2008
DOI: 10.1016/j.mce.2007.10.015
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Somatostatin and somatostatin receptors in Cushing's disease

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Cited by 52 publications
(24 citation statements)
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“…The GPCRs superfamily of receptors, which includes the sst1-5 family, is associated with a number of important physio-pathological functions [41][42][43]. This explains the increasing interest in this research area, which is also supported by the fact that roughly 30% of marketed drugs target GPCRs, as is the case for synthetic SST analogs used to control cell growth and hormonal hypersecretion in pituitary adenomas and other neuroendocrine tumors [44,45].…”
Section: Discussionmentioning
confidence: 99%
“…The GPCRs superfamily of receptors, which includes the sst1-5 family, is associated with a number of important physio-pathological functions [41][42][43]. This explains the increasing interest in this research area, which is also supported by the fact that roughly 30% of marketed drugs target GPCRs, as is the case for synthetic SST analogs used to control cell growth and hormonal hypersecretion in pituitary adenomas and other neuroendocrine tumors [44,45].…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, sst 2 overexpression prevented octreotide desensitization in these cells (34). Thus, it may be an interesting concept to treat CD patients with cortisol-lowering therapy, which, in case of reappearing sst 2 protein expression, is followed by treatment with an sst 2 -preferring somatostatin analog (35,36). In support of this hypothesis, the primary culture in which octreotide showed the largest ACTH-lowering effect was the one in which sst 2 protein expression was highest, with an immunoreactivity score of 6.…”
Section: Figurementioning
confidence: 99%
“…Various somatostatin receptor agonists have demonstrated inhibitory effects on tumor cell proliferation in pituitary tumors, including somatotroph and thyrotroph tumors. In some patients with Cushing's disease, SOM230 has shown promising effects by decreasing the levels of plasma ACTH and urinary free cortisol [6,7]. Novel somatostatin-dopamine chimeric molecules or retinoic acid also appear to be a promising approach [8,9].…”
Section: Introductionmentioning
confidence: 99%