Reference : The novel somatostatin analog SOM230 is a potent inhibitor of hormone release by grow...
Scientific journals : Article
Human health sciences : Endocrinology, metabolism & nutrition
http://hdl.handle.net/2268/23746
The novel somatostatin analog SOM230 is a potent inhibitor of hormone release by growth hormone- and prolactin-secreting pituitary adenomas in vitro.
English
Hofland, Leo J [> > > >]
van der Hoek, Joost [> > > >]
van Koetsveld, Peter M [> > > >]
de Herder, Wouter W [> > > >]
Waaijers, Marlijn [> > > >]
Sprij-Mooij, Diana [> > > >]
Bruns, Christian [> > > >]
Weckbecker, Gisbert [> > > >]
Feelders, Richard [> > > >]
van der Lely, Aart-Jan [> > > >]
Beckers, Albert mailto [Université de Liège - ULiège > Département des sciences cliniques > Endocrinologie >]
Lamberts, Steven WJ [> > > >]
Apr-2004
Journal of Clinical Endocrinology and Metabolism
Endocrine Society
89
4
1577-1585
Yes (verified by ORBi)
International
0021-972X
Chevy Chase
MD
[en] Adenoma/secretion ; Adult ; Dose-Response Relationship, Drug ; Female ; Hormone Antagonists/administration & dosage/pharmacology ; Human Growth Hormone/antagonists & inhibitors/secretion ; Humans ; Male ; Middle Aged ; Octreotide/administration & dosage/pharmacology ; Pituitary Neoplasms/secretion ; Prolactin/antagonists & inhibitors/secretion ; Protein Isoforms/genetics ; RNA, Messenger/metabolism ; Receptors, Somatostatin/genetics ; Somatostatin/administration & dosage/analogs & derivatives/pharmacology ; Tumor Cells, Cultured
[en] To determine the inhibitory profile of the novel somatostatin (SRIF) analog SOM230 with broad SRIF receptor binding, we compared the in vitro effects of SOM230, octreotide (OCT), and SRIF-14 on hormone release by cultures of different types of secreting pituitary adenomas. OCT (10 nM) significantly inhibited GH release in seven of nine GH-secreting pituitary adenoma cultures (range, -26 to -73%), SOM230 (10 nM) in eight of nine cultures (range, -22 to -68%), and SRIF-14 (10 nM) in six of six cultures (range, -30 to -75%). The sst analysis showed predominant but variable levels of somatostatin receptor (sst)(2) and sst(5) mRNA expression. In one culture completely resistant to OCT, SOM230 and SRIF-14 significantly inhibited GH release in a dose-dependent manner with an IC(50) value in the low nanomolar range. In the other cultures, SOM230 showed a lower potency of GH release inhibition (IC(50), 0.5 nM), compared with OCT (IC(50), 0.02 nM) and SRIF-14 (IC(50), 0.02 nM). A positive correlation was found between sst(2) but not sst(5) mRNA levels in the adenoma cells and the inhibitory potency of OCT on GH release in vivo and in vitro, and the effects of SOM230 and SRIF-14 in vitro. In three prolactinoma cultures, 10 nM OCT weakly inhibited prolactin (PRL) release in only one (-28%), whereas 10 nM SOM230 significantly inhibited PRL release in three of three cultures (-23, -51, and -64.0%). The inhibition of PRL release by SOM230 was related to the expression level of sst(5) but not sst(2) mRNA. Several conclusions were reached. First, SOM230 has a broad profile of inhibition of tumoral pituitary hormone release in the low nanomolar range, probably mediated via both sst(2) and sst(5) receptors. The higher number of responders of GH-secreting pituitary adenoma cultures to SOM230, compared with OCT, suggest that SOM230 has the potency to increase the number of acromegalic patients which can be biochemically controlled. Second, compared with OCT, SOM230 is more potent in inhibiting PRL release by mixed GH/PRL-secreting adenoma and prolactinoma cells.
Researchers ; Professionals
http://hdl.handle.net/2268/23746
10.1210/jc.2003-031344

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