DataSheet_1_Circulating Levels of MiRNAs From 320 Family in Subjects With Lipodystrophy: Disclosing Novel Signatures of the Disease.docx

التفاصيل البيبلوغرافية
العنوان: DataSheet_1_Circulating Levels of MiRNAs From 320 Family in Subjects With Lipodystrophy: Disclosing Novel Signatures of the Disease.docx
المؤلفون: Alessia Dattilo, Giovanni Ceccarini, Gaia Scabia, Silvia Magno, Lara Quintino, Caterina Pelosini, Guido Salvetti, Roberto Cusano, Matteo Massidda, Lucia Montanelli, Donatella Gilio, Gianluca Gatti, Alessandro Giacomina, Mario Costa, Ferruccio Santini, Margherita Maffei
سنة النشر: 2022
المجموعة: Frontiers: Figshare
مصطلحات موضوعية: Endocrinology, Reproduction, Cell Metabolism, lipodystrophy subtypes, miRNA, metabolism, gene ontology, circulating biomarker, kobberling
الوصف: Lipodystrophy (LD) indicates a group of rare disorders, with generalized or partial loss of white adipose tissue (WAT) often associated with metabolic derangements. Heterogeneity/wide spectrum of the disease and lack of biomarkers make diagnosis often difficult. MicroRNAs are important to maintain a correct WAT function and WAT is a source of circulating miRNAs (cmiRs). miRNAs from 320 family were previously detected in the WAT and variably associated to the metabolic syndrome. Our aim was then to investigate if LD can result in altered abundance of cmiRs-320. We collected samples from a cohort of LD subjects of various subtypes and from age matched controls. Use of quantitative PCR determined that cmiRs- 320a-3p, 320b, 320c, 320e are upregulated, while 320d is downregulated in LD. CmiRs-320 power as classifiers was more powerful in the most extreme and defined forms of LD, including the generalized and the Dunnigan subtypes. cmiR-320a-3p showed significant inverse relationships with plasma leptin (P < 0.0001), typically low in LD. The hepatic enzymes gamma-glutamyl transferase (GGT), aspartate aminotransferase (AST), alanine aminotransferase (ALT) and the marker of inflammation C-reactive protein (CRP) were inversely related to cmiR 320d (P < 0.05, for CRP and GGT; P < 0.01, for AST and ALT). Gene ontology analysis revealed cell-cell adhesion as a process regulated by 320 miRNAs targets, thus disclosing a novel route to investigate origin of WAT loss/dysfunction. In conclusion, cmiRs-320 constitute novel biomarkers of LD, abundance of miR320a-3p is inversely associated to indicators related to WAT function, while downregulation of cmiR-320d predicts an altered hepatic profile and higher inflammation.
نوع الوثيقة: dataset
اللغة: unknown
العلاقة: https://figshare.com/articles/dataset/DataSheet_1_Circulating_Levels_of_MiRNAs_From_320_Family_in_Subjects_With_Lipodystrophy_Disclosing_Novel_Signatures_of_the_Disease_docx/20001854Test
DOI: 10.3389/fendo.2022.866679.s001
الإتاحة: https://doi.org/10.3389/fendo.2022.866679.s001Test
https://figshare.com/articles/dataset/DataSheet_1_Circulating_Levels_of_MiRNAs_From_320_Family_in_Subjects_With_Lipodystrophy_Disclosing_Novel_Signatures_of_the_Disease_docx/20001854Test
حقوق: CC BY 4.0
رقم الانضمام: edsbas.B4801CF6
قاعدة البيانات: BASE