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dc.contributor.author Perge, Pál
dc.contributor.author Decmann, Ábel
dc.contributor.author Pezzani R
dc.contributor.author Bancos I
dc.contributor.author Fassina A
dc.contributor.author Luconi M
dc.contributor.author Canu L
dc.contributor.author Tóth Miklós
dc.contributor.author Boscaro M
dc.contributor.author Patócs Attila
dc.contributor.author Igaz Péter
dc.date.accessioned 2022-06-14T06:52:25Z
dc.date.available 2022-06-14T06:52:25Z
dc.date.issued 2018
dc.identifier 85040085665
dc.identifier journalVolume=59;journalIssueNumber=2;journalTitle=ENDOCRINE;pagerange=280-280;journalAbbreviatedTitle=ENDOCRINE;
dc.identifier.citation journalVolume=59;journalIssueNumber=2;journalTitle=ENDOCRINE;pagerange=280-287;journalAbbreviatedTitle=ENDOCRINE;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/6618
dc.identifier.uri doi:10.1007/s12020-017-1506-z
dc.description.abstract PURPOSE: Circulating microRNAs (miRNA) have been described in patients with adrenocortical tumors, but the expression of miRNAs in non-functioning and cortisol-producing tumors has not been yet compared. Therefore, the objective of this study was to evaluate the expression of plasma extracellular vesicle (EV)-associated microRNAs in patients with non-functioning adrenocortical adenoma (NFA), cortisol-producing adrenocortical adenoma (CPA) and cortisol-producing adrenocortical carcinoma (CP-ACC). METHODS: Preoperative plasma EV samples of 13 NFAs, 13 CPAs and 9 CP-ACCs were subjected to extracellular vesicle isolation. miRNAs were investigated by targeted quantitative real-time PCR normalized to cel-miR-39 as reference. Five miRNAs have been selected for this analysis based on the previous studies including hsa-miR-22-3p, hsa-miR-27a-3p, hsa-miR-210-3p, hsa-miR-320b and hsa-miR-375. RESULTS: We have observed significant overrepresentation of three miRNAs in both CPA and CP-ACC relative to NFA: hsa-miR-22-3p (p < 0.01 and p < 0.0001, respectively), hsa-miR-27a-3p (p < 0.05 in both comparisons) and hsa-miR-320b (p < 0.05 and p < 0.0001, respectively). Hsa-miR-320b has been significantly overrepresented in CP-ACC relative to CPA (p < 0.01). Hsa-miR-210-3p turned out to be significantly overrepresented only in CP-ACC compared to NFA (p < 0.05). Significant correlation was revealed between circulating miRNA concentrations and urinary free cortisol values for hsa-miR-22-3p, hsa-miR-27a-3p and hsa-miR-320b (p < 0.0001 for all) and cortisol after low-dose dexamethasone test for hsa-miR-22-3p and hsa-miR-320b (p < 0.05). Hsa-miR-27a-3p has been significantly stimulated by low-dose dexamethasone test (p < 0.05). CONCLUSIONS: EV-associated miRNAs are differentially expressed in different non-functioning and cortisol-producing adrenocortical tumors.
dc.format.extent 280-287
dc.relation.ispartof urn:issn:1355-008X
dc.title Analysis of circulating extracellular vesicle-associated microRNAs in cortisol-producing adrenocortical tumors
dc.date.updated 2018-12-24T20:02:36Z
dc.rights.holder NULL
dc.identifier.mtmt 3311914
dc.identifier.wos 000423837400006
dc.identifier.pubmed 29299796
dc.contributor.institution MTA-SE Molekuláris Medicina Kutatócsoport (2006-ig: MTA-SE Gastroenterológiai és Endocrinológiai Kutatócsoport)
dc.contributor.institution MTA-SE Lendület Örökletes Endokrin Daganatok Kutatócsoport
dc.contributor.institution II. Sz. Belgyógyászati Klinika
dc.contributor.institution Laboratóriumi Medicina Intézet
dc.contributor.institution Doktori Iskola
dc.contributor.institution MTA-SE Gyulladásbiológiai és Immungenomikai Kutatócsoport (2006-ig: MTA-SE Molekuláris Immunológiai Kutatócsoport)


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