Evidence map›Paper›PMID 23848362›Full record

ArticleBiochemistry2013

Off-target effects of MEK inhibitors.

Eric M Wauson, Marcy L Guerra, Barbara Barylko, Joseph P Albanesi, Melanie H Cobb

Open access · greenAbstract read
In one paragraph

Article in Biochemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 47 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Eric M WausonDepartment of Pharmacology, University of Texas Southwestern Medical Center , Dallas, Texas 75390-9041, United States.
Marcy L Guerra
Barbara Barylko
Joseph P Albanesi
Melanie H Cobb
The University of Texas Southwestern Medical Center · US

Funding

MAP Kinse in Islet FunctionR01DK055310 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1998 to 2014
$3.4M
NIDDK NIH HHS DK55310NIDDK NIH HHS R01 DK055310
6 · The paper itself

Abstract

The mitogen-activated protein kinases (MAPKs) ERK1/2 regulate numerous cellular processes, including gene transcription, proliferation, and differentiation. The only known substrates of the MAP2Ks MEK1/2 are ERK1/2; thus, MEK inhibitors PD98059, U0126, and PD0325901 have been important tools in determining the functions of ERK1/2. By using these inhibitors and genetically manipulating MEK, we found that ERK1/2 activation is neither sufficient nor necessary for regulated secretion of insulin from pancreatic β cells or secretion of epinephrine from chromaffin cells. We show that both PD98059 and U0126 reduce agonist-induced entry of calcium into cells in a manner independent of their ability to inhibit ERK1/2. Caution should be used when interpreting results from experiments using these compounds.

Indexed as

AnimalsBenzamidesButadienesCalciumCell LineChromaffin CellsDiphenylamineEpinephrineFlavonoidsInsulinInsulin-Secreting CellsInsulin SecretionMAP Kinase Kinase 1MAP Kinase Kinase 2MiceMitogen-Activated Protein Kinase 32-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-oneBenzamidesButadienesCalciumDiphenylamineEpinephrineFlavonoidsInsulinMap2k1 protein, mouseMap2k2 protein, mouseMAP Kinase Kinase 1MAP Kinase Kinase 2mirdametinibMitogen-Activated Protein Kinase 3NitrilesProtein Kinase InhibitorsU 0126

Identifiers

PMID23848362
PMCPMC3859837
OpenAlexW2001313970

What OpenQuestion holds

Textmetadata
LicenceTDM
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.