Evidence map›Paper›PMID 20117835›Full record

ArticleLeukemia research2010

Inhibition of MEK/ERK1/2 sensitizes lymphoma cells to sorafenib-induced apoptosis.

Tri K Nguyen, Nicholas Jordan, Jonathan Friedberg, Richard I Fisher, Paul Dent, Steven Grant

Abstract read
In one paragraph

Article in Leukemia research, 2010. 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
1.9field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
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  4. TheInternational journal of molecular sciences · 2019
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  8. Modulation of Navitoclax Sensitivity by Dihydroartemisinin-Mediated MCL-1 Repression in BCR-ABLClinical cancer research : an official journal of the American Association for Cancer Research · 2017
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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

6 authors at 2 institutions in 1 country.

Tri K NguyenDepartment of Medicine, Institute of Molecular Medicine and the Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, United States.
Nicholas Jordan
Jonathan Friedberg
Richard I Fisher
Paul Dent
Steven Grant
Virginia Commonwealth University · USUniversity of Rochester · US

Funding

SPORE in LymphomaP50CA130805 · NCI · UNIVERSITY OF ROCHESTER · PI FISHER, RICHARD I · 2008 to 2012
$11.7M
SIGNALING PATHWAYS REGULATING EPITHELIAL CELL SURVIVALR01DK052825 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 1999 to 2013
$3.3M
NF-kappaB Inhibitors and Differentiation-Inducers in LeukemiaR01CA093738 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRANT, STEVEN · 2002 to 2011
$2.4M
Checkpoint Abrogation and MEK 1/2 Inhibition in MyelomaR01CA100866 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRANT, STEVEN · 2003 to 2013
$2.2M
Promotion of Nucleoside Analog Induced Apoptosis by HDIsR01CA063753 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRANT, STEVEN · 1994 to 2008
$2.2M
OSU-03012 therapy for glioblastomaR01CA141703 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 2010 to 2014
$1.5M
Lapatinib and Obatoclax combination therapyR01CA150214 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 2010 to 2014
$1.5M
NCI NIH HHS 1P50 CA130805NCI NIH HHS CA100866NCI NIH HHS CA63753NCI NIH HHS CA93738NCI NIH HHS P50 CA130805NCI NIH HHS R01 CA063753NCI NIH HHS R01 CA093738NCI NIH HHS R01 CA100866NCI NIH HHS R01 CA141703NCI NIH HHS R01 CA150214NIDDK NIH HHS R01 DK052825
6 · The paper itself

Abstract

Interactions between the multi-kinase inhibitor sorafenib and MEK1/2 inhibitors were investigated in DLBCL cells. Sorafenib (3-10 microM) triggered apoptosis in multiple GC and ABC lymphoma cells. Unexpectedly, sorafenib did not cause sustained ERK1/2 inactivation, and in SUDHL-6 and -16 cells, triggered ERK1/2 activation. Marginally toxic MEK1/2 inhibitor concentrations (5 microM PD184352) abrogated ERK1/2 activation in sorafenib-treated cells and synergistically potentiated apoptosis. MEK1 shRNA transfection also significantly increased sorafenib-mediated lethality. Sorafenib/PD184352 co-administration accelerated Mcl-1 down-regulation without up-regulating Bim(EL). Finally, ectopic Mcl-1 expression attenuated sorafenib/PD184352-mediated apoptosis. Together, these findings provide a theoretical basis for potentiating sorafenib anti-lymphoma activity by MEK1/2 inhibitors.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsApoptosisBenzamidesBenzenesulfonatesBlotting, WesternCell Line, TumorEnzyme InhibitorsExtracellular Signal-Regulated MAP KinasesHumansLymphoma, Large B-Cell, DiffuseMAP Kinase Kinase KinasesNiacinamidePhenylurea CompoundsPyridinesReverse Transcriptase Polymerase Chain ReactionSignal Transduction2-(2-chloro-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluorobenzamideBenzamidesBenzenesulfonatesEnzyme InhibitorsExtracellular Signal-Regulated MAP KinasesMAP Kinase Kinase KinasesNiacinamidePhenylurea CompoundsPyridinesSorafenib

Identifiers

PMID20117835
PMCPMC3150480
OpenAlexW2145704036

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.