Clinical, Biochemical, and Morphological Correlates in Patients Bearing Growth Hormone-Secreting Pituitary Tumors with or without Constitutively Active Adenylyl Cyclase

腺苷酸环化酶 内科学 内分泌学 生长抑素 肢端肥大症 Gsα亚单位 生物 阿德西9 垂体瘤 基础(医学) 激素 医学 刺激 生长激素 胰岛素
作者
Anna Spada,Maura Arosio,D. Bochicchio,Nicoletta Bazzoni,Lucia Vallar,M. Bassetti,G. Faglia
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [Oxford University Press]
卷期号:71 (6): 1421-1426 被引量:291
标识
DOI:10.1210/jcem-71-6-1421
摘要

Somatic mutations in the alpha-chain (alpha s) 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.

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