Evidence map›Paper›PMID 31492885›Full record

ArticleNature communications2019

ARID1A promotes genomic stability through protecting telomere cohesion.

Bo Zhao, Jianhuang Lin, Lijie Rong, Shuai Wu, Zhong Deng, Nail Fatkhutdinov, Joseph Zundell, Takeshi Fukumoto, Qin Liu, Andrew Kossenkov and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 64 citations in OpenAlex.

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  8. Diagnostics (Basel, Switzerland) · 2025
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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

17 authors at 3 institutions in 1 country.

Bo ZhaoGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA.
Jianhuang LinGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA.ORCID http://orcid.org/0000-0002-0035-0938
Lijie RongDepartment of Pharmacology, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Shuai WuGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA.
Zhong DengGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA.
Nail FatkhutdinovGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA.
Joseph ZundellGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA.
Takeshi FukumotoGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA.
Qin LiuMolecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, PA, 19104, USA.ORCID http://orcid.org/0000-0001-9964-580X
Andrew KossenkovCenter for Systems and Computational Biology, The Wistar Institute, Philadelphia, PA, 19104, USA.
Stephanie JeanHelen F. Graham Cancer Center & Research Institute, Newark, DE, 19713, USA.
Mark G CadungogHelen F. Graham Cancer Center & Research Institute, Newark, DE, 19713, USA.
Mark E BorowskyHelen F. Graham Cancer Center & Research Institute, Newark, DE, 19713, USA.
Ronny DrapkinDepartment of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Paul M LiebermanGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA.
Cory T Abate-ShenDepartment of Pharmacology, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Rugang ZhangGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA, 19104, USA. rzhang@wistar.org.ORCID http://orcid.org/0000-0002-7255-2360
The Wistar Institute · USColumbia University Irving Medical Center · USUniversity of Pennsylvania · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
STRUCTURAL BASIS FOR EPIGENETICS IN AGING AND LONGEVITYP01AG031862 · NIA · WISTAR INSTITUTE · PI GARCIA, BENJAMIN A · 2008 to 2022
$28.3M
SPORE in Ovarian CancerP50CA228991 · NCI · JOHNS HOPKINS UNIVERSITY · PI Tian-Li Wang · 2018 to 2026
$20.5M
Project 3: Modeling tumor evolution and drug response in bladder cancer organoidsP01CA221757 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHEN, MICHAEL M. · 2018 to 2022
$8.6M
Preclinical analyses of advanced prostate cancer in genetically-engineered miceR01CA173481 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Cory Abate-Shen · 2013 to 2026
$6.1M
Role of TERRA in Telomere Maintenance and Telomere Stress ResponseR01CA140652 · NCI · WISTAR INSTITUTE · PI LIEBERMAN, PAUL M. · 2010 to 2025
$6.0M
Molecular mechanisms of prostate cancer metastasisR01CA183929 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ABATE-SHEN, CORY · 2015 to 2025
$4.1M
Mechanistic basis and therapeutic strategies for ARID1A mutation in ovarian cancerR01CA202919 · NCI · WISTAR INSTITUTE · PI Xi Chen, Rugang Zhang · 2016 to 2026
$4.1M
Role of BRCA1 Pathway in Regulating Oncogene-Induced SenescenceR01CA160331 · NCI · WISTAR INSTITUTE · PI ZHANG, RUGANG · 2012 to 2021
$4.0M
Targeting EZH2 in CARM1-expressing epithelial ovarian cancerR01CA163377 · NCI · WISTAR INSTITUTE · PI ZHANG, RUGANG · 2012 to 2021
$3.7M
Synthetic lethality based combination approaches to ARID1A mutation in ovarian cancerR01CA239128 · NCI · WISTAR INSTITUTE · PI ZHANG, RUGANG · 2019 to 2024
$2.5M
Advancing Cancer Research through Comprehensive Proteomics and Metabolomics AnalysesR50CA221838 · NCI · WISTAR INSTITUTE · PI Hsin-Yao Tang · 2017 to 2026
$2.1M
NCI NIH HHS P01 CA221757NCI NIH HHS P30 CA010815NCI NIH HHS P50 CA228991NCI NIH HHS R01 CA140652NCI NIH HHS R01 CA160331NCI NIH HHS R01 CA163377NCI NIH HHS R01 CA173481NCI NIH HHS R01 CA183929NCI NIH HHS R01 CA202919NCI NIH HHS R01 CA239128NCI NIH HHS R50 CA211199NCI NIH HHS R50 CA221838NIA NIH HHS P01 AG031862
6 · The paper itself

Abstract

ARID1A inactivation causes mitotic defects. Paradoxically, cancers with high ARID1A mutation rates typically lack copy number alterations (CNAs). Here, we show that ARID1A inactivation causes defects in telomere cohesion, which selectively eliminates gross chromosome aberrations during mitosis. ARID1A promotes the expression of cohesin subunit STAG1 that is specifically required for telomere cohesion. ARID1A inactivation causes telomere damage that can be rescued by STAG1 expression. Colony formation capability of single cells in G

Indexed as

Genomic InstabilityMutationAnimalsApoptosisCell Cycle ProteinsCell LineCell Line, TumorChromosomal Proteins, Non-HistoneCohesinsDNA-Binding ProteinsDNA Copy Number VariationsFemaleHumansMice, Inbred NODMice, KnockoutMice, SCIDARID1A protein, humanCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsDNA-Binding ProteinsNuclear ProteinsTranscription Factors

Identifiers

PMID31492885
PMCPMC6731242
OpenAlexW2971968397

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.