Evidence map›Paper›PMID 36435864›Full record

ArticleBMC research notes2022

TAK1-inhibitors did not reduce disease burden in a Vκ*MYC model of multiple myeloma.

Erling Håland, Ingrid Nyhus Moen, Esten N Vandsemb, Kristian K Starheim

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 2 institutions in 1 country.

Erling HålandCEMIR Centre of Molecular Inflammation Research, IKOM, NTNU, Trondheim, Norway.
Ingrid Nyhus MoenCEMIR Centre of Molecular Inflammation Research, IKOM, NTNU, Trondheim, Norway.
Esten N VandsembDepartment of Clinical and Molecular Medicine, NTNU, Trondheim, Norway.
Kristian K StarheimCEMIR Centre of Molecular Inflammation Research, IKOM, NTNU, Trondheim, Norway. Kristian.starheim@ntnu.no.ORCID http://orcid.org/0000-0003-4598-1896
Norwegian University of Science and Technology · NOSt Olav's University Hospital · NO

Funding

Helse Midt-Norge Helse Midt-NorgeKreftforeningen 6799133Norges Forskningsråd 2223255/F50
6 · The paper itself

Abstract

objectiveMultiple myeloma is a haematological malignancy characterized by proliferation of monoclonal plasma cells in the bone marrow. Development of resistance and minimal residual disease remain challenging in the treatment of multiple myeloma. Transforming growth factor-β activated kinase 1 (TAK1) has recently gained attention as a potential drug target in multiple myeloma. This study aimed at determining the in vivo effects of TAK1-inhibitors in a Vκ*MYC multiple myeloma mouse model.

resultsWe treated mice carrying Vκ*MYC multiple myeloma cells with the TAK1-inhibitors 5Z-7-oxozeaenol and NG25. There were tendencies towards increased survival for both inhibitors, but only NG25 prolonged survival significantly. However, this effect was limited, and no differences in disease burden were observed for any of the treatments. In conclusion, although TAK1-inhibitors might prolong survival somewhat, they do not prevent disease in the Vκ*MYC mouse model of multiple myeloma.

Indexed as

Multiple MyelomaZearalenoneAnimalsCost of IllnessMiceZearalenone5Z-7Haematological malignancyMultiple myelomaNG25TAK1

Identifiers

PMID36435864
PMCPMC9701378
OpenAlexW4310295523

What OpenQuestion holds

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Registered trials

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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.