Evidence map›Paper›PMID 25533033›Full record

ArticleBlood2015

Jun-regulated genes promote interaction of diffuse large B-cell lymphoma with the microenvironment.

Marzenna Blonska, Yifan Zhu, Hubert H Chuang, M James You, Kranthi Kunkalla, Francisco Vega, Xin Lin

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

45 citing papers in PubMed, 61 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

7 authors at 3 institutions in 1 country.

Marzenna BlonskaDepartment of Molecular and Cellular Oncology, Center for Inflammation and Cancer.
Yifan ZhuDepartment of Molecular and Cellular Oncology.
Hubert H ChuangDepartment of Nuclear Medicine, and.
M James YouCenter for Inflammation and Cancer, Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX;
Kranthi KunkallaDepartment of Pathology, Sylvester Cancer Center, University of Miami, Miami, FL; and.
Francisco VegaDepartment of Pathology, Sylvester Cancer Center, University of Miami, Miami, FL; and.
Xin LinDepartment of Molecular and Cellular Oncology, Center for Inflammation and Cancer, Cancer Biology Program, The University of Texas Graduate School of Biomedical Sciences, Houston, TX.
Sylvester Comprehensive Cancer Center · USThe University of Texas MD Anderson Cancer Center · USUniversity of Miami · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
The function of CARD9 in innate immune responsesR01AI050848 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, XIN · 2002 to 2012
$2.7M
T Cell receptor-induced NF-kB and JNK activationR01GM065899 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, XIN · 2002 to 2011
$2.5M
CARMA3-mediated NF-kappaB activation in GPCR signaling pathwaysR01GM079451 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, XIN · 2007 to 2010
$1.4M
CHARACTERIZATION AND TARGETED THERAPY OF T-ALL DEFICIENT FOR PTEN AND INK4A/ARFR01CA164346 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YOU, M. JAMES · 2012 to 2015
$1.2M
NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA164346NIAID NIH HHS R01 AI050848NIAID NIH HHS R01AI050848NIGMS NIH HHS R01 GM065899NIGMS NIH HHS R01GM065899NIGMS NIH HHS R01 GM079451
6 · The paper itself

Abstract

Diffuse large B-cell lymphoma (DLBCL) is an aggressive disease with a high proliferation rate. However, the molecular and genetic features that drive the aggressive clinical behavior of DLBCL are not fully defined. Here, we have demonstrated that activated Jun signaling is a frequent event in DLBCL that promotes dissemination of malignant cells. Downregulation of Jun dramatically reduces lymphoma cell adhesion to extracellular matrix proteins, subcutaneous tumor size in nude mice, and invasive behavior, including bone marrow infiltration and interaction with bone marrow stromal cells. Furthermore, using a combination of RNA interference and gene expression profiling, we identified Jun target genes that are associated with disseminated lymphoma. Among them, ITGAV, FoxC1, and CX3CR1 are significantly enriched in patients with 2 or more extranodal sites. Our results point to activated Jun signaling as a major driver of the aggressive phenotype of DLBCL.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell AdhesionCell Line, TumorExtracellular Matrix ProteinsGene Expression ProfilingGene Knockdown TechniquesHumansLymphoma, Large B-Cell, DiffuseMice, NudeProto-Oncogene Proteins c-junSignal TransductionTranscription Factor AP-1Transcription FactorsExtracellular Matrix ProteinsJunB protein, mouseProto-Oncogene Proteins c-junTranscription Factor AP-1Transcription Factors

Identifiers

PMID25533033
PMCPMC4319238
OpenAlexW2016956212

What OpenQuestion holds

Textmetadata
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.