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Journal of Clinical Endocrinology & Metabolism , doi:10.1210/jc.2006-0728
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Right arrow Neuroendocrinology and Pituitary
The Journal of Clinical Endocrinology & Metabolism Vol. 92, No. 1 65-69
Copyright © 2007 by The Endocrine Society

Dopamine Receptor Expression and Function in Corticotroph Ectopic Tumors

Rosario Pivonello, Diego Ferone, Wouter W. de Herder, Antongiulio Faggiano, Lisa Bodei, Ronald R. de Krijger, Gaetano Lombardi, Annamaria Colao, Steven W. J. Lamberts and Leo J. Hofland

Departments of Internal Medicine (R.P., D.F., W.W.d.H., S.W.J.L., L.J.H.) and Pathology (R.R.d.K.), Erasmus Medical Center, 3015 GE Rotterdam, The Netherlands; Departments of Molecular and Clinical Endocrinology and Oncology (R.P., A.F., G.L., A.C.), "Federico II" University of Naples, 80131 Naples, Italy; Department of Nuclear Medicine, European Institute of Oncology (L.B.), 20141 Milan, Italy; and Department of Endocrinological and Metabolic Sciences and Center of Excellence for Biomedical Research (D.F.), University of Genoa, 16132 Genoa, Italy

Address all correspondence and requests for reprints to: Rosario Pivonello, M.D., Ph.D., Department of Molecular and Clinical Endocrinology and Oncology, "Federico II" University, Via Sergio Pansini, 5, 80131 Naples, Italy. E-mail: rpivone{at}tin.it.

Background: Dopamine receptor (DR) expression and dopamine agonist (DA) effectiveness have never been demonstrated in neuroendocrine tumors associated with ectopic ACTH syndrome (EAS).

Aim: The aim of the current study was to evaluate DR and particularly D2 subtype expression in neuroendocrine tumors associated with EAS and to evaluate the in vivo effectiveness of the DA cabergoline in the treatment of EAS.

Patients and Methods: Six ACTH-secreting neuroendocrine tumors, including four lung, one pancreatic, and one thymic carcinoid, were used for the evaluation of D2 expression by immunohistochemistry. DR subtypes and D2 isoforms and number were evaluated by RT-PCR in three cases of persistent EAS after surgery. These patients were treated with cabergoline at the dose of 3.5 mg/wk for 6 months. Clinical parameters, hormonal levels, and tumor size were monitored during the treatment period.

Results: At immunohistochemistry, D2 was expressed in five (83.3%) tumors. At RT-PCR, D2 was confirmed in all three cases but at variable numbers, whereas D4 was expressed in two cases. D2long was expressed in all three cases, together with D2short in one case. A normalization of urinary cortisol levels was found in two patients (66.7%) after 3 months of treatment. However, treatment escape was demonstrated in one of these patients afterward.

Conclusion: The results of this study demonstrated that DR are expressed in neuroendocrine tumors associated with EAS and that cabergoline treatment could be effective in controlling cortisol excess in a subgroup of patients with EAS. Further studies on a larger number of patients are mandatory to confirm the usefulness of DA in EAS.




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