Evidence map›Paper›PMID 35236104›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2022

A Thromboxane A

Robert Eckenstaler, Anne Ripperger, Michael Hauke, Markus Petermann, Sandra A Hemkemeyer, Edzard Schwedhelm, Süleyman Ergün, Maike Frye, Oliver Werz, Andreas Koeberle and 2 more

Abstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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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

12 authors.

Robert Eckenstaler *Department of Clinical Pharmacy and Pharmacotherapy, Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Germany (R.E., A.R., M.H., M.P., H.B., R.A.B.).ORCID 0000-0002-2810-5045
Anne Ripperger *Department of Clinical Pharmacy and Pharmacotherapy, Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Germany (R.E., A.R., M.H., M.P., H.B., R.A.B.).
Michael HaukeDepartment of Clinical Pharmacy and Pharmacotherapy, Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Germany (R.E., A.R., M.H., M.P., H.B., R.A.B.).
Markus PetermannDepartment of Clinical Pharmacy and Pharmacotherapy, Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Germany (R.E., A.R., M.H., M.P., H.B., R.A.B.).ORCID 0000-0002-7373-7332
Sandra A HemkemeyerInstitute of Clinical Chemistry and Laboratory Medicine (S.A.H., M.F.), University Medical Center Hamburg-Eppendorf, Germany.ORCID 0000-0003-1854-9512
Edzard SchwedhelmInstitute of Clinical Pharmacology and Toxicology (E.S.), University Medical Center Hamburg-Eppendorf, Germany.ORCID 0000-0003-3597-6276
Süleyman ErgünInstitute of Anatomy and Cell Biology, Julius-Maximilians-University Würzburg, Germany (S.E.).
Maike FryeInstitute of Clinical Chemistry and Laboratory Medicine (S.A.H., M.F.), University Medical Center Hamburg-Eppendorf, Germany.ORCID 0000-0002-6257-7636
Oliver WerzDepartment of Pharmaceutical/Medicinal Chemistry, Institute of Pharmacy, Friedrich-Schiller-University Jena, Germany (O.W., A.K.).ORCID 0000-0002-5064-4379
Andreas KoeberleDepartment of Pharmaceutical/Medicinal Chemistry, Institute of Pharmacy, Friedrich-Schiller-University Jena, Germany (O.W., A.K.).ORCID 0000-0001-6269-5088
Heike BraunDepartment of Clinical Pharmacy and Pharmacotherapy, Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Germany (R.E., A.R., M.H., M.P., H.B., R.A.B.).
Ralf A BenndorfDepartment of Clinical Pharmacy and Pharmacotherapy, Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Germany (R.E., A.R., M.H., M.P., H.B., R.A.B.).ORCID 0000-0001-6493-4521

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTP (thromboxane A

methodsWe combined global transcriptome analysis, lipid mediator profiling, functional cell analyses, and in vivo angiogenesis assays to study the effects of endothelial TP overexpression or knockdown/knockout on the angiogenic capacity of endothelial cells in vitro and in vivo.

resultsHere we report that endothelial TP expression induces COX-2 (cyclooxygenase-2) in a G

conclusionsOur work uncovers a TP-driven COX-2-dependent feedback loop and important effector mechanisms that directly link TP upregulation to angiostatic TP signaling in endothelial cells. By these previously unrecognized mechanisms, pathological endothelial upregulation of the TP could directly foster endothelial dysfunction, microvascular rarefaction, and systemic hypertension even in the absence of exogenous sources of TP agonists.

Indexed as

Endothelial CellsReceptors, ThromboxaneCyclooxygenase 2FeedbackHomeostasisHumansReceptors, Thromboxane A2, Prostaglandin H2Thromboxane A2ThromboxanesCyclooxygenase 2Receptors, ThromboxaneReceptors, Thromboxane A2, Prostaglandin H2Thromboxane A2Thromboxanesangiogenesiscyclooxygenase 2endothelial cellsendothelial dysfunctionprostaglandin H2thromboxan A2 receptor

Identifiers

PMID35236104
PMCPMC8939709

What OpenQuestion 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 OpenQuestion graph.