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dc.contributor.authorGaluppini, F
dc.contributor.authorCensi, S
dc.contributor.authorMerante Boschin, I
dc.contributor.authorFassan, M
dc.contributor.authorSbaraglia, M
dc.contributor.authorValeri, N
dc.contributor.authorHahne, JC
dc.contributor.authorBertazza, L
dc.contributor.authorMunari, G
dc.contributor.authorGalasso, M
dc.contributor.authorCascione, L
dc.contributor.authorBarollo, S
dc.contributor.authorRugge, M
dc.contributor.authorVianello, F
dc.contributor.authorDei Tos, AP
dc.contributor.authorMian, C
dc.contributor.authorPennelli, G
dc.coverage.spatialSwitzerland
dc.date.accessioned2022-07-12T15:11:53Z
dc.date.available2022-07-12T15:11:53Z
dc.date.issued2022-02-23
dc.identifierARTN 834075
dc.identifier.citationFrontiers in Endocrinology, 2022, 13 pp. 834075 -en_US
dc.identifier.issn1664-2392
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5216
dc.identifier.eissn1664-2392
dc.identifier.eissn1664-2392
dc.identifier.doi10.3389/fendo.2022.834075
dc.description.abstractPapillary thyroid carcinoma (PTC) is a miscellaneous disease with a variety of histological variants, each with its own mutational profile, and clinical and prognostic characteristics. Identification of microRNA (miRNA) expression profiles represents an important benchmark for understanding the molecular mechanisms underlying the biological behavior of these unique PTC subtypes in order that they be better characterized. We considered a series of 35 PTC samples with a histological diagnosis of either hobnail (17 cases) or classical variant (nine cases) and with a specific BRAF p.K601E mutation (nine cases). We determined the overall miRNA expression profile with NanoString technology, and both quantitative reverse transcription-PCR and in situ hybridization were used to confirm selected miRNAs. The miRNA signature was found to consistently differentiate specific histotypes and mutational profiles. In contrast to the BRAF p.K601E mutation and classic PTCs, three miRNAs (miR-21-5p, miR-146b-5p, and miR-205-5p) were substantially overexpressed in the hobnail variant. The current study found that different miRNA signature profiles were linked to unique histological variants and BRAF mutations in PTC. Further studies focusing on the downstream pathogenetic functions of mRNAs in thyroid neoplasms are warranted.
dc.formatElectronic-eCollection
dc.format.extent834075 -
dc.languageeng
dc.language.isoengen_US
dc.publisherFRONTIERS MEDIA SAen_US
dc.relation.ispartofFrontiers in Endocrinology
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectBRAF
dc.subjecthistological variant
dc.subjecthobnail
dc.subjectmiR-146
dc.subjectmiR-205
dc.subjectmiR-21
dc.subjectmicroRNA
dc.subjectpapillary thyroid cancer
dc.subjectCarcinoma, Papillary
dc.subjectHumans
dc.subjectMicroRNAs
dc.subjectProto-Oncogene Proteins B-raf
dc.subjectThyroid Cancer, Papillary
dc.subjectThyroid Neoplasms
dc.titlePapillary Thyroid Carcinoma: Molecular Distinction by MicroRNA Profiling.en_US
dc.typeJournal Article
dcterms.dateAccepted2022-01-26
dc.date.updated2022-07-12T15:11:23Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.3389/fendo.2022.834075en_US
rioxxterms.licenseref.startdate2022-02-23
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35282462
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Gastrointestinal Cancer Biology and Genomics
pubs.publication-statusPublished online
pubs.volume13
icr.researchteamGI Cancer Biol & Genomicsen_US
dc.contributor.icrauthorValeri, Nicola
icr.provenanceDeposited by Mr Arek Surman on 2022-07-12. Deposit type is initial. No. of files: 1. Files: Papillary Thyroid Carcinoma Molecular Distinction by MicroRNA Profiling.pdf


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