Evidence map›Paper›PMID 32079091›Full record

ArticleCancers2020

Exon-4 Mutations in KRAS Affect MEK/ERK and PI3K/AKT Signaling in Human Multiple Myeloma Cell Lines.

Susann Weißbach, Sofia Catalina Heredia-Guerrero, Stefanie Barnsteiner, Lukas Großhans, Jochen Bodem, Hanna Starz, Christian Langer, Silke Appenzeller, Stefan Knop, Torsten Steinbrunn and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Expression ofInternational journal of molecular sciences · 2025
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  12. Blood research · 2020
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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

16 authors at 4 institutions in 1 country.

Susann WeißbachInstitute of Pathology, University of Würzburg, Josef-Schneider-Str. 2, 97080 Würzburg, Germany.
Sofia Catalina Heredia-GuerreroInstitute of Pathology, University of Würzburg, Josef-Schneider-Str. 2, 97080 Würzburg, Germany.
Stefanie BarnsteinerInstitute of Pathology, University of Würzburg, Josef-Schneider-Str. 2, 97080 Würzburg, Germany.
Lukas GroßhansComprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Josef-Schneider-Str. 6, 97080 Würzburg, Germany.
Jochen BodemInstitute of Virology and Immunobiology, University of Würzburg, Versbacher Str. 7, 97078 Würzburg, Germany.ORCID 0000-0003-1908-4091
Hanna StarzInstitute of Pathology, University of Würzburg, Josef-Schneider-Str. 2, 97080 Würzburg, Germany.
Christian LangerDepartment of Internal Medicine III, University Hospital of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany.
Silke AppenzellerComprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Josef-Schneider-Str. 6, 97080 Würzburg, Germany.
Stefan KnopDepartment of Internal Medicine II, University Hospital Würzburg, Oberdürrbacher Str. 6, 97080 Würzburg, Germany.
Torsten SteinbrunnDepartment of Internal Medicine II, University Hospital Würzburg, Oberdürrbacher Str. 6, 97080 Würzburg, Germany.
Simone RostInstitute of Human Genetics, Biocenter, University of Würzburg, Am Hubland, 97074 Würzburg, Germany.
Hermann EinseleDepartment of Internal Medicine II, University Hospital Würzburg, Oberdürrbacher Str. 6, 97080 Würzburg, Germany.
Ralf Christian BargouComprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Josef-Schneider-Str. 6, 97080 Würzburg, Germany.
Andreas RosenwaldInstitute of Pathology, University of Würzburg, Josef-Schneider-Str. 2, 97080 Würzburg, Germany.
Thorsten StühmerComprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Josef-Schneider-Str. 6, 97080 Würzburg, Germany.
Ellen LeichInstitute of Pathology, University of Würzburg, Josef-Schneider-Str. 2, 97080 Würzburg, Germany.
University of Würzburg · DEComprehensive Cancer Center Mainfranken · DEUniversitätsklinikum Würzburg · DEUniversity Hospital Ulm · DE

Funding

Deutsche Forschungsgemeinschaft KFO216Deutsche Krebshilfe 70112693Wilhelm Sander-Stiftung 2014.903.1
6 · The paper itself

Abstract

Approximately 20% of multiple myeloma (MM) cases harbor a point mutation in

Indexed as

AKT-signalingamplicon sequencingKRASMEK/ERK-signalingmultiple myeloma

Identifiers

PMID32079091
PMCPMC7072554
OpenAlexW3006486946

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.