HUMAN THYROTROPIN RECEPTOR GENE - EXPRESSION IN THYROID-TUMORS AND CORRELATION TO MARKERS OF THYROID DIFFERENTIATION AND DEDIFFERENTIATION

被引:129
作者
BRABANT, G
MAENHAUT, C
KOHRLE, J
SCHEUMANN, G
DRALLE, H
HOANGVU, C
HESCH, RD
VONZURMUHLEN, A
VASSART, G
DUMONT, JE
机构
[1] HANOVER MED SCH,DEPT SURG,W-3000 HANNOVER 61,GERMANY
[2] FREE UNIV BRUSSELS,FAC MED,DEPT INTERDISCIPLINARY RES,B-1050 BRUSSELS,BELGIUM
关键词
THYROTROPIN RECEPTOR; THYROGLOBULIN; THYROID PEROXIDASE; C-MYC; BETA-ACTIN; MESSENGER-RNA EXPRESSION; THYROID CARCINOMA; HYPERFUNCTIONING ADENOMA;
D O I
10.1016/0303-7207(91)90018-N
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Human thyrotropin (TSH) receptor steady-state transcript levels were analyzed by Northern blot analysis in thyroids of patients with thyroid carcinoma, with hyperfunctioning adenoma and in normal controls. In control tissue and benign tumors expression levels of TSH receptor mRNA were high whereas in anaplastic carcinomas no normal TSH receptor mRNA was detected. In papillary and follicular tumors it varied from normal to markedly reduced levels. Thyroid peroxidase (TPO) and thyroglobulin (Tg) mRNA were strongly expressed in normal tissue and in hyperfunctioning adenomas but were completely lost in all anaplastic tumors. In papillary tumors expression of TPO and Tg mRNA varied from normal to a complete loss of expression of either TPO, Tg or both. Tg and TPO steady-state expression did not correlate to TSH receptor transcript levels. C-myc mRNA was highly expressed in anaplastic carcinomas, very variable in normal controls and in differentiated thyroid tumors and low in hyperfunctioning adenomas. In summary, TSH receptor mRNA is persistently expressed in all differentiated thyroid tissues and tumors but lost in undifferentiated carcinomas. Its persistence far along the transformation pathway further supports the concept that this gene which inserts the thyrocytes in the physiological regulatory network is almost consitutively expressed in this cell.
引用
收藏
页码:R7 / R12
页数:6
相关论文
共 35 条
[1]
EXPRESSION OF ONCOGENES IN THYROID-TUMORS - COEXPRESSION OF C-ERBB2/NEU AND C-ERBB [J].
AASLAND, R ;
LILLEHAUG, JR ;
MALE, R ;
JOSENDAL, O ;
VARHAUG, JE ;
KLEPPE, K .
BRITISH JOURNAL OF CANCER, 1988, 57 (04) :358-363
[2]
THYROTROPIN (TSH) RECEPTOR AND ADENYLATE-CYCLASE ACTIVITY IN HUMAN THYROID-TUMORS - ABSENCE OF HIGH-AFFINITY RECEPTOR AND LOSS OF TSH RESPONSIVENESS IN UNDIFFERENTIATED THYROID-CARCINOMA [J].
ABE, Y ;
ICHIKAWA, Y ;
MURAKI, T ;
ITO, K ;
HOMMA, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1981, 52 (01) :23-28
[3]
NEOPLASTIC TRANSFORMATION INACTIVATES SPECIFIC TRANS-ACTING FACTOR(S) REQUIRED FOR THE EXPRESSION OF THE THYROGLOBULIN GENE [J].
AVVEDIMENTO, VE ;
MUSTI, A ;
FUSCO, A ;
BONAPACE, MJ ;
DILAURO, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (06) :1744-1748
[4]
BERGELEFRANC JL, 1985, CANCER, V56, P345, DOI 10.1002/1097-0142(19850715)56:2<345::AID-CNCR2820560224>3.0.CO
[5]
2-O
[6]
THYROTROPIN RECEPTOR GENE-EXPRESSION IN ONCOGENE-TRANSFECTED RAT-THYROID CELLS - CORRELATION BETWEEN TRANSFORMATION, LOSS OF THYROTROPIN-DEPENDENT GROWTH, AND LOSS OF THYROTROPIN RECEPTOR GENE-EXPRESSION [J].
BERLINGIERI, MT ;
AKAMIZU, T ;
FUSCO, A ;
GRIECO, M ;
COLLETTA, G ;
CIRAFICI, AM ;
IKUYAMA, S ;
KOHN, LD ;
VECCHIO, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (01) :172-178
[7]
CLONING OF HUMAN THYROGLOBULIN COMPLEMENTARY-DNA [J].
BROCAS, H ;
CHRISTOPHE, D ;
POHL, V ;
VASSART, G .
FEBS LETTERS, 1982, 137 (02) :189-192
[8]
Burman K D, 1987, Horm Metab Res Suppl, V17, P63
[9]
HUMAN THYROID-CANCER - MEMBRANE THYROTROPIN BINDING AND ADENYLATE-CYCLASE ACTIVITY [J].
CARAYON, P ;
THOMASMORVAN, C ;
CASTANAS, E ;
TUBIANA, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1980, 51 (04) :915-920
[10]
CELL-KINETICS, DNA CONTENT AND TSH RECEPTOR-ADENYLATE CYCLASE SYSTEM IN DIFFERENTIATED THYROID-CANCER [J].
CHANG, TC ;
KUO, SH ;
LIAW, KY ;
CHANG, CC ;
CHEN, FW .
CLINICAL ENDOCRINOLOGY, 1988, 29 (05) :477-484