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Expression of SOX2OT, DANCR and TINCR long non‑coding RNAs in papillary thyroid cancer and its effects on clinicopathological features

dc.contributor.authorIcduygu, Fadime Mutlu
dc.contributor.authorAkgun, Egemen
dc.contributor.authorSengul, Demet
dc.contributor.authorOzgoz, Asuman
dc.contributor.authorAlp, Ebru
dc.date.accessioned2026-01-04T16:30:06Z
dc.date.issued2022-02-10
dc.description.abstractLong non‑coding RNAs (lncRNAs) are molecules that are >200 base pairs long and do not encode a protein. However, they perform important roles in regulating gene expression. Recent studies have revealed that the changes in the expressions of lncRNAs serve a role in the development and metastases of a number of types of cancer. A number of studies have been published on the association of SOX2 overlapping transcript (SOX2OT), differentiation antagonizing non‑protein coding RNA (DANCR) and tissue differentiation‑induced non‑coding RNA (TINCR) expression with various types of cancer. However, researchers have not yet studied their roles in papillary thyroid cancer or at least, those roles are not clarified. The aim of the present study was to investigate the expression and clinical significance of SOX2OT, DANCR and TINCR in papillary thyroid cancer (PTC). A total of 102 patients with PTC were included in the present study. Reverse transcription‑quantitative PCR method was used to determine the relative gene expression levels of lncRNAs and then the relationship between expressions of lncRNAs and clinical characteristics of the subjects was analyzed in detail. Expression levels of SOX2OT (P=0.016) and DANCR (P=0.017) increased in the tumor samples in contrast to the normal tissues. No significant difference was observed in the expression level of TINCR (P=0.298). In addition, SOX2OT expression was associated with micro carcinoma (P<0.001), tumor size (P=0.010) and primary tumor (P=0.006), while DANCR expression was associated with age (P=0.030) and micro carcinoma (P=0.004). The findings of the present study indicated that DANCR may contribute to the development of PTC while SOX2OT may contribute to both the development and progression of PTC.
dc.description.urihttps://doi.org/10.3892/mmr.2022.12636
dc.description.urihttps://www.spandidos-publications.com/10.3892/mmr.2022.12636/download
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/35147200
dc.description.urihttp://dx.doi.org/10.3892/mmr.2022.12636
dc.identifier.doi10.3892/mmr.2022.12636
dc.identifier.eissn1791-3004
dc.identifier.issn1791-2997
dc.identifier.openairedoi_dedup___::dd80766900b41e97e38b6790f145d3a8
dc.identifier.orcid0000-0002-0416-0621
dc.identifier.pubmed35147200
dc.identifier.scopus2-s2.0-105020198799
dc.identifier.urihttps://hdl.handle.net/20.500.12597/39497
dc.identifier.volume25
dc.identifier.wos000759034000001
dc.publisherSpandidos Publications
dc.relation.ispartofMolecular Medicine Reports
dc.rightsOPEN
dc.subjectAdult
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectMale
dc.subjectThyroid Cancer, Papillary
dc.subjectHumans
dc.subjectFemale
dc.subjectRNA, Long Noncoding
dc.subjectArticles
dc.subjectThyroid Neoplasms
dc.subjectMiddle Aged
dc.titleExpression of SOX2OT, DANCR and TINCR long non‑coding RNAs in papillary thyroid cancer and its effects on clinicopathological features
dc.typeArticle
dspace.entity.typePublication
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