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New DNA methylation signals for malignant pleural mesothelioma risk assessment

Title: New DNA methylation signals for malignant pleural mesothelioma risk assessment
Authors: Cugliari G.; Allione A.; Russo A.; Catalano C.; Casalone E.; Guarrera S.; Grosso F.; Ferrante D.; Sculco M.; La Vecchia M.; Pirazzini C.; Libener R.; Mirabelli D.; Magnani C.; Dianzani I.; Matullo G.
Contributors: Cugliari G.; Allione A.; Russo A.; Catalano C.; Casalone E.; Guarrera S.; Grosso F.; Ferrante D.; Sculco M.; La Vecchia M.; Pirazzini C.; Libener R.; Mirabelli D.; Magnani C.; Dianzani I.; Matullo G.
Publication Year: 2021
Collection: Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto)
Subject Terms: Asbestos exposure; DNA methylation; Epigenome-wide analysi; Interaction analysi; Malignant pleural mesothelioma
Description: Malignant pleural mesothelioma (MPM) is a rare and aggressive neoplasm. Patients are usually diagnosed when current treatments have limited benefits, highlighting the need for noninva-sive tests aimed at an MPM risk assessment tool that might improve life expectancy. Three hundred asbestos-exposed subjects (163 MPM cases and 137 cancer-free controls), from the same geographical region in Italy, were recruited. The evaluation of asbestos exposure was conducted considering the frequency, the duration and the intensity of occupational, environmental and domestic exposure. A genome-wide methylation array was performed to identify novel blood DNA methylation (DNAm) markers of MPM. Multiple regression analyses adjusting for potential confounding factors and interaction between asbestos exposure and DNAm on the MPM odds ratio were applied. Epigenome-wide analysis (EWAS) revealed 12 single-CpGs associated with the disease. Two of these showed high statistical power (99%) and effect size (>0.05) after false discovery rate (FDR) multiple comparison corrections: (i) cg03546163 in FKBP5, significantly hypomethylated in cases (Mean Difference in beta values (MD) = −0.09, 95% CI = −0.12|−0.06, p = 1.2 × 10−7), and (ii) cg06633438 in MLLT1, statistically hypermethylated in cases (MD = 0.07, 95% CI = 0.04|0.10, p = 1.0 × 10−6). Based on the interaction analysis, asbestos exposure and epigenetic profile together may improve MPM risk assessment. Above-median asbestos exposure and hypomethylation of cg03546163 in FKBP5 (OR = 20.84, 95% CI = 8.71|53.96, p = 5.5 × 10−11) and hypermethylation of cg06633438 in MLLT1 (OR = 11.71, 95% CI = 4.97|29.64, p = 5.9 × 10−8) genes compared to below-median asbestos exposure and hyper/hypomethylation of single-CpG DNAm, respectively. Receiver Operation Characteristics (ROC) for Case-Control Discrimination showed a significant increase in MPM discrimination when DNAm information was added in the model (baseline model, BM: asbestos exposure, age, gender and white blood cells); area under the ...
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/34071989; info:eu-repo/semantics/altIdentifier/wos/WOS:000659620600001; volume:13; issue:11; firstpage:2636; lastpage:2649; numberofpages:14; journal:CANCERS; http://hdl.handle.net/2318/1801375; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85106609208
DOI: 10.3390/cancers13112636
Availability: http://hdl.handle.net/2318/1801375; https://doi.org/10.3390/cancers13112636
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.E124458B
Database: BASE