Evidence map›Paper›PMID 30931942›Full record

ArticleCell death & disease2019

The unfolded protein response modulators GSK2606414 and KIRA6 are potent KIT inhibitors.

Mohamed Mahameed, Thomas Wilhelm, Odai Darawshi, Akram Obiedat, Weiss-Sadan Tommy, Chetan Chintha, Thomas Schubert, Afshin Samali, Eric Chevet, Leif A Eriksson and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

53 citing papers in PubMed, 82 citations in OpenAlex.

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  19. Dual RNase activity of IRE1 as a target for anticancer therapies.Journal of cell communication and signaling · 2023
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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 at 5 institutions in 5 countries.

Mohamed MahameedInstitute for Drug Research, The Hebrew University of Jerusalem, Jerusalem, Israel.
Thomas WilhelmInstitute of Biochemistry and Molecular Immunology, Medical School, RWTH Aachen University, Aachen, Germany.
Odai DarawshiInstitute for Drug Research, The Hebrew University of Jerusalem, Jerusalem, Israel.
Akram ObiedatInstitute for Drug Research, The Hebrew University of Jerusalem, Jerusalem, Israel.
Weiss-Sadan TommyInstitute for Drug Research, The Hebrew University of Jerusalem, Jerusalem, Israel.
Chetan ChinthaApoptosis Research Centre, National University of Ireland Galway, Galway, H91 TK33, Ireland.
Thomas Schubert2bind GmbH, Am BioPark 11, 93053, Regensburg, Germany.
Afshin SamaliApoptosis Research Centre, National University of Ireland Galway, Galway, H91 TK33, Ireland.ORCID http://orcid.org/0000-0002-8610-8375
Eric ChevetINSERM U1242, Université de Rennes, Rennes, France.
Leif A ErikssonDepartment of Chemistry and Molecular Biology, University of Gothenburg, Göthenburg, Sweden.ORCID http://orcid.org/0000-0001-5654-3109
Michael HuberInstitute of Biochemistry and Molecular Immunology, Medical School, RWTH Aachen University, Aachen, Germany.
Boaz TiroshInstitute for Drug Research, The Hebrew University of Jerusalem, Jerusalem, Israel. boazt@ekmd.huji.ac.il.ORCID http://orcid.org/0000-0001-8067-6577
Hebrew University of Jerusalem · ILOllscoil na Gaillimhe – University of Galway · IERWTH Aachen University · DEInserm · FRUniversity of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IRE1, PERK, and ATF6 are the three transducers of the mammalian canonical unfolded protein response (UPR). GSK2606414 is a potent inhibitor of PERK, while KIRA6 inhibits the kinase activity of IRE1. Both molecules are frequently used to probe the biological roles of the UPR in mammalian cells. In a direct binding assay, GSK2606414 bound to the cytoplasmic domain of KIT with dissociation constants (K

Indexed as

AdenineCell SurvivaleIF-2 KinaseEndocytosisHEK293 CellsHep G2 CellsHumansImidazolesIndolesKineticsLysosomesNaphthalenesProto-Oncogene Proteins c-kitPyrazinesUnfolded Protein Response7-methyl-5-(1-((3-(trifluoromethyl)phenyl)acetyl)-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo(2,3-d)pyrimidin-4-amineAdenineeIF-2 KinaseImidazolesIndolesKIRA6NaphthalenesProto-Oncogene Proteins c-kitPyrazines

Identifiers

PMID30931942
PMCPMC6443726
OpenAlexW2931575706

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.