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Research Article Free access | 10.1172/JCI118310

Production, characterization, and expression of neuropeptide Y by human pheochromocytoma.

P deS Senanayake, J Denker, E L Bravo, and R M Graham

Department of Molecular Cardiology, Cleveland Clinic Foundation, Ohio 44195, USA.

Find articles by deS Senanayake, P. in: PubMed | Google Scholar

Department of Molecular Cardiology, Cleveland Clinic Foundation, Ohio 44195, USA.

Find articles by Denker, J. in: PubMed | Google Scholar

Department of Molecular Cardiology, Cleveland Clinic Foundation, Ohio 44195, USA.

Find articles by Bravo, E. in: PubMed | Google Scholar

Department of Molecular Cardiology, Cleveland Clinic Foundation, Ohio 44195, USA.

Find articles by Graham, R. in: PubMed | Google Scholar

Published November 1, 1995 - More info

Published in Volume 96, Issue 5 on November 1, 1995
J Clin Invest. 1995;96(5):2503–2509. https://doi.org/10.1172/JCI118310.
© 1995 The American Society for Clinical Investigation
Published November 1, 1995 - Version history
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Abstract

Neuropeptide Y (NPY) levels are increased in plasma and tumors of patients with pheochromocytoma. The present study was designed to evaluate plasma and tissue NPY levels simultaneously as well as to study its release and expression in patients with either adrenal or extraadrenal pheochromocytomas. Plasma NPY levels were higher (P < 0.01) in patients with adrenal tumors than in matched normal subjects and patients with extraadrenal tumors. NPY levels were also higher (P < 0.05) in adrenal than in extraadrenal tumors. Bioactive NPY (1-36) was the predominant form in plasma and tumors of patients with adrenal pheochromocytomas. In contrast, patients with extraadrenal pheochromocytomas had an abundance of NPY fragments. NPY mRNA was abundant in 11 of 13 adrenal tumors but in only 1 of 6 extraadrenal tumors. Moreover, NPY was coreleased with NE with manipulation of adrenal but not extraadrenal tumors. These findings indicate that increased NPY gene expression in adrenal pheochromocytomas accounts for the greater biosynthesis and storage of NPY in these tumors and that increased release of NPY results in elevated plasma NPY. Factors regulating NPY gene expression in pheochromocytoma and the role of NPY in the clinical manifestations of the disease remain to be elucidated.

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