MicroRNA expression profiles of interstitial lung disease (ILD) patients

ABSTRACT: The mechanisms and molecular pathways underlying interstitial lung diseases (ILDs) are poorly understood. Systems biology approaches were used to identify perturbed networks in these disease states to gain a better understanding of the underlying mechanisms of disease. Through profiling genes and miRNAs, we found subsets of genes and miRNAs that distinguish different disease stages, ILDs from controls, and idiopathic pulmonary fibrosis (IPF) from non-specific interstitial pneumonitis (NSIP). Traditional pathway analysis revealed several disease-associated modules involving genes from the TGF-beta, Wnt, focal adhesion and smooth muscle actin pathways that may be involved in advancing fibrosis. A comprehensively integrative approach was used to construct a global gene regulatory network base

ORGANISM(S): Homo sapiens

SUBMITTER: Ji-Hoon Cho 

PROVIDER: E-GEOD-21394 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress