RNA Details
                    Disease Name
                    
                    idiopathic pulmonary fibrosis
                    
                    Tissue
                    
                    lung
                    
                    RNA Symbol
                    
                    mir-29a
                    
                RNA ID
                    
                    
                    
                RNA Type
                    
                    miRNA
                    
                Alteration Pattern
                    
                    down regulation
                    
                Species
                    
                    homo sapiens
                    
                Detection Methods
                    
                    qRT-PCR;  Dual-luciferase reporter assay etc.
                    
                Target
                    
                    LOXL2; SERPINH1
                    
                Pathway
                    
                    NA
                    
                PubMed ID
                    
                    
                    
                    
                    
                Title
                    
                    Regulation of LOXL2 and SERPINH1 by antitumor microRNA-29a in lung cancer with idiopathic pulmonary fibrosis
                    
                Year
                    
                     2016
                    
                Function
                    
                    "MiR-29a is downregulated in clinical specimens of IPF and lung cancer. Restoration of miR-29a suppressed cancer cell aggressiveness and fibroblast migration.Lysyl oxidase-like 2 (LOXL2) and serpin peptidase inhibitor clade H, member 1 (SERPINH1) were direct targets of miR-29a, contributing significantly to collagen biosynthesis. Overexpression of LOXL2 and SERPINH1 was observed in clinical specimens of lung cancer and fibrotic lesions. Downregulation of miR-29a caused overexpression of LOXL2 and SERPINH1 in lung cancer and IPF, suggesting that these genes are involved in the pathogenesis of these two diseases."