Evidence map›Paper›PMID 34884783›Full record

ArticleInternational journal of molecular sciences2021

Reassessment of SST4 Somatostatin Receptor Expression Using SST4-eGFP Knockin Mice and the Novel Rabbit Monoclonal Anti-Human SST4 Antibody 7H49L61.

Amelie Lupp, Blanca Ehms, Ralf Stumm, Johannes Göckeritz, Christian Mawrin, Stefan Schulz

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Glioma and Peptidergic Systems: Oncogenic and Anticancer Peptides.International journal of molecular sciences · 2024
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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

6 authors at 2 institutions in 1 country.

Amelie LuppInstitute of Pharmacology and Toxicology, Jena University Hospital, D-07747 Jena, Germany.ORCID 0000-0003-0141-7310
Blanca EhmsInstitute of Pharmacology and Toxicology, Jena University Hospital, D-07747 Jena, Germany.
Ralf StummInstitute of Pharmacology and Toxicology, Jena University Hospital, D-07747 Jena, Germany.
Johannes GöckeritzInstitute of Pharmacology and Toxicology, Jena University Hospital, D-07747 Jena, Germany.
Christian MawrinInstitute of Neuropathology, University Hospital, Otto-von-Guericke-University, 39120 Magdeburg, Germany.
Stefan SchulzInstitute of Pharmacology and Toxicology, Jena University Hospital, D-07747 Jena, Germany.ORCID 0000-0002-5997-8885
Jena University Hospital · DEOtto-von-Guericke-Universität Magdeburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among the five somatostatin receptors (SST1-SST5), SST4 is the least characterized, which is in part due to the lack of specific monoclonal antibodies. We generated a knockin mouse model that expresses a carboxyl-terminal SST4-eGFP fusion protein. In addition, we extensively characterized the novel rabbit monoclonal anti-human SST4 antibody 7H49L61 using transfected cells and receptor-expressing tissues. 7H49L61 was then subjected to immunohistochemical staining of a series of formalin-fixed, paraffin-embedded normal and neoplastic human tissues. Characterization of SST4-eGFP mice revealed prominent SST4 expression in cortical pyramidal cells and trigeminal ganglion cells. In the human cortex, 7H49L61 disclosed a virtually identical staining pattern. Specificity of 7H49L61 was demonstrated by detection of a broad band migrating at 50-60 kDa in immunoblots. Tissue immunostaining was abolished by preadsorption of 7H49L61 with its immunizing peptide. In the subsequent immunohistochemical study, 7H49L61 yielded a predominant plasma membrane staining in adrenal cortex, exocrine pancreas, and placenta. SST4 was also found in glioblastomas, parathyroid adenomas, gastric and pancreatic adenocarcinomas, pheochromocytomas, and lymphomas. Altogether, we provide the first unequivocal localization of SST4 in normal and neoplastic human tissues. The monoclonal antibody 7H49L61 may also prove of great value for identifying SST4-expressing tumors during routine histopathological examinations.

Indexed as

Gene Knock-In TechniquesAnimalsAntibodies, MonoclonalCell LineGreen Fluorescent ProteinsHEK293 CellsHumansImmunohistochemistryMiceMice, Inbred C57BLModels, AnimalNeoplasmsReceptors, SomatostatinRecombinant Fusion ProteinsStaining and LabelingAntibodies, MonoclonalGreen Fluorescent ProteinsReceptors, SomatostatinRecombinant Fusion Proteinssomatostatin receptor subtype-4antibodyimmunohistochemistrysomatostatinsomatostatin receptorSST4tumors

Identifiers

PMID34884783
PMCPMC8657703
OpenAlexW3215699229

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.