Evidence map›Paper›PMID 34676048›Full record

ArticleOncotarget2021

TAK1-inhibitors are cytotoxic for multiple myeloma cells alone and in combination with melphalan.

Erling Håland, Ingrid Nyhus Moen, Elias Veidal, Hanne Hella, Kristine Misund, Tobias S Slørdahl, Kristian K Starheim

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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 1 institution 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.
Elias VeidalCEMIR Centre of Molecular Inflammation Research, IKOM, NTNU, Trondheim, Norway.
Hanne HellaDepartment of Clinical and Molecular Medicine, NTNU, Trondheim, Norway.
Kristine MisundDepartment of Clinical and Molecular Medicine, NTNU, Trondheim, Norway.
Tobias S SlørdahlDepartment of Clinical and Molecular Medicine, NTNU, Trondheim, Norway.
Kristian K StarheimCEMIR Centre of Molecular Inflammation Research, IKOM, NTNU, Trondheim, Norway.
St Olav's University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is an incurable cancer caused by malignant transformation of plasma cells. Transforming growth factor-β activated kinase 1 (MAP3K7, TAK1) is a major regulator of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) and mitogen-activated protein kinase (MAPK) signaling. Both NF-κB and MAPK control expression of genes with vital roles for drug resistance in MM. TAK1 is an attractive drug target as it switches these survival pathways to cell death. Our analysis showed that patients with high

Indexed as

apoptosiscancer treatmentmultiple myelomaNF-κBTAK1

Identifiers

PMID34676048
PMCPMC8522844
OpenAlexW3206371817

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.