Evidence map›Paper›PMID 40429787›Full record

ReviewInternational journal of molecular sciences2025

ARID1A and Its Impact Across the Hallmarks of Cancer.

Bridger Kearns, Andralyn McKell, Isaac Steveson, Peyton Worley, Braeden Barton, Jordan Bennett, DeLaney Anderson, Jacob Harris, James Christensen, Jared J Barrott

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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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.

Bridger KearnsDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.
Andralyn McKellDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.ORCID 0009-0009-6917-6438
Isaac StevesonDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.
Peyton WorleyDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.
Braeden BartonDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.
Jordan BennettDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.
DeLaney AndersonDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.
Jacob HarrisDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.
James ChristensenDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.
Jared J BarrottDepartment of Cell Biology & Physiology, Brigham Young University, Provo, UT 84602, USA.ORCID 0000-0001-6059-9009

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ARID1A, a subunit of the SWI/SNF chromatin remodeling complex, has emerged as a pivotal tumor suppressor altered in a broad range of human malignancies. Its frequent inactivation across diverse cancer types has revealed pleiotropic roles that intersect multiple Hallmarks of Cancer. In this review, we integrate current knowledge on how ARID1A loss influences cellular processes including proliferative signaling, resistance to cell death, genomic instability, metabolic reprogramming, immune evasion, and more. We discuss the context-specific consequences of ARID1A deficiency, its cooperation with other oncogenic events, and its implications for therapeutic vulnerability-particularly in the realm of synthetic lethality and immune modulation. By mapping ARID1A's functional impact onto the established hallmarks framework, we highlight its centrality in cancer biology and underscore opportunities for biomarker-driven strategies and targeted interventions. Understanding ARID1A's multifaceted roles offers a compelling lens through which to explore chromatin dysregulation in cancer and guide translational advances.

Indexed as

DNA-Binding ProteinsNeoplasmsTranscription FactorsAnimalsChromatin Assembly and DisassemblyGene Expression Regulation, NeoplasticGenomic InstabilityHumansSignal TransductionARID1A protein, humanDNA-Binding ProteinsTranscription FactorsARID1Adedifferentiationgenomic instabilityimmune evasionproliferationsynthetic lethality

Identifiers

PMID40429787
PMCPMC12111594

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.