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pmid:31093274
Expression Analysis of Fibronectin Type III Domain-Containing (FNDC) Genes in Inflammatory Bowel Disease and Colorectal Cancer.
Tilo Wuensch · Jonas Wizenty · Janina Quint · Wolfgang Spitz · Madeleen Bosma · Olaf Becker · Andreas Adler · Wilfried Veltzke-Schlieker · Martin Stockmann · Sascha Weiss · Matthias Biebl · Johann Pratschke · Felix Aigner
Gastroenterology research and practice · 2019 doi:10.1155/2019/3784172
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Experiment
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Data
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Analysis
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Complete file
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FNDC4 was described as anti-inflammatory factor, upregulated in inflammatory bowel disease (IBD). FNDC signaling includes direct cell-cell interaction as well as release of bioactive peptides, like shown for FNDC4 or FNDC5. The G-protein-coupled receptor 116 (GPR116) was found as a putative FNDC4 receptor. We here aim to comprehensively analyze the mRNA expression of FNDC1, FNDC3A, FNDC3B, FNDC4, FNDC5, and GPR116 in nonaffected and affected mucosal samples of patients with IBD or colorectal cancer (CRC).\nMETHODS: Mucosa samples were obtained from 30 patients undergoing diagnostic colonoscopy or from surgical resection of IBD or CRC. Gene expression was determined by quantitative real-time PCR. In addition, FNDC expression data from publicly available Gene Expression Omnibus (GEO) data sets (GDS4296, GDS4515, and GDS5232) were analyzed.\nRESULTS: Basal mucosal expression revealed higher expression of FNDC3A and FNDC5 in the ileum compared to colonic segments. FNDC1 and FNDC4 were significantly upregulated in IBD. None of the investigated FNDCs was differentially expressed in CRC, just FNDC3A trended to be upregulated. The GEO data set analysis revealed significantly downregulated FNDC4 and upregulated GPR116 in microsatellite unstable (MSI) CRCs. The expression of FNDCs and GPR116 was independent of age and sex.\nCONCLUSIONS: FNDC1 and FNDC4 may play a relevant role in the pathobiology of IBD, but none of the investigated FNDCs is regulated in CRC. GPR116 may be upregulated in advanced or MSI CRC. Further studies should validate the altered FNDC expression results on protein levels and examine the corresponding functional consequences.", "claims": [{"id": "claim-method", "statement": "Data sets containing array-based gene expression profile data (normalized expression values) were retrieved from the Gene Expression Omnibus (GEO) platform. 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The normalized expression values (given in arbitrary units) were analyzed for differential gene expression of FNDCs and GPR116 in CRC cell lines (GDS4296) and microsatellite unstable carcinoma (MSI CRCs) (GDS4515) as well as in early- vs. late-onset carcinoma in males and female (GDS5232), using one-way ANOVA for multiple comparison test and t-tests for comparing two groups."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data used to support the findings of this study are available from the corresponding author upon request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:31093274", "locator": "sections[17] \"Data Availability\" paragraph 2", "quote": "All data used to support the findings of this study are available from the corresponding author upon request."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:31093274"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "blocked", "blocked_on": "data:accession_absent", "description": "The GEO series accession resolves and its sample accessions are listed. 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