Evidence map›Paper›PMID 39303915›Full record

ReviewThe Journal of biological chemistry2024

Histone methyltransferase KMT2A: Developmental regulation to oncogenic transformation.

Jayme Ogino, Yali Dou

Abstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

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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

2 authors.

Jayme OginoDivision of Pediatric Hematology-Oncology, Children's Hospital Los Angeles, Los Angeles, California, USA; Department of Medicine, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California, USA.
Yali DouDepartment of Medicine, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California, USA. Electronic address: yalidou@usc.edu.

Funding

Non-canonical function of transcription cofactor MLL1 in cancerR01CA287625 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Yali Dou · 2024 to 2026
$1.5M
NCI NIH HHS R01 CA287625
6 · The paper itself

Abstract

Our current understanding of epigenetic regulation is deeply rooted in the founding contributions of Dr C. David Allis. In 2002, Allis and colleagues first characterized the lysine methyltransferase activity of the mammalian KMT2A (MLL1), a paradigm-shifting discovery that brings epigenetic dysregulation into focus for many human diseases that carry KMT2A mutations. This review will discuss the current understanding of the multifaceted roles of KMT2A in development and disease, which has paved the way for innovative and upcoming approaches to cancer therapy.

Indexed as

Cell Transformation, NeoplasticHistone-Lysine N-MethyltransferaseMyeloid-Lymphoid Leukemia ProteinAnimalsEpigenesis, GeneticHumansNeoplasmsHistone-Lysine N-MethyltransferaseKMT2A protein, humanMyeloid-Lymphoid Leukemia Proteincancer therapydevelopmentepigeneticshistone methylationKMT2AleukemiaMLL

Identifiers

PMID39303915
PMCPMC11736124

What OpenQuestion holds

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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.