Evidence map›Paper›PMID 40011561›Full record

ArticleNature communications2025

PBRM1 directs PBAF to pericentromeres and protects centromere integrity.

Karen A Lane, Alison Harrod, Lillian Wu, Theodoros I Roumeliotis, Hugang Feng, Shane Foo, Katheryn A G Begg, Federica Schiavoni, Noa Amin, Frank T Zenke and 3 more

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Total whole-arm chromosome losses predict malignancy in human cancer.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
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

13 authors.

Karen A Lane *Division of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.ORCID http://orcid.org/0000-0003-0560-1502
Alison Harrod *Division of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.ORCID http://orcid.org/0000-0002-3977-2791
Lillian WuDivision of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.ORCID http://orcid.org/0000-0003-3178-1770
Theodoros I RoumeliotisDivision of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.ORCID http://orcid.org/0000-0002-3354-5643
Hugang FengDivision of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.
Shane FooDivision of Radiotherapy and Imaging, The Institute of Cancer Research; London, London, UK.ORCID http://orcid.org/0000-0001-6295-7404
Katheryn A G BeggDivision of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.
Federica SchiavoniDivision of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.
Noa AminDivision of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.
Frank T ZenkeMerck KGaA, Biopharma R&D, Translational Innovation Platform Oncology, Darmstadt, Germany.
Alan A MelcherDivision of Radiotherapy and Imaging, The Institute of Cancer Research; London, London, UK.ORCID http://orcid.org/0000-0002-2042-3380
Jyoti S ChoudharyDivision of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK.ORCID http://orcid.org/0000-0003-0881-5477
Jessica A DownsDivision of Cell and Molecular Biology, The Institute of Cancer Research; London, London, UK. Jessica.Downs@icr.ac.uk.ORCID http://orcid.org/0000-0002-6600-849X

Funding

Cancer Research UK (CRUK) C7905/A25715RCUK | Medical Research Council (MRC) MR/W001276/1
6 · The paper itself

Abstract

The specialised structure of the centromere is critical for effective chromosome segregation, but its repetitive nature makes it vulnerable to rearrangements. Centromere fragility can drive tumorigenesis, but protective mechanisms preventing fragility are still not fully understood. The PBAF chromatin remodelling complex is frequently misregulated in cancer, but its role in cancer is incompletely characterized. Here, we identify PBAF as a protector of centromere and pericentromere structure with profound consequences for genome stability. A conserved feature of isogenic cell lines lacking PBRM1, a subunit of PBAF, is compromised centromere and pericentromere integrity. PBAF is present at these regions, and binding patterns of PBAF and H3K9 methylation change when PBRM1 is absent. PBRM1 loss creates a dependence on the spindle assembly checkpoint, which represents a therapeutic vulnerability. Importantly, we find that even in the absence of any perturbations, PBRM1 loss leads to centromere fragility, thus identifying a key player in centromere protection.

Indexed as

CentromereDNA-Binding ProteinsNuclear ProteinsTranscription FactorsCell Line, TumorChromatin Assembly and DisassemblyChromosome SegregationGenomic InstabilityHistonesHumansDNA-Binding ProteinsHistonesNuclear ProteinsPBRM1 protein, humanTranscription Factors

Identifiers

PMID40011561
PMCPMC11865495

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.