Key result
Bioinformatics identifies seven key fibrosis biomarkers dysregulated across heart failure and multiple cancer types.
Why the study?
Heart failure and cancer share pathophysiological mechanisms including fibrosis, making the identification of shared biomarkers and therapeutic targets crucial.
Bioinformatics analysis identified seven fibrosis-associated genes (FMOD, POSTN, LTBP2, COL1A1, COL8A1, ASPN, HBB) as potential shared biomarkers and therapeutic targets for both heart failure and various cancers.
These fibrosis genes may link HF and cancer pathways; leaves open biomarker validation and therapeutic targeting in humans.
BACKGROUND: Heart failure (HF) and cancer share common risk factors and pathophysiological mechanisms, including fibrosis. Identifying biomarkers and therapeutic targets for both conditions is crucial. MATERIALS AND METHODS: RNA sequencing data from HF patients were analyzed to identify 12 genes associated with myocardial fibrosis. Validation was performed using public datasets, and functional enrichment analyses were conducted. Gene expression patterns and prognostic value in various cancers were assessed. RESULTS: Fibromodulin (FMOD), Periostin (POSTN), Latent Transforming Growth Factor Beta Binding Protein 2 (LTBP2), Collagen Type I Alpha 1 Chain (COL1A1), Collagen Type VIII Alpha 1 Chain (COL8A1), Asporin (ASPN), and Hemoglobin Subunit Beta (HBB) showed significant dysregulation in heart failure tissues and were implicated in multiple cancer types. Pan-cancer analysis revealed associations between these genes and prognosis. Correlations with cancer-associated fibroblasts were also observed. CONCLUSION: FMOD, POSTN, LTBP2, COL1A1, COL8A1, ASPN, and HBB are potential biomarkers for HF and cancer with fibrotic microenvironments. Targeting fibrosis may offer novel therapeutic approaches. Further validation and mechanistic studies are needed. This study contributes to understanding HF and cancer at the molecular level and suggests personalized treatment strategies.
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Hou et al. (2024) studied Heart failure and cancer (n=99). Bioinformatics analysis of fibrosis-associated genes vs. Normal control samples was evaluated on Identification of differentially expressed genes associated with myocardial fibrosis. Bioinformatics analysis identified FMOD, POSTN, LTBP2, COL1A1, COL8A1, ASPN, and HBB as key fibrosis-associated biomarkers significantly dysregulated in heart failure and multiple cancer types.
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