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

Endocrinol Nutr. 2014 Dec;61(10):523-30. doi: 10.1016/j.endonu.2014.05.006. Epub 2014 Jul 5.
[Article in English, Spanish]

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.

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

MeSH terms

  • Acromegaly / etiology
  • Adenoma / chemistry*
  • Adenoma / complications
  • Adenoma / drug therapy
  • Adenoma / surgery
  • Antineoplastic Agents, Hormonal / therapeutic use
  • Combined Modality Therapy
  • Drug Resistance, Neoplasm
  • Gene Expression Regulation, Neoplastic
  • Growth Hormone-Secreting Pituitary Adenoma / chemistry*
  • Growth Hormone-Secreting Pituitary Adenoma / complications
  • Growth Hormone-Secreting Pituitary Adenoma / drug therapy
  • Growth Hormone-Secreting Pituitary Adenoma / surgery
  • Human Growth Hormone / analysis
  • Human Growth Hormone / metabolism*
  • Humans
  • Hypophysectomy
  • Insulin-Like Growth Factor I / analysis
  • Neoplasm Proteins / biosynthesis*
  • Neoplasm Proteins / genetics
  • Octreotide / therapeutic use*
  • Real-Time Polymerase Chain Reaction
  • Receptors, Somatostatin / biosynthesis*
  • Receptors, Somatostatin / genetics
  • Tissue Array Analysis

Substances

  • Antineoplastic Agents, Hormonal
  • Neoplasm Proteins
  • Receptors, Somatostatin
  • SSTR2 protein, human
  • Human Growth Hormone
  • Insulin-Like Growth Factor I
  • somatostatin receptor 5
  • Octreotide