Identification of small-molecule antagonists targeting the growth hormone releasing hormone receptor (GHRHR)
| dc.contributor.author | Matsoukas, Minos-Timotheos | |
| dc.contributor.author | Radomsky, Tarryn | |
| dc.contributor.author | Panagiotopoulos, Vasilis | |
| dc.contributor.author | Preez, Robin du | |
| dc.contributor.author | Papadourakis, Michail | |
| dc.contributor.author | Tsianakas, Konstantinos | |
| dc.contributor.author | Millar, Robert P. | |
| dc.contributor.author | Anderson, Ross C. | |
| dc.contributor.author | Spyroulias, Georgios C. | |
| dc.contributor.author | Newton, Claire L. | |
| dc.date.accessioned | 2026-03-18T23:47:10Z | |
| dc.date.available | 2026-03-18T23:47:10Z | |
| dc.date.issued | 2024-09-23 | |
| dc.description.abstract | The growth hormone-releasing hormone receptor (GHRHR) belongs to Class B1 of G protein-coupled receptors (GPCRs). Class B1 GPCR peptides such, as growth hormone-releasing hormone (GHRH), have been proposed to bind in a two-step model, where first the C-terminal region of the peptide interacts with the extracellular domain of the receptor and, subsequently, the N-terminus interacts with the seven transmembrane domain of the receptor, resulting in activation. The GHRHR has recently been highlighted as a promising drug target toward several types of cancer and has been shown to be overexpressed in prostate, breast, pancreatic, and ovarian cancer. Indeed, peptide GHRHR antagonists have displayed promising results in many cancer models. However, no nonpeptide GHRHR-targeting compounds have yet been identified. We have utilized several computational tools to target GHRHR and identify potential small-molecule compounds directed at this receptor. These compounds were validated using a cyclic adenosine monophosphate (cAMP) ELISA to measure activity at the GHRHR. results suggest that several of the novel small-molecule compounds could inhibit GHRH-induced cAMP accumulation. Preliminary analysis of the specificity/selectivity of one of the most effective hit compounds indicated that the effect seen was via inhibition of the GHRHR. We therefore report the first nonpeptide antagonists of GHRHR and propose a structural basis for inhibition induced by the compounds, which may assist in the future design of lead GHRHR compounds for treating disorders attributed to dysregulated/aberrant GHRHR signaling. | |
| dc.identifier.other | 39207455 | |
| dc.identifier.uri | https://hdl.handle.net/10889/31714 | |
| dc.language.iso | en | |
| dc.publisher | ACS | |
| dc.subject | Antagonists | |
| dc.subject | Ligands | |
| dc.subject | Peptides and proteins | |
| dc.subject | Pharmacophores | |
| dc.subject | Receptors | |
| dc.title | Identification of small-molecule antagonists targeting the growth hormone releasing hormone receptor (GHRHR) | |
| dc.type | Article | |
| oaire.fundingReference.funderName | European Union - 101087215 ERA Chair Life Sciences Program to EmpoweR moleculAr aNd struCtural biology initiativEs at UPAT | |
| oaire.resourceType | bibliography | |
| oaire.version | http://purl.org/coar/version/c_970fb48d4fbd8a85 |