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Selective Activation of Somatostatin Receptor Subtypes Differentially Modulates Secretion and Viability in Human Medullary Thyroid Carcinoma Primary Cultures: Potential Clinical Perspectives
Author(s) -
Maria Chiara Zatelli,
Daniela Piccin,
Federico Tagliati,
Arianna Bottoni,
Andrea Luchin,
Cristina Vignali,
Angelo Margutti,
Marta Bondanelli,
Gian Carlo Pansini,
Maria Rosa Pelizzo,
Michael D. Culler,
Ettore C. degli Uberti
Publication year - 2006
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2006-0334
Subject(s) - somatostatin receptor 2 , somatostatin receptor , somatostatin , endocrinology , medicine , somatostatin receptor 1 , agonist , lanreotide , chromogranin a , biology , receptor , cancer research , acromegaly , hormone , immunohistochemistry , growth hormone
Medullary thyroid carcinoma (MTC) is a rare tumor originating from thyroid parafollicular C cells. We previously demonstrated that somatostatin (SRIH) reduces cell growth in the human MTC cell line, TT, which expresses all SRIH receptor (SSTR) subtypes and responds differently to selective SSTR agonists.

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