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Accepted Preprint first posted online on 29 October 2008

Journal of Endocrinology 2009;200:167.

Journal of Endocrinology (2008) In press
DOI: 10.1677/JOE-08-0395
© 2008 Society for Endocrinology
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RESEARCH

Expression Profiles of the Glucose-Dependent Insulinotropic Peptide Receptor and Luteinizing Hormone Receptor in Sporadic Adrenocortical Tumors

Marcia Helena Soares Costa, Ana Claudia Latronico, Regina Matsunaga Martin, Angela S Barbosa, Madson Q Almeida, Claudimara Ferini Pacicco Lotfi, Helena P Lima Valassi, Mirian Yumie Nishi, Antonio Marmo Lucon, Sheila Aparecida Siqueira, Maria Claudia Nogueira Zerbini, Luciani Renata Carvalho, Berenice Bilharinho Mendonca and Maria Candida Barisson Villares Fragoso

M Costa, Endocrinology, Hospital das Clinicas, Sao Paulo, Brazil
A Latronico, Hospital das Clinicas, Endocrinology, SP, Brazil
R Martin, Hospital das Clinicas, Endocrinology, SP, Brazil
A Barbosa, SP, Brazil
M Almeida, Hospital das Clinicas, Endocrinology, SP, Brazil
C Lotfi, Anatomia, Laboratorio de Estrutura e Funcao Celular, SP, Brazil
H Valassi, SP, Brazil
M Nishi, SP, Brazil
A Lucon, Urology, Hospital das Clinicas, SP, Brazil
S Siqueira, Pathology, Hospital das Clinicas, Sao Paulo, Brazil
M Zerbini, SP, Brazil
L Carvalho, SP, Brazil
B Mendonca, Hospital das Clinicas, Endocrinology, SP, Brazil
M Fragoso, SP, Brazil

Correspondence: Marcia Helena Soares Costa, Email: mhsc{at}usp.br

Abstract

Glucose-dependent insulinotropic peptide receptor (GIPR) and luteinizing hormone receptor (LHCGR) are G-protein coupled receptors with a wide tissue expression pattern. Aberrant expression of these receptors has been rarely demonstrated in adult sporadic adrenocortical tumors with a lack of data on pediatric tumors. We quantified the GIPR and LHCGR expression in a large cohort of fifty five patients (25 children and 30 adults) with functioning and non-functioning sporadic adrenocortical tumors. Thirty eight tumors were classified as adenomas whereas 17 were carcinomas.

GIPR and LHCGR expression was analyzed by real time PCR and normal human pancreatic and testicular tissue samples were used as positive controls, respectively. Mean expression values were determined by fold increase in comparison to a normal adrenal pool. GIPR mRNA levels were significantly higher in adrenocortical carcinomas than in adenomas from both pediatric and adult groups. LHCGR expression was similar in both carcinomas and adenomas from the pediatric group but significantly lower in carcinomas than in adenomas from the adult group (median 0.06 and 2.3, respectively, p<0.001). GIPR was detected by immunohistochemistry in both pediatric and adult tumors. Staining and real time PCR results correlated positively only when GIPR mRNA levels were at least 2-fold increased in comparison to normal adrenal expression levels.

In conclusion, GIPR overexpression was observed in pediatric and adult adrenocortical tumors and very low levels of LHCGR expression were found in all adult adrenocortical carcinomas.







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