2004
DOI: 10.4161/cbt.3.8.1030
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Somatostatin and cancer: Applying endocrinology to oncology

Abstract: Somatostatin is a peptide hormone that normally suppresses growth hormone (GH), thyrotropin (TSH), insulin and gut hormone release, as well as affecting multiple aspects of gastrointestinal function. It achieves these pleiotropic effects by binding somatostatin receptors (SSTR), a family of five G-protein coupled membrane receptors. Somatostatin analogs, such as octreotide, lanreotide and vapreotide, are well-established treatments for tumors that over secrete these hormones. Recently, use of somatostatin anal… Show more

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Cited by 22 publications
(16 citation statements)
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“…56 Somatostatin is a peptide hormone that normally suppresses growth hormone (GH), thyrotropin (TSH), insulin, and gut hormone release, as well as affecting gastrointestinal function. 57 It achieves these pleiotropic effects by binding somatostatin receptors (SSTR), a family of five G-protein-coupled membrane receptors. In thymomas with a high uptake of octreotide on scintigraphy, SST analogs are a therapeutic option even for advanced chemorefractory patients not considered eligible for additional conventional chemotherapy or debulking surgery.…”
Section: Clinical Implications and Novel Therapeutic Perspectivesmentioning
confidence: 99%
“…56 Somatostatin is a peptide hormone that normally suppresses growth hormone (GH), thyrotropin (TSH), insulin, and gut hormone release, as well as affecting gastrointestinal function. 57 It achieves these pleiotropic effects by binding somatostatin receptors (SSTR), a family of five G-protein-coupled membrane receptors. In thymomas with a high uptake of octreotide on scintigraphy, SST analogs are a therapeutic option even for advanced chemorefractory patients not considered eligible for additional conventional chemotherapy or debulking surgery.…”
Section: Clinical Implications and Novel Therapeutic Perspectivesmentioning
confidence: 99%
“…Another way that brain insulin can influence the functions of the thyroid system is through the somatostatin signaling system. Somatostatin is one of the most important regulators of the HPT axis, due to its suppression of TRH and TSH secretion [44,45]. There is evidence that in DM1 somatostatin level can be increased, as shown in human DM1 and in the gastrointestinal tract of nonobese diabetic mice [46][47][48], or can be unchanged or reduced, as demonstrated in rats with STZ-induced DM [49][50][51].…”
Section: Endocrine Researchmentioning
confidence: 99%
“…A long lasting experience has been accumulated with the employment of SS analogs for diagnostic and therapeutic purposes, as opposed to CST analogs, which are currently under investigation. A recent commentary (Grimberg 2004) SS analogs were synthesized on the basis of structural and functional data on SS-14, showing that aminoacidic residues in positions 7-10 were fundamental for its biological activity (Raynor et al 1993b). Among the numerous designed hexa-and octa-peptides, the latter, for example octreotide and lanreotide, have a high affinity for sst types 2, 3 and 5 and are registered in most countries for clinical use (deHerder & Lamberts 2002).…”
Section: Effects On Tumour Cell Growthmentioning
confidence: 99%