Assessment of G Protein-Coupled Oestrogen Receptor Expression in Normal and Neoplastic Human Tissues Using a Novel Rabbit Monoclonal Antibody.
Maria BubbAnna-Sophia Lieselott BeyerPooja DasguptaDaniel KaemmererJörg SängerKatja EvertRalph M WirtzStefan SchulzAmelie LuppPublished in: International journal of molecular sciences (2022)
In addition to the classical oestrogen receptors, ERα and ERβ, a G protein-coupled oestrogen receptor (GPER) has been identified that primarily mediates the rapid, non-genomic signalling of oestrogens. Data on GPER expression at the protein level are contradictory; therefore, the present study was conducted to re-evaluate GPER expression by immunohistochemistry to obtain broad GPER expression profiles in human non-neoplastic and neoplastic tissues, especially those not investigated in this respect so far. We developed and thoroughly characterised a novel rabbit monoclonal anti-human GPER antibody, 20H15L21, using Western blot analyses and immunocytochemistry. The antibody was then applied to a large series of formalin-fixed, paraffin-embedded human tissue samples. In normal tissue, GPER was identified in distinct cell populations of the cortex and the anterior pituitary; islets and pancreatic ducts; fundic glands of the stomach; the epithelium of the duodenum and gallbladder; hepatocytes; proximal tubules of the kidney; the adrenal medulla; and syncytiotrophoblasts and decidua cells of the placenta. GPER was also expressed in hepatocellular, pancreatic, renal, and endometrial cancers, pancreatic neuroendocrine tumours, and pheochromocytomas. The novel antibody 20H15L21 will serve as a valuable tool for basic research and the identification of GPER-expressing tumours during histopathological examinations.
Keyphrases
- estrogen receptor
- endothelial cells
- induced pluripotent stem cells
- poor prognosis
- pluripotent stem cells
- gene expression
- stem cells
- induced apoptosis
- oxidative stress
- mesenchymal stem cells
- functional connectivity
- electronic health record
- mass spectrometry
- bone marrow
- quantum dots
- protein protein
- dna methylation
- signaling pathway
- cell proliferation
- genome wide
- artificial intelligence
- atomic force microscopy
- loop mediated isothermal amplification