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Differential Expression of Glycolysis-Related Proteins in Follicular Neoplasms versus Hürthle Cell Neoplasms: A Retrospective Analysis

DC Field Value Language
dc.contributor.author구자승-
dc.contributor.author김혜민-
dc.date.accessioned2018-07-20T07:37:59Z-
dc.date.available2018-07-20T07:37:59Z-
dc.date.issued2017-
dc.identifier.issn0278-0240-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/160356-
dc.description.abstractPURPOSE: Although currently classified as variants of follicular neoplasms (FNs), Hürthle cell neoplasms (HCNs) exhibit distinct biological characteristics. Hence, the metabolism of both neoplasms may also be different. The aims of this study were to investigate and compare the expression of glycolysis-related proteins in HCNs and FNs and to determine the clinical implications of such expression. METHODS: Tissue microarrays were constructed with 265 samples of FNs (112 follicular carcinomas (FCs) and 153 follicular adenomas (FAs)) as well as 108 samples of HCNs (27 Hürthle cell carcinomas (HCCs) and 81 Hürthle cell adenomas (HCAs)). Immunohistochemical staining for the glycolysis-related molecules Glut-1, hexokinase II, CAIX, and MCT4 was performed. RESULTS: The expression levels of Glut-1, hexokinase II, CAIX, and MCT4 were significantly higher in HCNs than in FNs (p < 0.001). Glut-1, hexokinase II, CAIX, and MCT4 expression levels were highest in HCC, followed by HCA, FC, and FA (all p < 0.001). In HCC, hexokinase II positivity was associated with large tumor size (>4 cm) (p = 0.046), CAIX positivity with vascular invasion (p = 0.005), and MCT4 positivity with extrathyroidal extension (p = 0.030). CONCLUSION: The expression levels of the glycolysis-related proteins Glut-1, hexokinase II, CAIX, and MCT4 were higher in HCNs than in FNs and in HCCs than in HCAs.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherHindawi Pub. Corp.-
dc.relation.isPartOfDISEASE MARKERS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdenoma/genetics-
dc.subject.MESHAdenoma/metabolism*-
dc.subject.MESHAdenoma, Oxyphilic/genetics-
dc.subject.MESHAdenoma, Oxyphilic/metabolism*-
dc.subject.MESHCarbonic Anhydrase IX/genetics-
dc.subject.MESHCarbonic Anhydrase IX/metabolism-
dc.subject.MESHCarcinoma/genetics-
dc.subject.MESHCarcinoma/metabolism*-
dc.subject.MESHFemale-
dc.subject.MESHGlucose Transporter Type 1/genetics-
dc.subject.MESHGlucose Transporter Type 1/metabolism-
dc.subject.MESHGlycolysis*-
dc.subject.MESHHexokinase/genetics-
dc.subject.MESHHexokinase/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMonocarboxylic Acid Transporters/genetics-
dc.subject.MESHonocarboxylic Acid Transporters/metabolism-
dc.subject.MESHMuscle Proteins/genetics-
dc.subject.MESHMuscle Proteins/metabolism-
dc.subject.MESHThyroid Neoplasms/genetics-
dc.subject.MESHThyroid Neoplasms/metabolism*-
dc.titleDifferential Expression of Glycolysis-Related Proteins in Follicular Neoplasms versus Hürthle Cell Neoplasms: A Retrospective Analysis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Pathology-
dc.contributor.googleauthorHye Min Kim-
dc.contributor.googleauthorJa Seung Koo-
dc.identifier.doi10.1155/2017/6230294-
dc.contributor.localIdA00198-
dc.contributor.localIdA04553-
dc.relation.journalcodeJ00743-
dc.identifier.eissn1875-8630-
dc.identifier.pmid28790533-
dc.contributor.alternativeNameKoo, Ja Seung-
dc.contributor.alternativeNameKim, Hye Min-
dc.contributor.affiliatedAuthorKoo, Ja Seung-
dc.contributor.affiliatedAuthorKim, Hye Min-
dc.contributor.affiliatedAuthor구자승-
dc.citation.volume2017-
dc.citation.startPage6230294-
dc.identifier.bibliographicCitationDISEASE MARKERS, Vol.2017 : 6230294, 2017-
dc.identifier.rimsid42088-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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