Evidence map›Paper›PMID 41519897›Full record

ArticleNature communications2026

Single-cell multiplex approaches deeply map ON-target CRISPR-genotoxicity and reveal its mitigation by palbociclib and long-term engraftment.

Julian Boutin, Sabrina Fayet, Victor Marin, Camille Bergès, Maude Riandière, Jérôme Toutain, Isabelle Lamrissi-Garcia, Chloé Thibault, David Cappellen, Sandrine Dabernat and 7 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

17 authors.

Julian Boutin *Univ Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.ORCID http://orcid.org/0000-0001-9948-4129
Sabrina Fayet *Univ Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.
Victor Marin *Univ Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.ORCID http://orcid.org/0009-0000-7439-192X
Camille Bergès *Univ Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.ORCID http://orcid.org/0000-0002-7773-3689
Maude RiandièreUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.
Jérôme ToutainUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.
Isabelle Lamrissi-GarciaUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.
Chloé ThibaultUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.ORCID http://orcid.org/0000-0002-9420-4180
David CappellenUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.ORCID http://orcid.org/0000-0002-9634-2595
Sandrine DabernatUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.
Arthur PouletUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France.ORCID http://orcid.org/0000-0002-2020-9085
Maëla FrancilletteINSERM US23, CNRS UAR 3655, AMMICa, Genomic Platform, Gustave Roussy Cancer Center, Villejuif, France.
Nathalie DroinINSERM US23, CNRS UAR 3655, AMMICa, Genomic Platform, Gustave Roussy Cancer Center, Villejuif, France.ORCID http://orcid.org/0000-0002-6099-5324
Christelle DebeissatEtablissement Français du Sang Nouvelle Aquitaine, Place Amélie Raba Léon, Bordeaux, France.
Philippe Brunet de la GrangeEtablissement Français du Sang Nouvelle Aquitaine, Place Amélie Raba Léon, Bordeaux, France.ORCID http://orcid.org/0000-0001-5002-6012
François Moreau-GaudryUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France. francois.moreau-gaudry@u-bordeaux.fr.ORCID http://orcid.org/0000-0003-1813-3939
Aurélie BedelUniv Bordeaux, INSERM, UMR 1312, BRIC (Bordeaux Institute of Oncology), Bordeaux, France. aurelie.bedel@u-bordeaux.fr.ORCID http://orcid.org/0000-0003-1226-1753

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome editing by CRISPR-Cas9-nuclease is promising for gene therapy. However, safety concerns remain. Monitoring ON-target genotoxicity is essential, especially to assay megabasic rearrangements at the targeted locus. Here, we developed a combined single-cell resolution approach with DNA sequencing focused on single nucleotide polymorphism (scSNP-DNAseq), micronuclei and LOH cytometry-reporter assays. This sensitive multiplexed strategy enables the sensitive monitoring of CRISPR-mediated genotoxicity in primary cells. Using this approach, we detect, map and characterize various types of induced-losses of heterozygosity and assess editing-associated chromosomal instability. Importantly, palbociclib prevents the appearance of such genomic rearrangements in hematopoietic stem cells without impairing cell fate or graft capability. Conversely, short-term risk is significantly increased with DNA-PKcs inhibitor AZD7648. Fortunately, targeting HBG1/2p, scSNP-DNA-seq reveals that ON-target genotoxic events are no longer detectable after long-term xenografts. This work demonstrates that scSNP-DNA-seq should be routinely implemented to monitor chromosomal rearrangements before and after CRISPR-edited cell infusions.

Indexed as

CRISPR-Cas SystemsGene EditingPiperazinesPyridinesSingle-Cell AnalysisAnimalsHematopoietic Stem CellsHumansMicePolymorphism, Single NucleotidepalbociclibPiperazinesPyridines

Identifiers

PMID41519897
PMCPMC12881610

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.