Thyroid hormone receptors and type I iodothryronine 5′-deiodinase activity of human thyroid adenomas and benign cold nodules

被引:18
作者
Brtko, J
Bobálová, J
Podoba, J
Schmutzler, C
Köhrle, J [1 ]
机构
[1] Univ Wurzburg, Med Poliklin, Klin Forschergrp, D-97070 Wurzburg, Germany
[2] Univ Wurzburg, Med Poliklin, Abt Mol Innere Med, D-97070 Wurzburg, Germany
[3] Slovak Acad Sci, Inst Expt Endocrinol, Bratislava 83306, Slovakia
[4] Postgrad Med Sch, Div Endocrinol & Metab Disorders, Bratislava 83303, Slovakia
关键词
thyroid hormone receptor; type I iodothyronine 5 '-deiodinase; electrophoretic mobility shift assay; human thyroid; toxic adenoma; cold nodule;
D O I
10.1055/s-2002-32147
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The majority of thyroid adenomas are of clonal origin. In a subset of toxic adenomas (TAs) and cold nodules (CNs) activating mutations in the thyrotropin (TSH) receptor or G(s)-alpha gene may explain the altered functions in these benign tumours, The present study was undertaken to investigate the status of functional thyroid hormone receptors, major thyroid hormone signal mediators, in both the human TAs and CNs in comparison with a normal thyroid tissue from the same patient. Electrophoretic mobility shift assays using a DR4 ("direct repeats" 4), a thyroid hormone responsive element (TRE) of human type I iodothyronine 5'-deiodinase demonstrated the DNA-binding of thyroid hormone receptors (TRs) in thyroid tissue nuclear extracts. A significant increase (p < 0.05) in the functional binding properties of TRs to the DR4 thyroid hormone responsive element was found in TAs when compared to normal thyroid tissue. Contrary, a marked diminution in the TR-TRE complex formation was found in CNs in comparison with normal thyroid tissue. In addition, functional activity of the iodothyronine 5'-deiodinase (5'DI) was analyzed in benign tumours, thyroid TAs and CNs in comparison with that of normal thyroid tissue. A significantly increased (p < 0.01) activity of 5'DI was demonstrated in TAs, and in contrast, decreased Values of the enzyme activity were found in CNs when compared to a normal tissue. From the data it is suggested that both the Status of TR-TRE complex formation and the activity of the 5 DI may be altered in benign tumours of human thyroid gland.
引用
收藏
页码:166 / 170
页数:5
相关论文
共 22 条
[1]   A RAPID MICROPREPARATION TECHNIQUE FOR EXTRACTION OF DNA-BINDING PROTEINS FROM LIMITING NUMBERS OF MAMMALIAN-CELLS [J].
ANDREWS, NC ;
FALLER, DV .
NUCLEIC ACIDS RESEARCH, 1991, 19 (09) :2499-2499
[2]   THE IODOTHYRONINE DEIODINASES AND 5'-DEIODINATION [J].
BECKETT, GJ ;
ARTHUR, JR .
BAILLIERES CLINICAL ENDOCRINOLOGY AND METABOLISM, 1994, 8 (02) :285-304
[3]   Constitutive activation of the G(s)alpha protein-adenylate cyclase pathway may not be sufficient to generate toxic thyroid adenomas [J].
Derwahl, M ;
Hamacher, C ;
Russo, D ;
Broecker, M ;
Manole, D ;
Schatz, H ;
Kopp, P ;
Filetti, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (05) :1898-1904
[4]   Molecular aspects of the pathogenesis of nodular goiters, thyroid nodules and adenomas [J].
Derwahl, M .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 1996, 104 :32-35
[5]   THE STEROID AND THYROID-HORMONE RECEPTOR SUPERFAMILY [J].
EVANS, RM .
SCIENCE, 1988, 240 (4854) :889-895
[6]   MOLECULAR-BASIS OF THYROID-CANCER [J].
FARID, NR ;
SHI, YF ;
ZOU, MJ .
ENDOCRINE REVIEWS, 1994, 15 (02) :202-232
[7]  
Gartner R, 1996, EXP CLIN ENDOCR DIAB, V104, P36
[8]   Some new twists in the regulation of gene expression by thyroid hormone and retinoic acid receptors [J].
Glass, CK .
JOURNAL OF ENDOCRINOLOGY, 1996, 150 (03) :349-357
[9]   EXPRESSION OF FUNCTIONAL STIMULATORY GUANINE-NUCLEOTIDE-BINDING PROTEIN IN NONFUNCTIONING THYROID ADENOMAS IS NOT CORRELATED TO ADENYLATE-CYCLASE ACTIVITY AND GROWTH OF THESE TUMORS [J].
HAMACHER, C ;
STUDER, H ;
ZBAEREN, J ;
SCHATZ, H ;
DERWAHL, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (05) :1724-1732
[10]   The promoter of the human type I 5'-deiodinase gene - Mapping of the transcription start site and identification of a DR+4 thyroid-hormone-responsive element [J].
Jakobs, TC ;
Schmutzler, C ;
Meissner, J ;
Kohrle, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 247 (01) :288-297