Literature DB >> 12519861

Overexpression of serotonin4 receptors in cisapride-responsive adrenocorticotropin-independent bilateral macronodular adrenal hyperplasia causing Cushing's syndrome.

Dorthe Cartier1, Isabelle Lihrmann, Françoise Parmentier, Christian Bastard, Jérôme Bertherat, Philippe Caron, Jean-Marc Kuhn, André Lacroix, Antoine Tabarin, Jacques Young, Hubert Vaudry, Hervé Lefebvre.   

Abstract

The serotonin4 (5-HT4) receptor agonists cisapride and/or metoclopramide have been shown to stimulate cortisol secretion in some patients with ACTH-independent bilateral macronodular adrenal hyperplasias (AIMAH) causing Cushing's syndrome. In the present study, we have investigated quantitatively and qualitatively the expression of the 5-HT4 receptor in both normal adrenal cortex and tissues removed from six patients (P1-P6) with cisapride-responsive AIMAH and Cushing's syndrome. Real-time quantitative PCR assay revealed that the 5-HT4 receptor was overexpressed in four of the six hyperplasias studied when compared with normal adrenal cortex. In these tissues, 5-HT4 receptor mRNA expression was 3 to 16 times higher than in normal glands, likely explaining the abnormal in vivo cortisol response to cisapride. Characterization of 5-HT4 receptor splice variants by RT-PCR in both hyperplastic and normal adrenals showed that the variants present in the two hyperplasias that did not overexpress the 5-HT4 receptor, i.e. P2 and P5, could also be detected in the normal adrenal tissue. In addition, sequencing of the full-length cDNAs encoding 5-HT4 receptors in hyperplasias P2 and P5 did not reveal any mutation. Taken together, our results show an overexpression of the 5-HT4 receptor in cisapride-responsive AIMAH. However, in two cases, the level of expression of the receptor in the hyperplastic adrenal cortex was similar to that of normal adrenal gland. The enhanced sensitivity of these two tissues to 5-HT4 receptor agonists was not due to ectopic expression of 5-HT4 receptor isoforms or to the occurrence of somatic gain-of-function mutation of the receptor.

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Year:  2003        PMID: 12519861     DOI: 10.1210/jc.2002-021107

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  13 in total

Review 1.  Aberrant expression of hormone receptors in adrenal Cushing's syndrome.

Authors:  Stavroula Christopoulos; Isabelle Bourdeau; André Lacroix
Journal:  Pituitary       Date:  2004       Impact factor: 4.107

2.  Phosphodiesterase 11A (PDE11A) gene defects in patients with acth-independent macronodular adrenal hyperplasia (AIMAH): functional variants may contribute to genetic susceptibility of bilateral adrenal tumors.

Authors:  Delphine Vezzosi; Rossella Libé; Camille Baudry; Marthe Rizk-Rabin; Anelia Horvath; Isaac Levy; Fernande René-Corail; Bruno Ragazzon; Constantine A Stratakis; Grégoire Vandecasteele; Jérôme Bertherat
Journal:  J Clin Endocrinol Metab       Date:  2012-09-20       Impact factor: 5.958

Review 3.  Update on primary bilateral macronodular adrenal hyperplasia (PBMAH).

Authors:  Lucas Bouys; Iacopo Chiodini; Wiebke Arlt; Martin Reincke; Jérôme Bertherat
Journal:  Endocrine       Date:  2021-02-15       Impact factor: 3.633

Review 4.  Primary bilateral macronodular adrenal hyperplasia: definitely a genetic disease.

Authors:  Isadora P Cavalcante; Annabel Berthon; Maria C Fragoso; Martin Reincke; Constantine A Stratakis; Bruno Ragazzon; Jérôme Bertherat
Journal:  Nat Rev Endocrinol       Date:  2022-08-03       Impact factor: 47.564

5.  PKA regulatory subunit 1A inactivating mutation induces serotonin signaling in primary pigmented nodular adrenal disease.

Authors:  Zakariae Bram; Estelle Louiset; Bruno Ragazzon; Sylvie Renouf; Julien Wils; Céline Duparc; Isabelle Boutelet; Marthe Rizk-Rabin; Rossella Libé; Jacques Young; Dennis Carson; Marie-Christine Vantyghem; Eva Szarek; Antoine Martinez; Constantine A Stratakis; Jérôme Bertherat; Hervé Lefebvre
Journal:  JCI Insight       Date:  2016-09-22

6.  Case report: Adrenal LH/hCG receptor overexpression and gene amplification causing pregnancy-induced Cushing's syndrome.

Authors:  Michael Herman Chui; Michael Herman Chui; Nese Colak Ozbey; Shereen Ezzat; Yersu Kapran; Yesim Erbil; Sylvia L Asa
Journal:  Endocr Pathol       Date:  2009       Impact factor: 3.943

7.  Improvement of hypercortisolism by β-blocker therapy in subclinical Cushing's syndrome associated with ACTH-independent macronodular adrenocortical hyperplasia.

Authors:  Kenji Oki; Kiminori Yamane; Shuhei Nakanishi; Reiko Nakashima; Kuniaki Jitsuiki; Nobuoki Kohno
Journal:  Endocrine       Date:  2009-10-08       Impact factor: 3.633

8.  Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma.

Authors:  Ulf Elbelt; Alessia Trovato; Michael Kloth; Enno Gentz; Reinhard Finke; Joachim Spranger; David Galas; Susanne Weber; Cristina Wolf; Katharina König; Wiebke Arlt; Reinhard Büttner; Patrick May; Bruno Allolio; Jochen G Schneider
Journal:  J Clin Endocrinol Metab       Date:  2015-01       Impact factor: 5.958

Review 9.  Cell-to-cell communication in bilateral macronodular adrenal hyperplasia causing hypercortisolism.

Authors:  Hervé Lefebvre; Céline Duparc; Gaëtan Prévost; Jérôme Bertherat; Estelle Louiset
Journal:  Front Endocrinol (Lausanne)       Date:  2015-04-20       Impact factor: 5.555

10.  ACTH-independent macronodular adrenocortical hyperplasia reveals prevalent aberrant in vivo and in vitro responses to hormonal stimuli and coupling of arginine-vasopressin type 1a receptor to 11β-hydroxylase.

Authors:  Johannes Hofland; Leo J Hofland; Peter M van Koetsveld; Jacobie Steenbergen; Wouter W de Herder; Casper H van Eijck; Ronald R de Krijger; Francien H van Nederveen; Maarten O van Aken; Johannes W de Groot; Thera P Links; Frank H de Jong; Richard A Feelders
Journal:  Orphanet J Rare Dis       Date:  2013-09-13       Impact factor: 4.123

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