Evidence map›Paper›PMID 40170512›Full record

ArticleMolecular oncology2025

Multidimensional OMICs reveal ARID1A orchestrated control of DNA damage, splicing, and cell cycle in normal-like and malignant urothelial cells.

Rebecca M Schlösser, Florian Krumbach, Eyleen Corrales, Geoffroy Andrieux, Christian Preisinger, Franziska Liss, Alexandra Golzmann, Melanie Boerries, Kerstin Becker, Ruth Knüchel and 2 more

Abstract read
In one paragraph

Article in Molecular oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Rebecca M SchlösserInstitute of Pathology, RWTH Aachen University Hospital, Aachen, Germany.ORCID 0009-0007-9816-0342
Florian KrumbachInstitute of Pathology, RWTH Aachen University Hospital, Aachen, Germany.
Eyleen CorralesInstitute of Medical Bioinformatics and Systems Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Germany.ORCID 0000-0002-4767-1640
Geoffroy AndrieuxInstitute of Medical Bioinformatics and Systems Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Germany.ORCID 0000-0002-5389-9481
Christian PreisingerProteomics Facility, Interdisciplinary Centre for Clinical Research (IZKF), Medical School, RWTH Aachen University, Aachen, Germany.ORCID 0000-0003-1233-9063
Franziska LissInstitute of Pathology, RWTH Aachen University Hospital, Aachen, Germany.
Alexandra GolzmannInstitute of Biochemistry and Molecular Biology, Faculty of Medicine, RWTH Aachen University, Aachen, Germany.
Melanie BoerriesInstitute of Medical Bioinformatics and Systems Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Germany.ORCID 0000-0002-3670-0602
Kerstin BeckerCologne Center for Genomics (CCG), Medical Faculty, University of Cologne, Germany.ORCID 0009-0009-7897-7181
Ruth KnüchelInstitute of Pathology, RWTH Aachen University Hospital, Aachen, Germany.ORCID 0000-0002-4987-701X
Stefan GarczykInstitute of Pathology, RWTH Aachen University Hospital, Aachen, Germany.
Bernhard LüscherInstitute of Biochemistry and Molecular Biology, Faculty of Medicine, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-9622-8709

Funding

Bundesministerium für Bildung und Forschung EkoEstMed-FKZ 01ZZ2015Bundesministerium für Bildung und Forschung PM4Onco-FKZ 01ZZ2322ACRC1160 256073931-Z02CRC1453 431984000-S1CRC1479 441891347-S1CRC/TRR167 259373024-Z01Deutsche Forschungsgemeinschaft 432235170FOR5476 493802833-P7TRR359 491676693-Z01
6 · The paper itself

Abstract

Epigenetic regulators, such as the SWI/SNF complex, with important roles in tissue development and homeostasis, are frequently mutated in cancer. ARID1A, a subunit of the SWI/SNF complex, is mutated in approximately 20% of all bladder tumors; however, the consequences of this remain poorly understood. Finding truncations to be the most common mutation, we generated loss- and gain-of-function models to conduct RNA-Seq, interactome analyses, Omni-ATAC-Seq, and functional studies to characterize ARID1A-affected pathways potentially suitable for the treatment of ARID1A-deficient bladder cancers. We observed decreased cell proliferation and deregulation of stress-regulated pathways, including DNA repair, in ARID1A-deficient cells. Furthermore, ARID1A was linked to alternative splicing and translational regulation on RNA and interactome levels. ARID1A deficiency drastically reduced the accessibility of chromatin, especially around introns and distal enhancers, in a functional enrichment analysis. Less accessible chromatin areas were mapped to pathways such as cell proliferation and DNA damage response. Indeed, the G2/M checkpoint appeared impaired after DNA damage in ARID1A-deficient cells. Together, our data highlight the broad impact of ARID1A loss and the possibility of targeting proliferative and DNA repair pathways for treatment.

Indexed as

Cell CycleDNA-Binding ProteinsDNA DamageRNA SplicingTranscription FactorsUrinary Bladder NeoplasmsUrotheliumAlternative SplicingCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansARID1A protein, humanDNA-Binding ProteinsTranscription FactorsARID1AATAC‐Seqbladder cancerDNA‐damage checkpointsRNA‐SeqSWI/SNF

Identifiers

PMID40170512
PMCPMC12688176

What OpenQuestion holds

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Registered trials

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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.