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Growth Hormone Secretagogue Receptor Expression in Human Pituitary Tumors1
Author(s) -
Monica M. Skinner,
Ralf Nass,
Beatriz Lopes,
Edward R. Laws,
Michael O. Thorner
Publication year - 1998
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jcem.83.12.5307
Subject(s) - endocrinology , medicine , secretagogue , receptor , adenoma , messenger rna , pituitary adenoma , pituitary tumors , prolactin , pituitary neoplasm , pituitary gland , anterior pituitary , somatotropic cell , biology , chemistry , hormone , gene , biochemistry
The GH secretagogue (GHS) receptor (GHS-R) has been characterized and cloned. It is a member of a family of seven transmembrane receptors and is closely related to the neurotensin and TRH receptors. To determine the expression of this receptor in normal anterior pituitary and in 24 human pituitary adenomas, we analyzed GHS-R messenger ribonucleic acid (mRNA) using a RT-PCR assay. We found that normal human pituitary was positive for the GHS-R signal. In addition, all GH-secreting adenomas and the one TSH-secreting adenoma demonstrated the presence of GHS-R mRNA. Three of four ACTH-secreting tumors and three of nine gonadotroph adenomas were also positive for the GHS-R mRNA. To determine the amounts of GHS-R mRNA in normal pituitary and in representative tumors, semiquantitative competitive PCR was performed. We determined that normal pituitary had approximately 750 molecules/L GHS-R mRNA. The acromegalic tumor had approximately 1.5 × 105 molecules/L, and the TSH-secreting tumor had approximately 7.5 × 103 molecules/L. Other tumor types contained considerably less, with the ACTH-secreting and gonadotroph tumors expressing 7.5 × 102 and 3 × 102 GHS-R mRNA molecules/L, respectively. These results suggest that GH- and TSH-producing adenomas express GHS-R mRNA at levels 200 and 10 times higher, respectively, than the normal pituitary, and that this receptor expression may be involved in the pathogenesis and growth of these pituitary adenomas.

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