Evidence map›Paper›PMID 36499034›Full record

ArticleInternational journal of molecular sciences2022

Heterogeneity of Patient-Derived Acute Myeloid Leukemia Cells Subjected to SYK In Vitro Inhibition.

Marte Karen Brattås, Anette Lodvir Hemsing, Kristin Paulsen Rye, Kimberley Joanne Hatfield, Håkon Reikvam

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 6 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

5 authors at 2 institutions in 1 country.

Marte Karen BrattåsDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway.
Anette Lodvir HemsingDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway.ORCID 0000-0002-1567-1099
Kristin Paulsen RyeDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway.
Kimberley Joanne HatfieldDepartment of Immunology and Transfusion Medicine, Haukeland University Hospital, 5021 Bergen, Norway.
Håkon ReikvamDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway.ORCID 0000-0001-5439-8411
Haukeland University Hospital · NOUniversity of Bergen · NO

Funding

Helse Vest NAthe Norwegian Cancer Society NAthe Rotary Foundation NA
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is an aggressive hematological malignancy with a dismal prognosis. The cytoplasmic spleen tyrosine kinase (SYK) is highly expressed by hematopoietic cells and has emerged as a potential therapeutic target. In this study, we evaluated the in vitro antileukemic effects of five SYK inhibitors, fostamatinib, entospletinib, cerdulatinib, TAK-659, and RO9021, in a consecutive AML patient cohort. All inhibitors demonstrated a concentration-dependent antiproliferative effect, although there was considerable heterogeneity among patients. For fostamatinib and TAK-659, the antiproliferative effects were significantly higher in

Indexed as

Leukemia, Myeloid, AcuteProtein Kinase InhibitorsAminopyridinesfms-Like Tyrosine Kinase 3HumansMorpholinesPyridazinesPyrimidinesSignal TransductionSyk Kinase6-(2-aminocyclohexylamino)-4-(5,6-dimethylpyridin-2-ylamino)pyridazine-3-carboxylic acid amideAminopyridinesfms-Like Tyrosine Kinase 3fostamatinibMorpholinesProtein Kinase InhibitorsPyridazinesPyrimidinesSyk KinaseSYK protein, humanacute myeloid leukemia (AML)apoptosiscytokinesproliferationspleen tyrosine kinase (SYK)

Identifiers

PMID36499034
PMCPMC9737311
OpenAlexW4310038910

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.