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Expression Patterns of Glucose Transporter-1 Gene and Thyroid Specific Genes in Human Papillary Thyroid Carcinoma

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dc.contributor.authorKim, S.-
dc.contributor.authorChung, J.-K.-
dc.contributor.authorMin, H.-S.-
dc.contributor.authorKang, J.-H.-
dc.contributor.authorPark, D.J.-
dc.contributor.authorJeong, J.M.-
dc.contributor.authorLee, D.S.-
dc.contributor.authorPark, S.-H.-
dc.contributor.authorCho, B.Y.-
dc.contributor.authorLee, S.-
dc.contributor.authorLee, M.C.-
dc.date.accessioned2021-09-05T15:51:54Z-
dc.date.available2021-09-05T15:51:54Z-
dc.date.created2021-06-17-
dc.date.issued2014-
dc.identifier.issn1869-3474-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/100684-
dc.description.abstractPurpose: The expression of glucose transporter-1 (Glut-1) gene and those of major thyroid-specific genes were examined in papillary carcinoma tissues, and the expressions of these genes were compared with cancer differentiation grades. Materials and Methods: Twenty-four human papillary carcinoma tissues were included in this study. The expressions of Glut-1- and thyroid-specific genes [sodium/iodide symporter (NIS), thyroid peroxidase, thyroglobulin, TSH receptor and pendrin] were analyzed by RT-PCR. Expression levels were expressed as ratios versus the expression of beta-actin. Pathologic differentiation of papillary carcinoma was classified into a relatively well-differentiated group (n = 13) and relatively less differentiated group (n = 11). Results: Glut-1 gene expression was significantly higher in the less differentiated group (0.66 ± 0.04) than in the well-differentiated group (0.59 ± 0.07). The expression levels of the NIS, PD and TG genes were significantly higher in the well-differentiated group (NIS: 0.67 ± 0.20, PD: 0.65 ± 0.21, TG: 0.74 ± 0.16) than in the less differentiated group (NIS: 0.36 ± 0.05, PD: 0.49 ± 0.08, TG: 0.60 ± 0.11), respectively. A significant negative correlation was found between Glut-1 and NIS expression, and positive correlations were found between NIS and TG, and between NIS and PD. Conclusion: The NIS, PD and TG genes were highly expressed in well-differentiated thyroid carcinomas, whereas the Glut-1 gene was highly expressed in less differentiated thyroid carcinomas. These findings provide a molecular rationale for the management of papillary carcinoma, especially in the selection of FDG PET or radioiodine whole-body scan and I-131-based therapy. © 2014 Korean Society of Nuclear Medicine.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSpringer Verlag-
dc.subjectglucose transporter 1-
dc.subjectpendrin-
dc.subjectsodium iodide symporter-
dc.subjectthyroglobulin-
dc.subjectthyroid peroxidase-
dc.subjectthyrotropin receptor-
dc.subjectarticle-
dc.subjectclinical article-
dc.subjectcontrolled study-
dc.subjectdensitometry-
dc.subjectgene expression-
dc.subjecthistopathology-
dc.subjecthuman-
dc.subjecthuman tissue-
dc.subjectpriority journal-
dc.subjectreverse transcription polymerase chain reaction-
dc.subjectthyroid carcinoma-
dc.subjecttumor differentiation-
dc.titleExpression Patterns of Glucose Transporter-1 Gene and Thyroid Specific Genes in Human Papillary Thyroid Carcinoma-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, S.-
dc.identifier.doi10.1007/s13139-013-0249-x-
dc.identifier.scopusid2-s2.0-84901306745-
dc.identifier.bibliographicCitationNuclear Medicine and Molecular Imaging, v.48, no.2, pp.91 - 97-
dc.relation.isPartOfNuclear Medicine and Molecular Imaging-
dc.citation.titleNuclear Medicine and Molecular Imaging-
dc.citation.volume48-
dc.citation.number2-
dc.citation.startPage91-
dc.citation.endPage97-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001882119-
dc.description.journalClass1-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPlusglucose transporter 1-
dc.subject.keywordPluspendrin-
dc.subject.keywordPlussodium iodide symporter-
dc.subject.keywordPlusthyroglobulin-
dc.subject.keywordPlusthyroid peroxidase-
dc.subject.keywordPlusthyrotropin receptor-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusclinical article-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusdensitometry-
dc.subject.keywordPlusgene expression-
dc.subject.keywordPlushistopathology-
dc.subject.keywordPlushuman-
dc.subject.keywordPlushuman tissue-
dc.subject.keywordPluspriority journal-
dc.subject.keywordPlusreverse transcription polymerase chain reaction-
dc.subject.keywordPlusthyroid carcinoma-
dc.subject.keywordPlustumor differentiation-
dc.subject.keywordAuthorGlucose transporter-1-
dc.subject.keywordAuthorPapillary thyroid cancer-
dc.subject.keywordAuthorPendrin-
dc.subject.keywordAuthorSodium/iodide symporter-
dc.subject.keywordAuthorThyroglobulin-
dc.subject.keywordAuthorThyroid peroxidase-
dc.subject.keywordAuthorTSH receptor-
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