Evidence map›Paper›PMID 33158812›Full record

ArticleCancer research2021

Loss of ARID1A Promotes Epithelial-Mesenchymal Transition and Sensitizes Pancreatic Tumors to Proteotoxic Stress.

Hideo Tomihara, Federica Carbone, Luigi Perelli, Justin K Huang, Melinda Soeung, Johnathon L Rose, Frederick S Robinson, Yonathan Lissanu Deribe, Ningping Feng, Mitsunobu Takeda and 12 more

Abstract 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 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Molecular interplay of ARID1A in gastrointestinal cancers.Medical oncology (Northwood, London, England) · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. ARID1A and Its Impact Across the Hallmarks of Cancer.International journal of molecular sciences · 2025
    Review
  13. Article
  14. KRASMolecular oncology · 2025
    Article
  15. Article
  16. Article
  17. Cancers · 2024
    Review
  18. Article
  19. Review
  20. Review
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

22 authors.

Hideo Tomihara *Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID https://orcid.org/0000-0003-4392-1187
Federica Carbone *Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID https://orcid.org/0000-0001-8697-0304
Luigi Perelli *Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Justin K HuangTherapeutics Discovery Division, TRACTION Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID https://orcid.org/0000-0002-9150-8533
Melinda SoeungDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Johnathon L RoseDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Frederick S RobinsonTherapeutics Discovery Division, TRACTION Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID https://orcid.org/0000-0003-1188-0376
Yonathan Lissanu DeribeDepartment of Thoracic and Cardio Surgery-Research, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ningping FengTherapeutics Discovery Division, TRACTION Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID https://orcid.org/0000-0003-1917-9648
Mitsunobu TakedaDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Akira InoueDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Edoardo Del PoggettoDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Angela K DeemDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Anirban MaitraDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pavlos MsaouelDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Nizar M TannirDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Giulio F DraettaDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Andrea VialeDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Timothy P HeffernanTherapeutics Discovery Division, TRACTION Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Christopher A BristowTherapeutics Discovery Division, TRACTION Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Alessandro CarugoTherapeutics Discovery Division, TRACTION Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas. ggenovese@mdanderson.org ACarugo@mdanderson.org.ORCID https://orcid.org/0000-0001-5182-3320
Giannicola GenoveseDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas. ggenovese@mdanderson.org ACarugo@mdanderson.org.

Funding

The RAS and P13K Pathways in Pancreatic AdenocarcinomaP01CA117969 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DEPINHO, RONALD ANTHONY · 2006 to 2025
$41.7M
Investigation of the role of epithelial-mesenchymal plasticity in renal cell carcinomaR01CA258226 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GENOVESE, GIANNICOLA · 2021 to 2025
$2.9M
NCI NIH HHS P01 CA117969NCI NIH HHS R01 CA258226
6 · The paper itself

Abstract

Cellular dedifferentiation is a key mechanism driving cancer progression. Acquisition of mesenchymal features has been associated with drug resistance, poor prognosis, and disease relapse in many tumor types. Therefore, successful targeting of tumors harboring these characteristics is a priority in oncology practice. The SWItch/Sucrose non-fermentable (SWI/SNF) chromatin remodeling complex has also emerged as a critical player in tumor progression, leading to the identification of several SWI/SNF complex genes as potential disease biomarkers and targets of anticancer therapies. AT-rich interaction domain-containing protein 1A (ARID1A) is a component of SWI/SNF, and mutations in

Indexed as

Epithelial-Mesenchymal TransitionAnimalsAntineoplastic AgentsApoptosisBiomarkers, TumorCarcinoma, Pancreatic DuctalCell ProliferationDNA-Binding ProteinsFemaleGene Expression Regulation, NeoplasticHSP90 Heat-Shock ProteinsHumansIsoxazolesMiceMice, NudePancreatic Neoplasms5-(2,4-dihydroxy-5-isopropylphenyl)-4-(4-morpholin-4-ylmethylphenyl)isoxazole-3-carboxylic acid ethylamideAntineoplastic AgentsARID1A protein, humanBiomarkers, TumorDNA-Binding ProteinsHSP90 Heat-Shock ProteinsIsoxazolesResorcinolsTranscription Factors

Identifiers

PMID33158812
PMCPMC8728103

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.