Endocrine Reviews · 2001 · 324 citations · 353 references
MedicineEndocrinologyPharmacologyCell SignalingReproductive EndocrinologySteroid BiochemistryAdrenal DisordersAdrenal EndocrinologyAdrenal HormonesAdrenal Steroid HormonesAdrenal SteroidogenesisAdrenal TumorsAdrenal PathophysiologyAdrenal Steroid ReceptorsCushing Syndrome PathophysiologyGastric Inhibitory Polypeptide SignalingHormone-producing TumorsMembrane Hormone ReceptorsMembrane-bound Hormone ReceptorsReceptors
The mechanism by which cortisol is produced in adrenal Cushing's syndrome, when ACTH is suppressed, was previously unknown and was referred to as being "autonomous." More recently, several investigators have shown that some cortisol and other steroid-producing adrenal tumors or hyperplasias are under the control of ectopic (or aberrant, illicit, inappropriate) membrane hormone receptors. These include ectopic receptors for gastric inhibitory polypeptide (GIP), -adrenergic agonists, or LH/hCG; a similar outcome can result from altered activity of eutopic receptors, such as those for vasopressin (V1-AVPR), serotonin (5-HT 4 ), or possibly leptin. The presence of aberrant receptors places adrenal cells under stimulation by a trophic factor not negatively regulated by glucocorticoids, leading to in-creased steroidogenesis and possibly to the proliferative phenotype. The molecular mechanisms responsible for the abnormal expression and function of membrane hormone receptors are still largely unknown. Identification of the presence of these illicit receptors can eventually lead to new pharmacological therapies as alternatives to adrenalectomy, now demonstrated by the long-term control of ectopic -ARand LH/hCGR-dependent Cushing's syndrome by propanolol and leuprolide acetate. Further studies will potentially identify a larger diversity of hormone receptors capable of coupling to G proteins, adenylyl cyclase, and steroidogenesis in functional adrenal tumors and probably in other endocrine and nonendocrine tumors. (Endocrine Reviews 22: 75-110, 2001) I. Introduction II. Hormonal Regulation of the Normal Adrenal Cortex III. Primary Adrenal Cushing's Syndrome (CS) IV. Initial in Vitro Evidence of Ectopic Adrenal Membrane Hormone Receptors V. In Vivo Demonstration of the Functionality of Ectopic or Abnormal Membrane Hormone Receptors A. Food-and GIP-dependent CS B. Vasopressin-responsive CS C. Catecholamine-dependent CS D. LH-dependent CS E. LH-dependent adrenal androgen-secreting tumors F. Serotonin-responsive CS G. Steroid-responsive CS H. Other abnormal hormone responses in adrenal CS VI. Investigation Strategy A. Initial clinical screening protocol B. Further characterization of abnormal hormone receptors C. Systematic clinical screening for ectopic/abnormal hormone receptors VII. Molecular Mechanisms of Ectopic/Abnormal Hormone Receptors A. Tissue-specific expression and regulation of membrane hormone receptors B. Potential mechanisms of ectopic or abnormal hormone receptors C. Role of ectopic hormone receptors in adrenocortical cell proliferation VIII. Ectopic/Abnormal
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