Evidence map›Paper›PMID 23647456›Full record

ArticleBritish journal of haematology2013

TRIM13 (RFP2) downregulation decreases tumour cell growth in multiple myeloma through inhibition of NF Kappa B pathway and proteasome activity.

Moshe E Gatt, Kohichi Takada, Mala Mani, Mikael Lerner, Marjorie Pick, Teru Hideshima, Daniel E Carrasco, Alexei Protopopov, Elena Ivanova, Olle Sangfelt and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of haematology, 2013. 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
0.6field-weighted citation impact, top 30% 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, 25 citations in OpenAlex.

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  14. TRIM proteins in blood cancers.Journal of cell communication and signaling · 2018
    Review
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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

15 authors at 5 institutions in 4 countries.

Moshe E GattDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Kohichi Takada
Mala Mani
Mikael Lerner
Marjorie Pick
Teru Hideshima
Daniel E Carrasco
Alexei Protopopov
Elena Ivanova
Olle Sangfelt
Dan Grandér
Bart Barlogie
John D Shaughnessy
Kenneth C Anderson
Daniel R Carrasco
Harvard University · USBrigham and Women's Hospital · USKarolinska University Hospital · SEHebrew University of Jerusalem · ILUniversity of Arkansas for Medical Sciences · US

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
Targeting Myeloma Cell-Host Bone Marrow InteractionsP01CA078378 · NCI · DANA-FARBER CANCER INSTITUTE · PI RITZ, JEROME · 1998 to 2014
$26.2M
Mining B-catenin/BCL9 transcriptional complex for Multiple Myeloma therapeuticsR01CA151391 · NCI · DANA-FARBER CANCER INST · PI CARRASCO, RUBEN D · 2010 to 2014
$1.7M
Prospective evaluation of IGF and IL-6 Dysregulation and Multiple MyelomaR01CA127435 · NCI · WASHINGTON UNIVERSITY · PI COLDITZ, GRAHAM A. · 2007 to 2010
$1.4M
NCI NIH HHS P01 CA078378NCI NIH HHS P01 CA155258NCI NIH HHS P0 CA78378NCI NIH HHS P50 CA100707NCI NIH HHS R01 CA127435NCI NIH HHS R01 CA151391NCI NIH HHS R0 CA127435
6 · The paper itself

Abstract

Multiple myeloma (MM) is an incurable neoplasm caused by proliferation of malignant plasma cells in the bone marrow (BM). MM is characterized frequently by a complete or partial deletion of chromosome 13q14, seen in more than 50% of patients at diagnosis. Within this deleted region the tripartite motif containing 13 (TRIM13, also termed RFP2) gene product has been proposed to be a tumour suppressor gene (TSG). Here, we show that low expression levels of TRIM13 in MM are associated with chromosome 13q deletion and poor clinical outcome. We present a functional analysis of TRIM13 using a loss-of-function approach, and demonstrate that TRIM13 downregulation decreases tumour cell survival as well as cell cycle progression and proliferation of MM cells. In addition, we provide evidence for the involvement of TRIM13 downregulation in inhibiting the NF kappa B pathway and the activity of the 20S proteasome. Although this data does not support a role of TRIM13 as a TSG, it substantiates important roles of TRIM13 in MM tumour survival and proliferation, underscoring its potential role as a novel target for therapeutic intervention.

Indexed as

ApoptosisCell CycleCell DivisionCell Line, TumorCell SurvivalChromosome DeletionChromosomes, Human, Pair 13DNA-Binding ProteinsDown-RegulationGene Expression ProfilingGene Knockdown TechniquesHumansMultiple MyelomaNF-kappa BProteasome Endopeptidase ComplexTumor Suppressor ProteinsDNA-Binding ProteinsNF-kappa BProteasome Endopeptidase ComplexTRIM13 protein, humanTumor Suppressor Proteins13qmyelomaproliferationproteasomeTRIM13 (RFP2)

Identifiers

PMID23647456
PMCPMC3709857
OpenAlexW2084802784

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.