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A Potential Inhibitory Role for the New Truncated Variant of Somatostatin Receptor 5, sst5TMD4, in Pituitary Adenomas Poorly Responsive to Somatostatin Analogs
Author(s) -
Mario DuránPrado,
Alexandru Saveanu,
Raúl M. Luque,
Manuel D. Gahete,
Francisco GraciaNavarro,
P Jaquet,
Henry Dufour,
Marı́a M. Malagón,
Michael D. Culler,
Anne Barlier,
Justo P. Castaño
Publication year - 2010
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/jc.2009-2247
Subject(s) - somatostatin , somatostatin receptor , in vivo , octreotide , somatostatin receptor 2 , medicine , endocrinology , agonist , receptor , in vitro , context (archaeology) , biology , hormone , pituitary tumors , biochemistry , paleontology , microbiology and biotechnology
Somatostatin (SST) receptors, specially sst2 and sst5, provide a valuable target to inhibit excessive hormone release and cell growth in pituitary tumors by using SST analogs (SSAs). Unfortunately, an appreciable proportion of tumors fail to respond to SSA despite expressing high levels of one or more ssts. Recently we identified two novel truncated sst5 variants, sst5TMD5, and sst5TMD4, absent in normal pituitary but expressed in pituitary tumors.

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