Predicting Response to Medical Treatment in Acromegaly via Granulation Pattern, Expression of Somatostatin Receptors Type 2 and 5 and E-Cadherin

Int J Mol Sci. 2024 Aug 8;25(16):8663. doi: 10.3390/ijms25168663.

Abstract

Resistance to first-generation somatostatin receptor ligand (fgSRL) treatment in acromegaly is common, making the identification of biomarkers that predict fgSRL response a desired goal. We conducted a retrospective analysis on 21 patients with acromegaly who underwent surgery and subsequent pharmacological treatment. Through immunohistochemistry (IHC), we assessed the expression of the somatostatin receptor subtypes SSTR2 and SSTR5, E-Cadherin, and cytokeratin granulation pattern (sparsely or densely). Patients were divided into responders and non-responders based on their biochemical response to fgSRL and/or the newer agent, Pasireotide, or the GH-blocker, Pegvisomant. Patients resistant to fgSRL (n = 12) exhibited lower SSTR2 and E-Cadherin expressions. Sparsely granulated tumors were more frequent in the non-responder group. SSTR2 (p = 0.024, r = 0.49) and E-Cadherin (p = 0.009, r = 0.64) positively correlated with the Insulin-like Growth Factor 1 (IGF-1) decrease after fgSRL, while SSTR5 (p = 0.107, r = -0.37) showed a trend towards negative correlation. SSTR5 positivity seemed to be associated with Pasireotide response, albeit the number of treated patients was too low (n = 4). No IHC markers correlated with Pegvisomant response. Our findings suggest that densely granulated tumors, with positive SSTR2 and E-Cadherin seem to be associated with favorable fgSRL responses. The strongest predictive value of the studied markers was found for E-Cadherin, which seems to surpass even SSTR2.

Keywords: acromegaly; biomarkers; immunohistochemistry; somatostatin receptor ligands; treatment response.

MeSH terms

  • Acromegaly* / drug therapy
  • Acromegaly* / metabolism
  • Adult
  • Aged
  • Cadherins* / metabolism
  • Female
  • Human Growth Hormone / analogs & derivatives
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Middle Aged
  • Receptors, Somatostatin* / metabolism
  • Retrospective Studies
  • Somatostatin / analogs & derivatives
  • Somatostatin / metabolism
  • Somatostatin / therapeutic use
  • Treatment Outcome

Substances

  • Receptors, Somatostatin
  • Cadherins
  • somatostatin receptor 5
  • SSTR2 protein, human
  • Somatostatin
  • Insulin-Like Growth Factor I
  • pegvisomant
  • pasireotide
  • somatostatin receptor 2
  • Human Growth Hormone