001     21893
005     20180210144204.0
024 7 _ |2 pmid
|a pmid:19499989
024 7 _ |2 DOI
|a 10.1007/s12268-012-0207-7
037 _ _ |a PreJuSER-21893
041 _ _ |a eng
082 _ _ |a 570
100 1 _ |a Heck, A.
|b 0
|0 P:(DE-HGF)0
245 _ _ |a Expressionsoptimierung in Mikroorganismen
260 _ _ |a Heidelberg
|b Spektrum
|c 2012
300 _ _ |a 449 - 451
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
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|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Biospektrum
|x 0947-0867
|0 6961
|y 4
|v 18
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Vitamin D receptor (VDR) expression has been shown to be upregulated in several tumors and is supposed to represent an important endogenous response to tumor progression. To investigate the role of the VDR gene and its influence on 25(OH)D(3) and 1,25(OH)(2)D(3) plasma levels in thyroid carcinoma, we analyzed four VDR polymorphisms in patients and healthy controls (HC).Patients with thyroid carcinoma (n = 172) (n = 132 for papillary and n = 40 for follicular) and HC (n = 321) were genotyped for the ApaI (rs7975232), TaqI (rs731236), BsmI (rs1544410), and FokI (rs10735810) polymorphisms within the VDR gene and correlated with 25(OH)D(3) and 1,25(OH)(2)D(3) plasma levels.The genotypes AA of the ApaI (rs7975232) and FF of the FokI (rs10735810) polymorphisms were significantly less frequent (12.5% vs. 35.2% and 25% vs. 42.1%, respectively, both corrected p [p(c)] = 0.04) in patients with follicular thyroid cancer (FTC) than in HC. Additionally, the haplotypes, Ta (57.5% vs. 41.4%; p(c) = 0.0207), af (24.6% vs. 14.3%; p(c) = 0.0116), Tab (51.1% vs. 36.8%; p(c) = 0.0495), and Tabf (18.7% vs. 13.6%; p(c) = 0.0240) were more frequent, whereas the haplotypes AF (17.1% vs. 37.2%; p(c) = 0.0008), BF (11.4% vs. 31.9%; p(c) = 0.012), tF (7.9% vs. 25.5%; p(c) = 0.0016), and tABF (7.6% vs. 23%; p(c) = 0.0115) were less frequent in the FTC patients compared to HC. Neither genotype nor haplotype frequencies differed between patients with papillary thyroid cancer (PTC) and HC. Further, individuals with PTC and FTC had a significantly lower level of circulating 1,25(OH)(2)D(3) compared to controls. In contrast, no differences of the 25(OH)D(3) concentration between patients and HC were observed. VDR polymorphisms were not associated with 25(OH)D(3) and 1,25(OH)(2)D(3) plasma levels.Lower circulating levels of 1,25(OH)(2)D(3) are observed in patients with differentiated thyroid carcinoma. Further, while the alleles AA and FF of the ApaI (rs7975232) and FokI (rs10735810) VDR polymorphisms and the haplotype tABF confer to protection from follicular carcinoma, the haplotype Tabf appeared to be associated with an increased FTC risk. Since this is the first report associating VDR polymorphisms with thyroid carcinoma, these findings need to be confirmed in studies with larger numbers of patients.
536 _ _ |a Biotechnologie
|c PBT
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK410
|x 0
588 _ _ |a Dataset connected to Pubmed
650 _ 2 |2 MeSH
|a Autoantibodies: immunology
650 _ 2 |2 MeSH
|a Calcifediol: metabolism
650 _ 2 |2 MeSH
|a Calcitriol: metabolism
650 _ 2 |2 MeSH
|a Carcinoma, Papillary, Follicular: genetics
650 _ 2 |2 MeSH
|a Carcinoma, Papillary, Follicular: pathology
650 _ 2 |2 MeSH
|a Cell Differentiation
650 _ 2 |2 MeSH
|a Female
650 _ 2 |2 MeSH
|a Genotype
650 _ 2 |2 MeSH
|a Haplotypes
650 _ 2 |2 MeSH
|a Humans
650 _ 2 |2 MeSH
|a Male
650 _ 2 |2 MeSH
|a Neutrophil Infiltration
650 _ 2 |2 MeSH
|a Polymorphism, Genetic: genetics
650 _ 2 |2 MeSH
|a Receptors, Calcitriol: genetics
650 _ 2 |2 MeSH
|a Thyroid Gland: immunology
650 _ 2 |2 MeSH
|a Thyroid Neoplasms: genetics
650 _ 2 |2 MeSH
|a Thyroid Neoplasms: pathology
650 _ 2 |2 MeSH
|a Vitamin D: physiology
650 _ 7 |0 0
|2 NLM Chemicals
|a Autoantibodies
650 _ 7 |0 0
|2 NLM Chemicals
|a Receptors, Calcitriol
650 _ 7 |0 1406-16-2
|2 NLM Chemicals
|a Vitamin D
650 _ 7 |0 19356-17-3
|2 NLM Chemicals
|a Calcifediol
650 _ 7 |0 32222-06-3
|2 NLM Chemicals
|a Calcitriol
700 1 _ |a Tielker, D.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Ernst, J.F.
|b 2
|0 P:(DE-HGF)0
700 1 _ |a Freudl, R.
|b 3
|0 P:(DE-HGF)0
700 1 _ |a Bott, M.
|b 4
|0 P:(DE-HGF)0
700 1 _ |a Oldiges, M.
|b 5
|u FZJ
|0 P:(DE-Juel1)129053
700 1 _ |a Wiechert, W.
|b 6
|u FZJ
|0 P:(DE-Juel1)129076
700 1 _ |a Pietruszka, J.
|b 7
|0 P:(DE-HGF)0
700 1 _ |a Wilhelm, S.
|b 8
|0 P:(DE-HGF)0
700 1 _ |a Rosenau, F.
|b 9
|0 P:(DE-HGF)0
700 1 _ |a Drepper, T.
|b 10
|0 P:(DE-HGF)0
700 1 _ |a Jaeger, K.-E.
|b 11
|0 P:(DE-HGF)0
773 _ _ |a 10.1007/s12268-012-0207-7
|g Vol. 18, p. 449 - 451
|p 449 - 451
|q 18<449 - 451
|0 PERI:(DE-600)2203536-9
|t Biospektrum
|v 18
|y 2012
|x 0947-0867
856 7 _ |u http://dx.doi.org/10.1007/s12268-012-0207-7
909 C O |o oai:juser.fz-juelich.de:21893
|p VDB
913 1 _ |b außerhalb PoF
|k PBT
|l ohne FE
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|v Biotechnologie
|x 0
913 2 _ |a DE-HGF
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|l Key Technologies for the Bioeconomy
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|v Biotechnology
|x 0
914 1 _ |y 2012
915 _ _ |a No Peer Review
|0 StatID:(DE-HGF)0020
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915 _ _ |a DBCoverage
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915 _ _ |a DBCoverage
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920 1 _ |k IBT-2
|l Biotechnologie 2
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|z ab 31.10.10 weitergeführt IBG-1
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|x 0
970 _ _ |a VDB:(DE-Juel1)138049
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)IBG-1-20101118
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBG-1-20101118


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
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