Literature DB >> 25008035

Cytoplasmic expression of SSTR2 and 5 by immunohistochemistry and by RT/PCR is not associated with the pharmacological response to octreotide.

Baldomero Gonzalez1, Guadalupe Vargas1, Claudia Ramirez1, Silvia Asa2, Sonia Cheng2, Carolina Sandoval1, Moises Mercado3.   

Abstract

OBJECTIVE: To evaluate expression of somatostatin receptor subtypes 2 and 5 (SSTR 2 and 5) by RT/PCR and immunohistochemistry (IHC) in GH-secreting adenomas, seeking correlations with response to octreotide.
METHODS: SSTR2 and 5 expression was tested by IHC (n=37), RT/PCR (n=36) or both (n=13) in GH-secreting adenomas from 60 patients with acromegaly who had undergone pituitary surgery; 36 had been treated preoperatively with octreotide LAR for 3-6 months, and were categorized as responders (achievement of GH <2.5ng/mL and a normal age-adjusted IGF-1), partial responders (GH and IGF-1 reduction >50% and >30%, respectively) or non-responders. IHC was performed on a tissue microarray using specific antibodies directed to the carboxyl terminus of SSTR2 and 5.
RESULTS: SSTR5 was the predominantly expressed receptor subtype by both IHC and RT/PCR in all tumors tested, regardless of whether they came from octreotide-naïve, octreotide-responsive, or octreotide-resistant patients. Immunostaining was concentrated in the cytoplasm. Neither SSTR2 nor SSTR5 expression correlated with baseline or post-octreotide GH or IGF-1 levels or tumor volume by either method. The agreement rate between RT/PCR and IHC was 77% in all 13 adenomas in which both methods were used.
CONCLUSION: Expression of these receptors does not guarantee an adequate response to somatostatin analogs; other functional aspects of this interaction, such as receptor homo- and heterodimerization, and the resulting signaling cascade, probably play a role in determining whether a patient will respond or not to these agents.
Copyright © 2014 SEEN. Published by Elsevier Espana. All rights reserved.

Entities:  

Keywords:  Acromegalia; Acromegaly; Análogos de la somatostatina; Octreotide; Octreótido; Receptores somatostatinérgicos; Somatostatin analogs; Somatostatin receptors

Mesh:

Substances:

Year:  2014        PMID: 25008035     DOI: 10.1016/j.endonu.2014.05.006

Source DB:  PubMed          Journal:  Endocrinol Nutr        ISSN: 1575-0922


  4 in total

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