Evidence map›Paper›PMID 33890484›Full record

ReviewEpigenomics2021

ARID1 proteins: from transcriptional and post-translational regulation to carcinogenesis and potential therapeutics.

Olena Odnokoz, Cindy Wavelet-Vermuse, Shelby L Hophan, Serdar Bulun, Yong Wan

Open access · greenAbstract readReview
In one paragraph

Review in Epigenomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. SMARCD1 and Its Functional Relevance in SWI/SNF and Cancer.International journal of molecular sciences · 2026
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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

5 authors at 1 institution in 1 country.

Olena OdnokozDepartment of Obstetrics & Gynecology & Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0001-6690-7869
Cindy Wavelet-VermuseDepartment of Obstetrics & Gynecology & Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Shelby L HophanDepartment of Obstetrics & Gynecology & Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Serdar BulunDepartment of Obstetrics & Gynecology & Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Yong WanDepartment of Obstetrics & Gynecology & Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0001-9358-9392
Northwestern University · US

Funding

Targeting posttranslational modifications of CD73 in TNBCsR01CA258857 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Yong Wan, Bin Zhang · 2021 to 2026
$3.2M
Targeting posttranslational modifications of B7-H4 in carcinogenesis and therapyR01CA258765 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Yong Wan · 2021 to 2026
$2.5M
Targeting Posttranslational Modifications in Breast CarcinogenesisR01CA250110 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WAN, YONG · 2020 to 2025
$2.3M
Interplay between ER and TGF-b in carcinogenesisR01CA202948 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WAN, YONG · 2016 to 2021
$1.4M
Targeting interplay between KLF4 and PRMT5 in carcinogenesisR01CA202963 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WAN, YONG · 2016 to 2020
$1.3M
NCI NIH HHS R01 CA202948NCI NIH HHS R01 CA202963NCI NIH HHS R01 CA250110NCI NIH HHS R01 CA258765NCI NIH HHS R01 CA258857
6 · The paper itself

Abstract

The ARID1 proteins are mutually exclusive subunits of the BRG1/BRM-associated factor (BAF) complexes that play an important role in chromatin remodeling and regulate many fundamental cell functions. The role of ARID1s is well defined as a tumor-suppressive. The cancer cells evolve different mechanisms to downregulate ARID1s and inactivate their functions. ARID1s are frequently mutated in human cancer. The recent findings of ARID1A/B downregulation at transcriptional and translational levels along with their low levels in human cancers indicate the significance of regulatory mechanisms of ARID1s in cancers. In this review, we present the current knowledge on the regulation and alterations of ARID1 protein expression in human cancers and indicate the importance of regulators of ARID1s as a prognostic marker and in potential therapeutic strategies.

Indexed as

DNA-Binding ProteinsTranscription FactorsAnimalsCarcinogenesisDrug Resistance, NeoplasmHumansNeoplasmsProtein Processing, Post-TranslationalTranscription, GeneticARID1A protein, humanDNA-Binding ProteinsTranscription FactorsARID1AARID1BBAFcancerchromatin remodelerspost-translational modificationSWI/SNFtranscriptional regulationtumorigenesis

Identifiers

PMID33890484
PMCPMC8738980
OpenAlexW3152711024

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.