Evidence map›Paper›PMID 33349639›Full record

ArticleNature communications2020

The epigenetic regulator Mll1 is required for Wnt-driven intestinal tumorigenesis and cancer stemness.

Johanna Grinat, Julian Heuberger, Ramon Oliveira Vidal, Neha Goveas, Frauke Kosel, Antoni Berenguer-Llergo, Andrea Kranz, Annika Wulf-Goldenberg, Diana Behrens, Bálint Melcher and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.1field-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

46 citing papers in PubMed, 57 citations in OpenAlex.

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  10. Epigenetic regulation of cancer stemness.Signal transduction and targeted therapy · 2025
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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

15 authors at 5 institutions in 2 countries.

Johanna GrinatCancer Research Program, Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Society, 13125, Berlin, Germany.ORCID 0000-0003-0152-4941
Julian HeubergerCancer Research Program, Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Society, 13125, Berlin, Germany. julian.heuberger@charite.de.ORCID 0000-0001-7205-732X
Ramon Oliveira VidalLaboratory of Functional Genomics, Nutrigenomics and Systems Biology, Scientific Genomics Platforms, Max Delbrück Center for Molecular Medicine (BIMSB/BIH), 13092, Berlin, Germany.ORCID 0000-0003-4217-2014
Neha GoveasBiotechnology Center, Center for Molecular and Cellular Bioengineering, Technische Universität Dresden, 01307, Dresden, Germany.ORCID 0000-0002-2531-5514
Frauke KoselCancer Research Program, Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Society, 13125, Berlin, Germany.
Antoni Berenguer-LlergoBiostatistics and Bioinformatics Unit, Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID 0000-0002-3742-8161
Andrea KranzBiotechnology Center, Center for Molecular and Cellular Bioengineering, Technische Universität Dresden, 01307, Dresden, Germany.
Annika Wulf-GoldenbergExperimental Pharmacology & Oncology (EPO), 13125, Berlin, Germany.
Diana BehrensExperimental Pharmacology & Oncology (EPO), 13125, Berlin, Germany.
Bálint MelcherInstitute for Pathology, Klinikum Bayreuth, 95445, Bayreuth, Germany.
Sascha SauerLaboratory of Functional Genomics, Nutrigenomics and Systems Biology, Scientific Genomics Platforms, Max Delbrück Center for Molecular Medicine (BIMSB/BIH), 13092, Berlin, Germany.ORCID 0000-0002-4794-3693
Michael ViethInstitute for Pathology, Klinikum Bayreuth, 95445, Bayreuth, Germany.
Eduard BatlleInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, Barcelona, Spain.
A Francis StewartBiotechnology Center, Center for Molecular and Cellular Bioengineering, Technische Universität Dresden, 01307, Dresden, Germany.
Walter BirchmeierCancer Research Program, Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Society, 13125, Berlin, Germany. wbirch@mdc-berlin.de.ORCID 0000-0003-1173-0829
Max Delbrück Center · DETechnische Universität Dresden · DEBayreuth Medical Center · DEInstitució Catalana de Recerca i Estudis Avançats · ESInstitute for Research in Biomedicine · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wnt/β-catenin signaling is crucial for intestinal carcinogenesis and the maintenance of intestinal cancer stem cells. Here we identify the histone methyltransferase Mll1 as a regulator of Wnt-driven intestinal cancer. Mll1 is highly expressed in Lgr5

Indexed as

Epigenesis, GeneticWnt Signaling PathwayAnimalsbeta CateninCarcinogenesisCell DifferentiationCell Line, TumorColonic NeoplasmsGene Expression Regulation, NeoplasticHEK293 CellsHistone-Lysine N-MethyltransferaseHistonesHumansIntestinesLysineMethylationbeta CateninHistone-Lysine N-MethyltransferaseHistonesKMT2A protein, humanLGR5 protein, humanLysineMyeloid-Lymphoid Leukemia ProteinPolycomb Repressive Complex 2Receptors, G-Protein-Coupled

Identifiers

PMID33349639
PMCPMC7752919
OpenAlexW3112759074

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.