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DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions

DGCR8 emerged recently as miRNAs biogenesis pathway protein with a highlighted role in thyroid disease. This study aimed to characterize this miRNA biogenesis component, in particular the p.(E518K) mutation and DGCR8 expression in a series of thyroid lesions. The series of thyroid lesions was genoty...

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Autores principales: Rodrigues, Lia, Canberk, Sule, Macedo, Sofia, Soares, Paula, Vinagre, João
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740158/
https://www.ncbi.nlm.nih.gov/pubmed/36499151
http://dx.doi.org/10.3390/ijms232314812
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author Rodrigues, Lia
Canberk, Sule
Macedo, Sofia
Soares, Paula
Vinagre, João
author_facet Rodrigues, Lia
Canberk, Sule
Macedo, Sofia
Soares, Paula
Vinagre, João
author_sort Rodrigues, Lia
collection PubMed
description DGCR8 emerged recently as miRNAs biogenesis pathway protein with a highlighted role in thyroid disease. This study aimed to characterize this miRNA biogenesis component, in particular the p.(E518K) mutation and DGCR8 expression in a series of thyroid lesions. The series of thyroid lesions was genotyped for the c.1552G>A p.(E518K) mutation. When frozen tissue was available, DGCR8 mRNA expression was analysed by qPCR. Formalin-fixed paraffin-embedded tissues were studied for DGCR8 immunoexpression. We present for the first time the p.(E518K) mutation in a case of poorly differentiated thyroid carcinoma and present the deregulation of DGCR8 expression at mRNA level in follicular-patterned tumours. The obtained data solidify DGCR8 as another important player of miRNA-related gene mutations in thyroid tumorigenesis, particularly in follicular-patterned thyroid tumours.
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spelling pubmed-97401582022-12-11 DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions Rodrigues, Lia Canberk, Sule Macedo, Sofia Soares, Paula Vinagre, João Int J Mol Sci Article DGCR8 emerged recently as miRNAs biogenesis pathway protein with a highlighted role in thyroid disease. This study aimed to characterize this miRNA biogenesis component, in particular the p.(E518K) mutation and DGCR8 expression in a series of thyroid lesions. The series of thyroid lesions was genotyped for the c.1552G>A p.(E518K) mutation. When frozen tissue was available, DGCR8 mRNA expression was analysed by qPCR. Formalin-fixed paraffin-embedded tissues were studied for DGCR8 immunoexpression. We present for the first time the p.(E518K) mutation in a case of poorly differentiated thyroid carcinoma and present the deregulation of DGCR8 expression at mRNA level in follicular-patterned tumours. The obtained data solidify DGCR8 as another important player of miRNA-related gene mutations in thyroid tumorigenesis, particularly in follicular-patterned thyroid tumours. MDPI 2022-11-26 /pmc/articles/PMC9740158/ /pubmed/36499151 http://dx.doi.org/10.3390/ijms232314812 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rodrigues, Lia
Canberk, Sule
Macedo, Sofia
Soares, Paula
Vinagre, João
DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions
title DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions
title_full DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions
title_fullStr DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions
title_full_unstemmed DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions
title_short DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions
title_sort dgcr8 microprocessor subunit mutation and expression deregulation in thyroid lesions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740158/
https://www.ncbi.nlm.nih.gov/pubmed/36499151
http://dx.doi.org/10.3390/ijms232314812
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