H. Lefebvre et al., CHARACTERIZATION OF THE SOMATOSTATIN RECEPTOR SUBTYPE IN A BRONCHIAL CARCINOID-TUMOR RESPONSIBLE FOR CUSHINGS-SYNDROME, The Journal of clinical endocrinology and metabolism, 80(4), 1995, pp. 1423-1428
Small ACTH-secreting carcinoid tumors responsible for Cushing's syndro
me are often difficult to localize using available radiological invest
igations. Somatostatin receptors have been found in about 90% of carci
noid tumors studied, leading to a new approach for the localization of
tumors or metastasis by using radiolabeled somatostatin analogs. We r
eport a case of Cushing's syndrome due to an ACTH-secreting bronchial
carcinoid tumor, completely suppressible with octreotide treatment and
evidenced by body scintigraphy with In-111-labeled pentreotide. After
removal, which led to patient recovery, the tumor was studied in vitr
o. In situ hybridization, using a complementary DNA probe, revealed PO
MC messenger ribonucleic acid in a subpopulation of tumor cells. These
cells were labeled by immunochemistry using an antiserum directed aga
inst ACTH. Confocal laser scanning microscopy analysis showed that the
ACTH-immunoreactive peptide was sequestered in secretory granules. Au
toradiographic labeling using [I-125-Tyr(0),D-Trp(8)]somatostatin-14 d
emonstrated the presence of somatostatin-binding sites in the whole tu
mor tissue. The relative affinities of various selective somatostatin
analogs and the ability of GTP to inhibit radioligand binding suggeste
d that the receptor expressed in the tumor cells belonged to the SSTR-
2 subtype.