Dusting Off IL-9 as a New Therapeutic Target for Pulmonary Fibrosis.
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ABSTRACT:
SUBMITTER: Rojas-Quintero J
PROVIDER: S-EPMC6376410 | biostudies-literature | 2019 Feb
REPOSITORIES: biostudies-literature
Publications
Dusting Off IL-9 as a New Therapeutic Target for Pulmonary Fibrosis.
Rojas-Quintero Joselyn J Wang Xiaoyun X Owen Caroline A CA
American journal of respiratory cell and molecular biology 20190201 2
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Project description:IL-11 is a therapeutic target in idiopathic pulmonary fibrosis
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Project description:BackgroundGlycolysis plays a major role in progression of idiopathic pulmonary fibrosis (IPF). Here, we aim to explore the predictive signature based on glycolysis-related genes for predicting the prognosis and identified a potential therapeutic target for IPF.MethodsGene expression data of bronchoalveolar lavage (BAL) cells and clinical information were downloaded from the Gene Expression Omnibus database. Bioinformatic analysis was then performed to identify differentially expressed genes (DEGs). Lasso multivariate cox analysis and multivariate Cox regression were used to establish a gene signature. The prediction model was evaluated using the time-dependent receiver operating characteristic (ROC) curve and validated using an external independent dataset. The expression of these key genes in cellular level analyzed from Single Cell Expression Atlas. Cell Counting Kit-8 assay, immunofluorescence, wound healing and plasmid transfection were performed.ResultsA total of 4 gene (ANGPTL4, ME2, TPBG and IER3), which were associated with the prognosis of IPF patients, were selected to establish our signature. The prediction model was an independent prognostic indicator for IPF patients. ANGPTL4 was significantly upregulated in pleural mesothelial cells (PMCs). In vitro assay showed that ANGPTL4 promoted PMCs proliferation and migration. Knockdown of ANGPTL4 can inhibit mesothelial-mesenchymal transition by suppressed glycolysis-associated gene, such as PGM1, GPI, PGK1, LDHA, ALDOA, ENO1 and TPI1.ConclusionsOur research established a glycolysis-associated gene signature that holds potential to assist clinicians in the personalized management of IPF. Furthermore, we identified that ANGPTL4 mediates mesothelial-mesenchymal transition, suggesting its viability as a therapeutic target for IPF treatment.
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