional derepression of connective tissue growth factor (CTGF), and induced collagen production. Inhibition of miR-26a in the lungs caused pulmonary fibrosis in vivo, whereas overexpression of miR-26a repressed transforming growth factor (TGF)-B1-induced fibrogenesis in MRC-5 cells and attenuated experimental pulmonary fibrosis in mice. MiR-26a was downregulated by TGF-B1-mediated phosphorylation of Smad3. Moreover, miR-26a inhibited the nuclear translocation of p-Smad3 through directly targeting Smad4, which determines the nuclear translocation of p-Smad2/Smad3."