Evidence map›Paper›PMID 24618703›Full record

ReviewCancer biology & therapy2014

The emerging roles of ARID1A in tumor suppression.

Ren-Chin Wu, Tian-Li Wang, Ie-Ming Shih

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer biology & therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 155 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed, 4 pooled it
8.8field-weighted citation impact, top 1% of its field
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

155 citing papers in PubMed, 4 syntheses or guidelines pooled it, 269 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Phase II Trial and Correlative Genomic Analysis of Everolimus Plus Bevacizumab in Advanced Non-Clear Cell Renal Cell Carcinoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2016
    Trial
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Molecular interplay of ARID1A in gastrointestinal cancers.Medical oncology (Northwood, London, England) · 2025
    Review
  15. Article
  16. Review
  17. Article
  18. ARID1A and Its Impact Across the Hallmarks of Cancer.International journal of molecular sciences · 2025
    Review
  19. Review
  20. Article

95 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Ren-Chin WuDepartment of Pathology and Pathobiology Graduate Program; Johns Hopkins University School of Medicine; Baltimore, MD USA; Department of Pathology; Chang Gung Memorial Hospital and Chang Gung University College of Medicine; Taoyuan, Taiwan.
Tian-Li WangDepartment of Pathology and Pathobiology Graduate Program; Johns Hopkins University School of Medicine; Baltimore, MD USA; Departments of Oncology and Gynecology and Obstetrics; Johns Hopkins University School of Medicine; Baltimore, MD USA.
Ie-Ming ShihDepartment of Pathology and Pathobiology Graduate Program; Johns Hopkins University School of Medicine; Baltimore, MD USA; Departments of Oncology and Gynecology and Obstetrics; Johns Hopkins University School of Medicine; Baltimore, MD USA.
Johns Hopkins Medicine · USUniversity of Baltimore · US

Funding

Characterizing Notch3 Signaling in Ovarian CancerR01CA148826 · NCI · JOHNS HOPKINS UNIVERSITY · PI WANG, TIAN-LI · 2011 to 2015
$1.7M
Tumor Suppressor Role of ARID1AR21CA165807 · NCI · JOHNS HOPKINS UNIVERSITY · PI SHIH, IE-MING · 2012 to 2013
$375k
NCI NIH HHS CA165807NCI NIH HHS R01 CA148826NCI NIH HHS R21 CA165807
6 · The paper itself

Abstract

ARID1A has emerged as a tumor suppressor gene, which is mutated in a broad spectrum of cancers, especially in those arising from ectopic or eutopic endometrium. As a subunit of SWI/SNF chromatin remodeler, ARID1A facilitates target-specific binding of SWI/SNF complexes to chromatin, thereby altering the accessibility of chromatin to a variety of nuclear factors. In human cancer, ARID1A possesses not only features of a gatekeeper, regulating cell cycle progression, but also features of a caretaker, preventing genomic instability. An increasing body of evidence suggests crosstalk between ARID1A and PI3K/Akt pathways, and between ARID1A and p53. In this review, we discuss the spectrum of ARID1A alterations in cancers, tumor suppression mechanisms of ARID1A, oncogenic pathways cooperating with ARID1A, and clinical implications of ARID1A mutation.

Indexed as

AnimalsCarcinogenesisDNA-Binding ProteinsGenes, Tumor SuppressorGenomic InstabilityHumansMutationMutation RateNeoplasmsNuclear ProteinsSignal TransductionTranscription FactorsARID1A protein, humanDNA-Binding ProteinsNuclear ProteinsTranscription FactorsARID1Achromatin remodeling complexclear cell carcinomaendometrial cancerendometrioid carcinomagastric cancerovarian cancerPI3KSWI/SNFtumor suppressor gene

Identifiers

PMID24618703
PMCPMC4049780
OpenAlexW2068275655

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.