CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL CORRELATES IN PATIENTS BEARING GROWTH HORMONE-SECRETING PITUITARY-TUMORS WITH OR WITHOUT CONSTITUTIVELY ACTIVE ADENYLYL CYCLASE

被引:253
作者
SPADA, A
AROSIO, M
BOCHICCHIO, D
BAZZONI, N
VALLAR, L
BASSETTI, M
FAGLIA, G
机构
[1] UNIV MILAN, SCI INST SAN RAFFAELE, I-20122 MILAN, ITALY
[2] UNIV MILAN, CTR CYTOPHARMACOL, DEPT PHARMACOL, I-20122 MILAN, ITALY
关键词
D O I
10.1210/jcem-71-6-1421
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Somatic mutations in the α-chain (αs) of the stimulatory regulatory protein of adenylyl cyclase (Gs) causing constitutive activation of the enzyme have been identified in a subset of human GH-secreting pituitary adenomas. This study reports on the differences between acromegalic patients bearing tumors without (group 1; n = 51) or with (group 2; n = 29) this alteration. No difference in age, sex, clinical features, duration of the disease, or cure rate was observed between the two groups. By contrast, group 2 patients had higher basal GH levels than group 1. Moreover, a significant difference in sellar morphology was found; group 2 patients more frequently showed sellas of normal size (grade I) than group 1. Hypersecretory activity of group 2 tumors was also apparent at electron microscopy; contrary to those of group 1, cells of group 2 tumors were densely granulated and showed prominent rough endoplasmic reticulum and Golgi complex. With respect to group 1, group 2 patients were less responsive to GH-releasing hormone, while they were more sensitive to somatostatin- and dopamine-induced GH inhibition. These results suggest that patients with constitutively active adenylyl cyclase have hyperactive tumors; the sensitivity of these tumors to inhibitory agents (somatostatin and dopamine), possibly counteracting the expression of activating mutations, might explain the low rate of tumor growth. © 1990 by The Endocrine Society.
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页码:1421 / 1426
页数:6
相关论文
共 30 条
[1]   CLINICAL USE OF PRESURGICAL AND POSTSURGICAL EVALUATION OF ABNORMAL GH RESPONSES IN ACROMEGALY [J].
AROSIO, M ;
GIOVANELLI, MA ;
RIVA, E ;
NAVA, C ;
AMBROSI, B ;
FAGLIA, G .
JOURNAL OF NEUROSURGERY, 1983, 59 (03) :402-408
[2]  
BARBACID M, 1987, ANNU REV BIOCHEM, V56, P776
[3]   MORPHOLOGICAL-STUDIES ON MIXED GROWTH-HORMONE (GH) AND PROLACTIN (PRL) SECRETING HUMAN PITUITARY-ADENOMAS - COEXISTENCE OF GH AND PRL IN THE SAME SECRETORY GRANULE [J].
BASSETTI, M ;
SPADA, A ;
AROSIO, M ;
VALLAR, L ;
BRINA, M ;
GIANNATTASIO, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 62 (06) :1093-1100
[4]   STIMULATION OF ADENOSINE-3',5'-MONOPHOSPHATE PRODUCTION BY GROWTH HORMONE-RELEASING FACTOR AND ITS INHIBITION BY SOMATOSTATIN IN ANTERIOR-PITUITARY CELLS-INVITRO [J].
BILEZIKJIAN, LM ;
VALE, WW .
ENDOCRINOLOGY, 1983, 113 (05) :1726-1731
[5]   GROWTH HORMONE-RELEASING FACTOR STIMULATES PROLIFERATION OF SOMATOTROPHS INVITRO [J].
BILLESTRUP, N ;
SWANSON, LW ;
VALE, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (18) :6854-6857
[6]   GROWTH HORMONE-RELEASING FACTOR INDUCES C-FOS EXPRESSION IN CULTURED PRIMARY PITUITARY-CELLS [J].
BILLESTRUP, N ;
MITCHELL, RL ;
VALE, W ;
VERMA, IM .
MOLECULAR ENDOCRINOLOGY, 1987, 1 (04) :300-305
[7]   GTP-BINDING PROTEINS - ONE MOLECULAR MACHINE CAN TRANSDUCE DIVERSE SIGNALS [J].
BOURNE, HR .
NATURE, 1986, 321 (6073) :814-816
[8]   G-PROTEIN SUBUNITS - WHO CARRIES WHAT MESSAGE [J].
BOURNE, HR .
NATURE, 1989, 337 (6207) :504-505
[9]  
CLEMENTI E, 1990, ONCOGENE, V5, P1059
[10]  
Diamond L, 1980, Adv Cancer Res, V32, P1, DOI 10.1016/S0065-230X(08)60360-7