Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes

Abstract The main types of thyroid neoplasms, follicular adenoma (FA), follicular thyroid carcinoma (FTC), classical and follicular variants of papillary carcinoma (clPTC and fvPTC), and anaplastic thyroid carcinoma (ATC), differ in prognosis, progression rate and metastatic behaviour. Specific patt...

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Autores principales: Valentina D. Yakushina, Vladimir V. Strelnikov, Alexander S. Tanas, Alexander V. Lavrov
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/72b9d3fe521f46efad58e14192f452eb
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spelling oai:doaj.org-article:72b9d3fe521f46efad58e14192f452eb2021-12-02T15:10:46ZLong noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes10.1038/s41598-021-96149-22045-2322https://doaj.org/article/72b9d3fe521f46efad58e14192f452eb2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-96149-2https://doaj.org/toc/2045-2322Abstract The main types of thyroid neoplasms, follicular adenoma (FA), follicular thyroid carcinoma (FTC), classical and follicular variants of papillary carcinoma (clPTC and fvPTC), and anaplastic thyroid carcinoma (ATC), differ in prognosis, progression rate and metastatic behaviour. Specific patterns of lncRNAs involved in the development of clinical and morphological features can be presumed. LncRNA landscapes within distinct benign and malignant histological variants of thyroid neoplasms were not investigated. The aim of the study was to discover long noncoding RNA landscapes common and specific to major benign and malignant histological subtypes of thyroid neoplasms. LncRNA expression in FA, FTC, fvPTC, clPTC and ATC was analysed with comprehensive microarray and RNA-Seq datasets. Putative biological functions were evaluated via enrichment analysis of coexpressed coding genes. In the results, lncRNAs common and specific to FTC, clPTC, fvPTC, and ATC were identified. The discovered lncRNAs are putatively involved in L1CAM interactions, namely, pre-mRNA processing (lncRNAs specific to FTC); PCP/CE and WNT pathways (lncRNAs specific to fvPTC); extracellular matrix organization (lncRNAs specific to clPTC); and the cell cycle (lncRNAs specific to ATC). Known oncogenic and suppressor lncRNAs (RMST, CRNDE, SLC26A4-AS1, NR2F1-AS1, and LINC00511) were aberrantly expressed in thyroid carcinomas. These findings enhance the understanding of lncRNAs in the development of subtype-specific features in thyroid cancer.Valentina D. YakushinaVladimir V. StrelnikovAlexander S. TanasAlexander V. LavrovNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Valentina D. Yakushina
Vladimir V. Strelnikov
Alexander S. Tanas
Alexander V. Lavrov
Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes
description Abstract The main types of thyroid neoplasms, follicular adenoma (FA), follicular thyroid carcinoma (FTC), classical and follicular variants of papillary carcinoma (clPTC and fvPTC), and anaplastic thyroid carcinoma (ATC), differ in prognosis, progression rate and metastatic behaviour. Specific patterns of lncRNAs involved in the development of clinical and morphological features can be presumed. LncRNA landscapes within distinct benign and malignant histological variants of thyroid neoplasms were not investigated. The aim of the study was to discover long noncoding RNA landscapes common and specific to major benign and malignant histological subtypes of thyroid neoplasms. LncRNA expression in FA, FTC, fvPTC, clPTC and ATC was analysed with comprehensive microarray and RNA-Seq datasets. Putative biological functions were evaluated via enrichment analysis of coexpressed coding genes. In the results, lncRNAs common and specific to FTC, clPTC, fvPTC, and ATC were identified. The discovered lncRNAs are putatively involved in L1CAM interactions, namely, pre-mRNA processing (lncRNAs specific to FTC); PCP/CE and WNT pathways (lncRNAs specific to fvPTC); extracellular matrix organization (lncRNAs specific to clPTC); and the cell cycle (lncRNAs specific to ATC). Known oncogenic and suppressor lncRNAs (RMST, CRNDE, SLC26A4-AS1, NR2F1-AS1, and LINC00511) were aberrantly expressed in thyroid carcinomas. These findings enhance the understanding of lncRNAs in the development of subtype-specific features in thyroid cancer.
format article
author Valentina D. Yakushina
Vladimir V. Strelnikov
Alexander S. Tanas
Alexander V. Lavrov
author_facet Valentina D. Yakushina
Vladimir V. Strelnikov
Alexander S. Tanas
Alexander V. Lavrov
author_sort Valentina D. Yakushina
title Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes
title_short Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes
title_full Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes
title_fullStr Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes
title_full_unstemmed Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes
title_sort long noncoding rna landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/72b9d3fe521f46efad58e14192f452eb
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AT alexanderstanas longnoncodingrnalandscapesspecifictobenignandmalignantthyroidneoplasmsofdistincthistologicalsubtypes
AT alexandervlavrov longnoncodingrnalandscapesspecifictobenignandmalignantthyroidneoplasmsofdistincthistologicalsubtypes
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