Evidence map›Paper›PMID 30038709›Full record

ArticleOncotarget2018

TRPC4/TRPC5 channels mediate adverse reaction to the cancer cell cytotoxic agent (-)-Englerin A.

Sin Ying Cheung, Matthias Henrot, Mohammad Al-Saad, Matthias Baumann, Heiko Muller, Anke Unger, Hussein N Rubaiy, Ilka Mathar, Klaus Dinkel, Peter Nussbaumer and 10 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

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  13. How TRPC Channels Modulate Hippocampal Function.International journal of molecular sciences · 2020
    Review
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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

20 authors at 5 institutions in 2 countries.

Sin Ying CheungSchool of Medicine, University of Leeds, Leeds, LS2 9JT, England, UK.
Matthias HenrotInstitute of Chemistry and Biochemistry, Freie Universität Berlin, 14195 Berlin, Germany.
Mohammad Al-SaadSchool of Biomedical Sciences, University of Leeds, Leeds, LS2 9JT, UK.
Matthias BaumannLead Discovery Center GmbH, D-44227 Dortmund, Germany.
Heiko MullerLead Discovery Center GmbH, D-44227 Dortmund, Germany.
Anke UngerLead Discovery Center GmbH, D-44227 Dortmund, Germany.
Hussein N RubaiySchool of Medicine, University of Leeds, Leeds, LS2 9JT, England, UK.
Ilka MatharInstitute of Pharmacology, Universität Heidelberg, D-69120 Heidelberg, Germany.
Klaus DinkelLead Discovery Center GmbH, D-44227 Dortmund, Germany.
Peter NussbaumerLead Discovery Center GmbH, D-44227 Dortmund, Germany.
Bert KleblLead Discovery Center GmbH, D-44227 Dortmund, Germany.
Marc FreichelInstitute of Pharmacology, Universität Heidelberg, D-69120 Heidelberg, Germany.
Baptiste RodeSchool of Medicine, University of Leeds, Leeds, LS2 9JT, England, UK.
Sebastian TrainorSchool of Medicine, University of Leeds, Leeds, LS2 9JT, England, UK.
Steven J ClapcoteSchool of Biomedical Sciences, University of Leeds, Leeds, LS2 9JT, UK.
Mathias ChristmannInstitute of Chemistry and Biochemistry, Freie Universität Berlin, 14195 Berlin, Germany.
Herbert WaldmannMax-Planck-Institut für Molekulare Physiologie, D-44227 Dortmund, Germany.
Syed Khawar AbbasSchool of Medicine, University of Leeds, Leeds, LS2 9JT, England, UK.
David J BeechSchool of Medicine, University of Leeds, Leeds, LS2 9JT, England, UK.
Naveen S VasudevSchool of Medicine, University of Leeds, Leeds, LS2 9JT, England, UK.
University of Leeds · GBLead Discovery Center (Germany) · DEFreie Universität Berlin · DEHeidelberg University · DEMax Planck Institute of Molecular Physiology · DE

Funding

KOMP2-Phase3 Production and Phenotyping by the DTCC Consortium TCP Transfer to UC DavisUM1OD023221 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KC KENT LLOYD · 2016 to 2026
$45.7M
Medical Research Council MC_PC_17165NIH HHS UM1 OD023221Wellcome Trust
6 · The paper itself

Abstract

(-)-Englerin A (EA) is a natural product which has potent cytotoxic effects on renal cell carcinoma cells and other types of cancer cell but not non-cancer cells. Although selectively cytotoxic to cancer cells, adverse reaction in mice and rats has been suggested. EA is a remarkably potent activator of ion channels formed by Transient Receptor Potential Canonical 4 and 5 proteins (TRPC4 and TRPC5) and TRPC4 is essential for EA-mediated cancer cell cytotoxicity. Here we specifically investigated the relevance of TRPC4 and TRPC5 to the adverse reaction. Injection of EA (2 mg.kg

Indexed as

breast cancerEwing’s sarcomarenal cancerTRPC4 channelsTRPC5 channels

Identifiers

PMID30038709
PMCPMC6049859
OpenAlexW2811308621

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.