Expression of the cholecystokinin2-receptor in normal human thyroid gland and medullary thyroid carcinoma

被引:24
作者
Bläker, M
de Weerth, A
Tometten, M
Schulz, M
Höppner, W
Arlt, D
Cuong, HV
Dralle, H
Terpe, H
Jonas, L
von Schrenck, T
机构
[1] Univ Klinikum Hamburg Eppendorf, Med Kernklin & Poliklin, D-20246 Hamburg, Germany
[2] Inst Hormon & Fortpflanzungsforsch, Hamburg, Germany
[3] Univ Klin Allgemeinchirurg, Halle Saale, Germany
[4] Univ Rostock, Inst Pathol, Rostock, Germany
关键词
D O I
10.1530/eje.0.1460089
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The cholecystokinin2-receptor (CCK2R) promotes secretion and cell growth induced by its ligands cholecystokinin (CCK) and gastrin. The receptor has recently been shown to be expressed in human medullary thyroid carcinomas (MTCs). The objective of this study was to analyze CCK2R expression in MTC samples of different tumor stages as well as in non-malignant thyroid tissues. Design and Methods: Using RT-PCR we investigated 19 MTC samples and TT-cells (a human MTC cell line), as well as samples of normal thyroid. In addition, we performed immumohistochemistry using calcitonin- and CCK2R-specific antibodies on MTCs and samples of C-cell hyperplasia. Results: We demonstrate for the first time that CCK2R is expressed not only in MTCs but in all samples of normal thyroid tissue. Using inummohistochemistry the receptor could be localized on calcitonin-secreting C-cells. The highest incidence of CCK2R expression in MTCs was observed in early-tumor stages, whereas CCK2R could not be detected in advanced or metastasized tumors. Conclusions: The expression of CCK2R in C-cells suggests a physiological function for gastrin and/or CCK in the regulation of calcitonin release, presumably related to bone and calcium metabolism. Moreover, these ligands might act as growth factors in MTCs. Efforts in the development of CCK2R scintigraphy for the detection of MTC lesions might have to consider a lower incidence of the receptor in advanced tumor stages.
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页码:89 / 96
页数:8
相关论文
共 43 条
[21]   Gastrin deficiency results in altered gastric differentiation and decreased colonic proliferation in mice [J].
Koh, TJ ;
Goldenring, JR ;
Ito, S ;
Mashimo, H ;
Kopin, AS ;
Varro, A ;
Dockray, GJ ;
Wang, TC .
GASTROENTEROLOGY, 1997, 113 (03) :1015-1025
[22]   EXPRESSION CLONING AND CHARACTERIZATION OF THE CANINE PARIETAL-CELL GASTRIN RECEPTOR [J].
KOPIN, AS ;
LEE, YM ;
MCBRIDE, EW ;
MILLER, LJ ;
LU, M ;
LIN, HY ;
KOLAKOWSKI, LF ;
BEINBORN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (08) :3605-3609
[23]   Cholecystokinin receptor imaging using an octapeptide DTPA-CCK analogue in patients with medullary thyroid carcinoma [J].
Kwekkeboom, DJ ;
Bakker, WH ;
Kooij, PPM ;
Erion, J ;
Srinivasan, A ;
de Jong, M ;
Reubi, JC ;
Krenning, EP .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 2000, 27 (09) :1312-1317
[24]   INVIVO SOMATOSTATIN RECEPTOR IMAGING IN MEDULLARY-THYROID CARCINOMA [J].
KWEKKEBOOM, DJ ;
REUBI, JC ;
LAMBERTS, SWJ ;
BRUINING, HA ;
MULDER, AH ;
OEI, HY ;
KRENNING, EP .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 76 (06) :1413-1417
[25]   Abnormal gastric histology and decreased acid production in cholecystokinin-B/gastrin receptor-deficient mice [J].
Langhans, N ;
Rindi, G ;
Chiu, M ;
Rehfeld, JF ;
Ardman, B ;
Beinborn, M ;
Kopin, AS .
GASTROENTEROLOGY, 1997, 112 (01) :280-286
[26]  
LEE YM, 1993, J BIOL CHEM, V268, P8164
[27]   C-CELL HYPERPLASIA OF THE THYROID IN A PATIENT WITH GOITROUS HYPOTHYROIDISM AND HASHIMOTOS THYROIDITIS [J].
LIBBEY, NP ;
NOWAKOWSKI, KJ ;
TUCCI, JR .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1989, 13 (01) :71-77
[28]   The identification of false positive responses to the pentagastrin stimulation test in RET mutation negative members of MEN 2A families [J].
Marsh, DJ ;
McDowall, D ;
Hyland, VJ ;
Andrew, SD ;
Schnitzler, M ;
Gaskin, EL ;
Nevell, DF ;
Diamond, T ;
Delbridge, L ;
CliftonBligh, P ;
Robinson, BG .
CLINICAL ENDOCRINOLOGY, 1996, 44 (02) :213-220
[29]   Coexpression of gastrin and gastrin receptors (CCK-B and ΔCCK-B) in gastrointestinal tumour cell lines [J].
McWilliams, DF ;
Watson, SA ;
Crosbee, DM ;
Michaeli, D ;
Seth, R .
GUT, 1998, 42 (06) :795-798
[30]   The gastric enterochromaffin-like cell: An enigmatic cellular link [J].
Modlin, IM ;
Tang, LH .
GASTROENTEROLOGY, 1996, 111 (03) :783-810