Evidence map›Paper›PMID 30630973›Full record

ArticleHaematologica2019

LEF-1 drives aberrant β-catenin nuclear localization in myeloid leukemia cells.

Rhys G Morgan, Jenna Ridsdale, Megan Payne, Kate J Heesom, Marieangela C Wilson, Andrew Davidson, Alexander Greenhough, Sara Davies, Ann C Williams, Allison Blair and 3 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 56 citations in OpenAlex.

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  14. Emerging roles of MITF as a crucial regulator of immunity.Experimental & molecular medicine · 2024
    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

13 authors at 4 institutions in 2 countries.

Rhys G MorganSchool of Life Sciences, University of Sussex, Brighton, UK darley@cardiff.ac.uk rhys.morgan@sussex.ac.uk.
Jenna RidsdaleDepartment of Haematology, Division of Cancer and Genetics, School of Medicine, Cardiff University, UK.
Megan PayneSchool of Life Sciences, University of Sussex, Brighton, UK.
Kate J HeesomUniversity of Bristol Proteomics Facility, UK.
Marieangela C WilsonUniversity of Bristol Proteomics Facility, UK.
Andrew DavidsonSchool of Life Sciences, University of Sussex, Brighton, UK.
Alexander GreenhoughSchool of Life Sciences, University of Sussex, Brighton, UK.
Sara DaviesDepartment of Haematology, Division of Cancer and Genetics, School of Medicine, Cardiff University, UK.
Ann C WilliamsSchool of Life Sciences, University of Sussex, Brighton, UK.
Allison BlairSchool of Life Sciences, University of Sussex, Brighton, UK.
Marian L WatermanDepartment of Microbiology and Molecular Genetics, University of California, Irvine, CA, USA.
Alex TonksDepartment of Haematology, Division of Cancer and Genetics, School of Medicine, Cardiff University, UK.
Richard L DarleyDepartment of Haematology, Division of Cancer and Genetics, School of Medicine, Cardiff University, UK darley@cardiff.ac.uk rhys.morgan@sussex.ac.uk.
University of Sussex · GBCardiff University · GBUniversity of Bristol · GBUniversity of California, Irvine · US

Funding

Cancer Research UK 11975
6 · The paper itself

Abstract

Canonical Wnt/β-catenin signaling is frequently dysregulated in myeloid leukemias and is implicated in leukemogenesis. Nuclear-localized β-catenin is indicative of active Wnt signaling and is frequently observed in acute myeloid leukemia (AML) patients; however, some patients exhibit little or no nuclear β-catenin even where cytosolic β-catenin is abundant. Control of the subcellular localization of β-catenin therefore represents an additional mechanism regulating Wnt signaling in hematopoietic cells. To investigate the factors mediating the nuclear-localization of β-catenin, we carried out the first nuclear/cytoplasmic proteomic analysis of the β-catenin interactome in myeloid leukemia cells and identified putative novel β-catenin interactors. Comparison of interacting factors between Wnt-responsive cells (high nuclear β-catenin)

Indexed as

beta CateninBiomarkers, TumorCell NucleusGene Expression Regulation, NeoplasticHumansLeukemia, Myeloid, AcuteLymphoid Enhancer-Binding Factor 1Myelodysplastic SyndromesProtein Interaction Domains and MotifsProteomeRNA, Small InterferingTranscriptional ActivationTumor Cells, CulturedWnt1 Proteinbeta CateninBiomarkers, TumorCTNNB1 protein, humanLEF1 protein, humanLymphoid Enhancer-Binding Factor 1ProteomeRNA, Small InterferingWnt1 ProteinWNT1 protein, human

Identifiers

PMID30630973
PMCPMC6601079
OpenAlexW2910977478

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.