Evidence map›Paper›PMID 40145864›Full record

ArticleGenes, chromosomes & cancer2025

Discovery of Cis-Regulatory Mechanisms via Non-Coding Mutations in Acute Lymphoblastic Leukemia.

Efe Aydın, Eleanor L Woodward, Gladys Telliam Dushime, Rebeqa Gunnarsson, Henrik Lilljebjörn, Larissa H Moura-Castro, Thoas Fioretos, Bertil Johansson, Kajsa Paulsson, Minjun Yang

Abstract read
In one paragraph

Article in Genes, chromosomes & cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Efe AydınDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.
Eleanor L WoodwardDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.
Gladys Telliam DushimeDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.
Rebeqa GunnarssonDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.
Henrik LilljebjörnDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.ORCID 0000-0001-8703-1173
Larissa H Moura-CastroDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.ORCID 0000-0001-9063-5592
Thoas FioretosDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.
Bertil JohanssonDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.
Kajsa PaulssonDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.ORCID 0000-0001-7950-222X
Minjun YangDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.ORCID 0000-0002-3324-1498

Funding

BarncancerfondenCancerfondenCrafoordska StiftelsenGovernmental Funding of Clinical Research within the National Health ServiceVetenskapsrådet
6 · The paper itself

Abstract

The non-coding genome, constituting 98% of human DNA, remains largely unexplored, yet holds potential for identifying new biomarkers and therapeutic targets in acute lymphoblastic leukemia (ALL). In this study, we conducted a systematic analysis of recurrent somatic non-coding single nucleotide variants (SNVs) in pediatric B-cell precursor (BCP) ALL. We leveraged whole genome sequencing (WGS) data from 345 pediatric BCP ALL cases, representing all major genetic subtypes and identified 346 mutational hotspots that harbored somatic SNVs in at least three cases. Through the integration of paired RNA sequencing along with published ChIP-seq and ATAC-seq data, we found 128 non-coding hotspots associated with differentially expressed genes nearby, which were enriched for cis-regulatory elements, demonstrating the effectiveness of multi-omics integration in distinguishing pathogenic mutations from passengers. We identified one mutational hotspot that was associated with increased expression of the leukemia-associated gene NRAS in three primary ALLs. Micro-C analysis in the leukemia cell line demonstrated interactions between the hotspot region and NRAS regulatory elements. Dual luciferase assays indicated that the mutations disrupted regulatory interactions and CRISPR-mediated deletion of the region significantly upregulated NRAS, confirming the hypothesized regulatory link. Altogether, we provide new insights into the functional roles of non-coding mutations in leukemia.

Indexed as

MutationPrecursor Cell Lymphoblastic Leukemia-LymphomaRegulatory Sequences, Nucleic AcidCell Line, TumorChildFemaleGene Expression Regulation, LeukemicGTP PhosphohydrolasesHumansMaleMembrane ProteinsPolymorphism, Single NucleotideWhole Genome SequencingGTP PhosphohydrolasesMembrane ProteinsNRAS protein, humanB‐cell precursor acute lymphoblastic leukemiacis‐regulatory elementsleukemogenesismulti‐omicsnon‐coding mutations

Identifiers

PMID40145864
PMCPMC11949094

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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.