Evidence map›Paper›PMID 31277464›Full record

ArticleJournal of clinical medicine2019

High Constitutive Cytokine Release by Primary Human Acute Myeloid Leukemia Cells Is Associated with a Specific Intercellular Communication Phenotype.

Håkon Reikvam, Elise Aasebø, Annette K Brenner, Sushma Bartaula-Brevik, Ida Sofie Grønningsæter, Rakel Brendsdal Forthun, Randi Hovland, Øystein Bruserud

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  5. Biomedicines · 2022
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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

8 authors at 2 institutions in 1 country.

Håkon ReikvamDepartment of Clinical Science, University of Bergen, 5020,Bergen, Norway. Hakon.Reikvam@med.uib.no.ORCID 0000-0001-5439-8411
Elise AasebøDepartment of Clinical Science, University of Bergen, 5020,Bergen, Norway.ORCID 0000-0002-6939-8059
Annette K BrennerDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.
Sushma Bartaula-BrevikDepartment of Clinical Science, University of Bergen, 5020,Bergen, Norway.
Ida Sofie GrønningsæterDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.
Rakel Brendsdal ForthunDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.
Randi HovlandDepartment of Medical Genetics, Haukeland University Hospital, 5021 Bergen, Norway.
Øystein BruserudDepartment of Clinical Science, University of Bergen, 5020,Bergen, Norway.
Haukeland University Hospital · NOUniversity of Bergen · NO

Funding

Helse Vest Helse VestThe norwegian cancer society The norwegian cancer society
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogeneous disease, and this heterogeneity includes the capacity of constitutive release of extracellular soluble mediators by AML cells. We investigated whether this capacity is associated with molecular genetic abnormalities, and we compared the proteomic profiles of AML cells with high and low release. AML cells were derived from 71 consecutive patients that showed an expected frequency of cytogenetic and molecular genetic abnormalities. The constitutive extracellular release of 34 soluble mediators (CCL and CXCL chemokines, interleukins, proteases, and protease regulators) was investigated for an unselected subset of 62 patients, and they could be classified into high/intermediate/low release subsets based on their general capacity of constitutive secretion.

Indexed as

acute myeloid leukemiacytokinesdifferentiationgene mutationsintegrinproteomic profileRAC1SYK

Identifiers

PMID31277464
PMCPMC6678419
OpenAlexW2955011564

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.