Evidence map›Paper›PMID 40849328›Full record

ArticleNature communications2025

NSUN2 facilitates DICER cleavage of DNA damage-associated R-loops to promote repair.

Adele Alagia, Kamal Ajit, Arianna Di Fazio, Qilin Long, Monika Gullerova

Abstract read
In one paragraph

Article in Nature communications, 2025. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Roles and mechanisms of NSUN2-mediated RNA mFrontiers in immunology · 2025
    Review
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.

Adele AlagiaSir William Dunn School of Pathology, South Parks Road, Oxford, UK.ORCID http://orcid.org/0000-0001-6421-7733
Kamal AjitSir William Dunn School of Pathology, South Parks Road, Oxford, UK.
Arianna Di FazioSir William Dunn School of Pathology, South Parks Road, Oxford, UK.
Qilin LongSir William Dunn School of Pathology, South Parks Road, Oxford, UK.
Monika GullerovaSir William Dunn School of Pathology, South Parks Road, Oxford, UK. monika.gullerova@path.ox.ac.uk.ORCID http://orcid.org/0000-0002-4512-2779

Funding

Cancer Research UK (CRUK) BVR01170RCUK | Medical Research Council (MRC) BVR02590
6 · The paper itself

Abstract

DNA integrity is constantly challenged by both endogenous and exogenous damaging agents, resulting in various forms of damage. Failure to repair DNA accurately leads to genomic instability, a hallmark of cancer. Distinct pathways exist to repair different types of DNA damage. Double-strand breaks (DSBs) represent a particularly severe form of damage, due to the physical separation of DNA strands. The repair of DSBs requires the activity of RNA Polymerase II (RNAPII) and the generation of Damage-responsive transcripts (DARTs). Here we show that the RNA m

Indexed as

DEAD-box RNA HelicasesDNA RepairMethyltransferasesRibonuclease IIIR-Loop StructuresDNA Breaks, Double-StrandedDNA DamageHumansRNA Polymerase IIDEAD-box RNA HelicasesDICER1 protein, humanMethyltransferasesNSUN2 protein, humanRibonuclease IIIRNA Polymerase II

Identifiers

PMID40849328
PMCPMC12374970

What OpenQuestion holds

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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.