Evidence map›Paper›PMID 37344626›Full record

ReviewOncogene2023

Epigenetic regulation of hybrid epithelial-mesenchymal cell states in cancer.

Reilly A Sample, Marina F Nogueira, Robi D Mitra, Sidharth V Puram

Open access · greenAbstract readReview
In one paragraph

Review in Oncogene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
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  9. Review
  10. Article
  11. Epigenetic regulation of EZH2 by ncRNAs: mechanisms and oncogenic implications.Naunyn-Schmiedeberg's archives of pharmacology · 2026
    Review
  12. Article
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  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Epigenetic regulation of cancer stemness.Signal transduction and targeted therapy · 2025
    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

4 authors at 1 institution in 1 country.

Reilly A SampleDepartment of Genetics, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0001-5830-5083
Marina F NogueiraDepartment of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
Robi D MitraDepartment of Genetics, Washington University School of Medicine, St. Louis, MO, USA. rmitra@wustl.edu.
Sidharth V PuramDepartment of Genetics, Washington University School of Medicine, St. Louis, MO, USA. sidpuram@wustl.edu.ORCID 0000-0003-3543-889X
Washington University in St. Louis · US

Funding

INSTITUTIONAL TRAINING GRANT IN GENOMIC SCIENCET32HG000045 · NHGRI · WASHINGTON UNIVERSITY · PI MICHAEL R BRENT, Barak A Cohen · 1997 to 2026
$8.4M
Molecular recording to predict cell fate decisions and animal behaviorRF1MH126723 · NIMH · WASHINGTON UNIVERSITY · PI DOUGHERTY, JOSEPH D, MITRA, ROBI D · 2021 to 2021
$3.7M
PARALLEL ANALYSIS OF TRANSCRIPTION AND PROTEIN-DNAINTERACTIONS IN SINGLE CNS CELLSRF1MH117070 · NIMH · WASHINGTON UNIVERSITY · PI DOUGHERTY, JOSEPH D, MITRA, ROBI D · 2018 to 2020
$3.2M
Dissecting hybrid epithelial-mesenchymal states in head and neck cancerR01DE032371 · NIDCR · WASHINGTON UNIVERSITY · PI Sidharth Venkata Puram · 2023 to 2026
$1.6M
COOPERATIVITY AND COLLECTIVE BINDING IN TRANSCRIPTION FACTOR-DNA INTERACTIONSR01GM123203 · NIGMS · WASHINGTON UNIVERSITY · PI MITRA, ROBI D · 2018 to 2021
$1.6M
Understanding programs of invasion and metastasis in head and neck cancerK08CA237732 · NCI · WASHINGTON UNIVERSITY · PI PURAM, SIDHARTH VENKATA · 2019 to 2023
$984k
An inducible molecular memory system to unravel the mechanisms of drug resistance in head and neck cancerR21DE031366 · NIDCR · WASHINGTON UNIVERSITY · PI MITRA, ROBI D, PURAM, SIDHARTH VENKATA · 2022 to 2023
$433k
RNA modification and the regulation of partial EMT in head and neck cancerR21DE031072 · NIDCR · WASHINGTON UNIVERSITY · PI PURAM, SIDHARTH VENKATA · 2021 to 2022
$433k
NCI NIH HHS K08 CA237732NHGRI NIH HHS T32 HG000045NIDCR NIH HHS R01 DE032371NIDCR NIH HHS R21 DE031072NIDCR NIH HHS R21 DE031366NIGMS NIH HHS R01 GM123203NIMH NIH HHS RF1 MH117070NIMH NIH HHS RF1 MH126723
6 · The paper itself

Abstract

Epithelial-to-mesenchymal transition (EMT) is a process by which cells lose their epithelial characteristics and gain mesenchymal phenotypes. In cancer, EMT is thought to drive tumor invasion and metastasis. Recent efforts to understand EMT biology have uncovered that cells undergoing EMT attain a spectrum of intermediate "hybrid E/M" states, which exist along an epithelial-mesenchymal continuum. Here, we summarize recent studies characterizing the epigenetic drivers of hybrid E/M states. We focus on the histone-modification writers, erasers, and readers that assist or oppose the canonical hybrid E/M transcription factors that modulate hybrid E/M state transitions. We also examine the role of chromatin remodelers and DNA methylation in hybrid E/M states. Finally, we highlight the challenges of targeting hybrid E/M pharmacologically, and we propose future directions that might reveal the specific and targetable mechanisms by which hybrid E/M drives metastasis in patients.

Indexed as

Epigenesis, GeneticNeoplasmsEpithelial CellsEpithelial-Mesenchymal TransitionHumansPhenotypeTranscription FactorsTranscription Factors

Identifiers

PMID37344626
PMCPMC10578205
OpenAlexW4381480939

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.