Evidence map›Paper›PMID 34429326›Full record

ArticleCancer research2021

mTORC1 Promotes ARID1A Degradation and Oncogenic Chromatin Remodeling in Hepatocellular Carcinoma.

Shanshan Zhang, Yu-Feng Zhou, Jian Cao, Stephen K Burley, Hui-Yun Wang, X F Steven Zheng

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 38 citations in OpenAlex.

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  13. ARID1A and Its Impact Across the Hallmarks of Cancer.International journal of molecular sciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Shanshan ZhangRutgers Cancer Institute of New Jersey, Rutgers, The State University of New Jersey, New Brunswick, New Jersey.
Yu-Feng ZhouState Key Laboratory of Oncology in South China and Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Jian CaoRutgers Cancer Institute of New Jersey, Rutgers, The State University of New Jersey, New Brunswick, New Jersey.ORCID 0000-0003-3424-6802
Stephen K BurleyRutgers Cancer Institute of New Jersey, Rutgers, The State University of New Jersey, New Brunswick, New Jersey.ORCID 0000-0002-2487-9713
Hui-Yun WangRutgers Cancer Institute of New Jersey, Rutgers, The State University of New Jersey, New Brunswick, New Jersey. zhengst@cinj.rutgers.edu wanghy@sysucc.org.cn.ORCID 0000-0001-6728-4376
X F Steven ZhengRutgers Cancer Institute of New Jersey, Rutgers, The State University of New Jersey, New Brunswick, New Jersey. zhengst@cinj.rutgers.edu wanghy@sysucc.org.cn.
Rutgers, The State University of New Jersey · USSun Yat-sen University · CN

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
PDB MANAGEMENT BY THE RESEARCH COLLABORATORY FOR STRUCTURAL BIOINFORMATICSR01GM133198 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI BURLEY, STEPHEN K · 2019 to 2023
$19.3M
Growth Control and Anti-Cancer MechanismsR01CA123391 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI ZHENG, STEVEN · 2007 to 2016
$2.9M
Oncogenic Chromatin Remodeling and Anticancer MechanismsR01CA280177 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI STEVEN ZHENG · 2023 to 2026
$1.8M
Metabolic Control and Anticancer MechanismR01CA260006 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI STEVEN ZHENG · 2021 to 2026
$1.7M
Amino Acids-Rab1A Nutrient Signaling in the Regulation of Glucose HomeostasisR01DK124897 · NIDDK · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI ZHENG, STEVEN · 2020 to 2023
$1.5M
NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA123391NCI NIH HHS R01 CA260006NCI NIH HHS R01 CA280177NIDDK NIH HHS R01 DK124897NIGMS NIH HHS R01 GM133198
6 · The paper itself

Abstract

The SWI/SNF chromatin remodeling complexes control accessibility of chromatin to transcriptional and coregulatory machineries. Chromatin remodeling plays important roles in normal physiology and diseases, particularly cancer. The ARID1A-containing SWI/SNF complex is commonly mutated and thought to be a key tumor suppressor in hepatocellular carcinoma (HCC), but its regulation in response to oncogenic signals remains poorly understood. mTOR is a conserved central controller of cell growth and an oncogenic driver of HCC. Remarkably, cancer mutations in mTOR and SWI/SNF complex are mutually exclusive in human HCC tumors, suggesting that they share a common oncogenic function. Here, we report that mTOR complex 1 (mTORC1) interact with ARID1A and regulates ubiquitination and proteasomal degradation of ARID1A protein. The mTORC1-ARID1A axis promoted oncogenic chromatin remodeling and YAP-dependent transcription, thereby enhancing liver cancer cell growth

Indexed as

Chromatin Assembly and DisassemblyGene Expression Regulation, NeoplasticAnimalsApoptosisBiomarkers, TumorCarcinoma, HepatocellularCell Cycle ProteinsCell ProliferationDNA-Binding ProteinsHumansLiver NeoplasmsMaleMechanistic Target of Rapamycin Complex 1MiceMutationPrognosisARID1A protein, humanBiomarkers, TumorCell Cycle ProteinsDNA-Binding ProteinsMechanistic Target of Rapamycin Complex 1MTOR protein, humanTOR Serine-Threonine KinasesTranscription FactorsYY1AP1 protein, human

Identifiers

PMID34429326
PMCPMC8595749
OpenAlexW3194506990

What OpenQuestion holds

Textmetadata
LicenceTDM
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.