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dc.contributor.authorMoon, J.-Y.-
dc.contributor.authorLee, E.J.-
dc.contributor.authorChung, W.Y.-
dc.contributor.authorMoon, M.H.-
dc.contributor.authorChung, B.C.-
dc.contributor.authorChoi, M.H.-
dc.date.accessioned2024-01-20T11:31:59Z-
dc.date.available2024-01-20T11:31:59Z-
dc.date.created2021-09-02-
dc.date.issued2013-10-
dc.identifier.issn1472-6890-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/127633-
dc.description.abstractBackground: Estrogen metabolism may be associated with the pathophysiological development of papillary thyroid carcinoma (PTC). Methods. To evaluate the differential estrogen metabolism between benign and malignant PTCs, estrogen profiling by gas chromatography-mass spectrometry was applied to urine samples from postmenopausal patients with 9 benign tumors and 18 malignant stage I and III/IV PTCs. Results: The urinary concentration of 2-methoxyestradiol was significantly lower in the stage I malignant patients (3.5-fold; P < 0.025) than in the benign group. The metabolic ratios of 16α-OH-estrone/estrone and estriol/estradiol, which are responsible for 16α-hydroxylase activity, were increased more than 2.5-fold in the advanced-stage malignant PTC (P < 0.02 each). The more than 6.2-fold decrease in the urinary 2-/16α-hydroxylase ratio in stage III/IV malignant PTC was consistent with the ratio in postmenopausal patients with endocrine gland cancers. In addition, reductive 17β-hydroxysteroid dehydrogenase (17β-HSD; estradiol/estrone or estriol/16α-OH-estrone) was present at significantly higher levels in subjects with stage III/IV malignant PTCs than in benign subjects (>3.5-fold difference; P < 0.002). In particular, the estriol/16α-OH-estrone ratio differentiated between the benign and early-stage malignant patients (P < 0.01). Conclusions: Increased 16α-hydroxylation and/or a decreased 2-/16α-ratio, as well increased reductive 17β-HSD, with regard to estrogen metabolism could provide potential biomarkers. The devised profiles could be useful for differentiating malignant thyroid carcinomas from benign adenomas in postmenopausal women. ? 2013 Moon et al.; licensee BioMed Central Ltd.-
dc.languageEnglish-
dc.subject16alpha oxygenase-
dc.subject2 methoxyestradiol-
dc.subjectestradiol-
dc.subjectestriol-
dc.subjectestrogen-
dc.subjectestrone-
dc.subjectoxygenase-
dc.subjecttestosterone 17beta dehydrogenase-
dc.subjectunclassified drug-
dc.subjectadult-
dc.subjectarticle-
dc.subjectbenign tumor-
dc.subjectcancer patient-
dc.subjectclinical article-
dc.subjectcontrolled study-
dc.subjectdisease severity-
dc.subjectenzyme activity-
dc.subjectestrogen metabolism-
dc.subjectfemale-
dc.subjecthuman-
dc.subjecthuman tissue-
dc.subjectkidney concentrating capacity-
dc.subjectmass fragmentography-
dc.subjectmetabolic rate-
dc.subjectpostmenopause-
dc.subjectthyroid carcinoma-
dc.subjecturinalysis-
dc.subjecturine level-
dc.titleComparison of metabolic ratios of urinary estrogens between benign and malignant thyroid tumors in postmenopausal women-
dc.typeArticle-
dc.identifier.doi10.1186/1472-6890-13-25-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBMC Clinical Pathology, v.13, no.1-
dc.citation.titleBMC Clinical Pathology-
dc.citation.volume13-
dc.citation.number1-
dc.description.journalRegisteredClassscopus-
dc.identifier.scopusid2-s2.0-84886187680-
dc.type.docTypeArticle-
dc.subject.keywordPlus16alpha oxygenase-
dc.subject.keywordPlus2 methoxyestradiol-
dc.subject.keywordPlusestradiol-
dc.subject.keywordPlusestriol-
dc.subject.keywordPlusestrogen-
dc.subject.keywordPlusestrone-
dc.subject.keywordPlusoxygenase-
dc.subject.keywordPlustestosterone 17beta dehydrogenase-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusbenign tumor-
dc.subject.keywordPluscancer patient-
dc.subject.keywordPlusclinical article-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusdisease severity-
dc.subject.keywordPlusenzyme activity-
dc.subject.keywordPlusestrogen metabolism-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlushuman-
dc.subject.keywordPlushuman tissue-
dc.subject.keywordPluskidney concentrating capacity-
dc.subject.keywordPlusmass fragmentography-
dc.subject.keywordPlusmetabolic rate-
dc.subject.keywordPluspostmenopause-
dc.subject.keywordPlusthyroid carcinoma-
dc.subject.keywordPlusurinalysis-
dc.subject.keywordPlusurine level-
dc.subject.keywordAuthor16α-hydroxylation-
dc.subject.keywordAuthor17β-hydroxysteroid dehydrogenase-
dc.subject.keywordAuthorEstrogens-
dc.subject.keywordAuthorPostmenopause-
dc.subject.keywordAuthorThyroid cancer-
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