Evidence map›Paper›PMID 35563581›Full record

ArticleInternational journal of molecular sciences2022

Assessment of G Protein-Coupled Oestrogen Receptor Expression in Normal and Neoplastic Human Tissues Using a Novel Rabbit Monoclonal Antibody.

Maria Bubb, Anna-Sophia Lieselott Beyer, Pooja Dasgupta, Daniel Kaemmerer, Jörg Sänger, Katja Evert, Ralph M Wirtz, Stefan Schulz, Amelie Lupp

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Maria BubbInstitute of Pharmacology and Toxicology, Jena University Hospital, 07747 Jena, Germany.
Anna-Sophia Lieselott BeyerInstitute of Pharmacology and Toxicology, Jena University Hospital, 07747 Jena, Germany.
Pooja DasguptaInstitute of Pharmacology and Toxicology, Jena University Hospital, 07747 Jena, Germany.ORCID 0000-0002-6369-122X
Daniel KaemmererDepartment of General and Visceral Surgery, Zentralklinik Bad Berka, 99438 Bad Berka, Germany.
Jörg SängerLaboratory of Pathology and Cytology Bad Berka, 99438 Bad Berka, Germany.
Katja EvertDepartment of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Ralph M WirtzSTRATIFYER Molecular Pathology GmbH, 50935 Cologne, Germany.
Stefan SchulzInstitute of Pharmacology and Toxicology, Jena University Hospital, 07747 Jena, Germany.ORCID 0000-0002-5997-8885
Amelie LuppInstitute of Pharmacology and Toxicology, Jena University Hospital, 07747 Jena, Germany.ORCID 0000-0003-0141-7310
Jena University Hospital · DEZentralklinik Bad Berka · DEUniversitätsmedizin Greifswald · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Antibodies, MonoclonalReceptors, EstrogenAnimalsEstrogensFemaleGTP-Binding ProteinsHumansPregnancyRabbitsReceptors, G-Protein-CoupledAntibodies, MonoclonalEstrogensGTP-Binding ProteinsReceptors, EstrogenReceptors, G-Protein-CoupledantibodyGPERGPR30G-protein-coupled oestrogen receptorimmunohistochemistryneuroendocrinetumours

Identifiers

PMID35563581
PMCPMC9099907
OpenAlexW4229064504

What Socratic holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.