Evidence map›Paper›PMID 29726819›Full record

ReviewMolecular cancer therapeutics2018

Histone Methyltransferase EZH2: A Therapeutic Target for Ovarian Cancer.

Bayley A Jones, Sooryanarayana Varambally, Rebecca C Arend

Open access · greenAbstract readReview
In one paragraph

Review in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
4.7field-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

70 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. The role of epigenetics in cancer: From pathways to the clinic.Journal of family medicine and primary care · 2025
    Review
  11. Chromatin Organization Governs Transcriptional Response and Plasticity of Cancer Stem Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  12. Article
  13. Article
  14. Review
  15. A framework for target discovery in rare cancers.bioRxiv : the preprint server for biology · 2024
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

10 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Bayley A JonesUniversity of Alabama at Birmingham School of Medicine, Birmingham, Alabama.
Sooryanarayana VaramballyDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama.
Rebecca C ArendDepartment of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, Alabama. rarend@uabmc.edu.
University of Alabama at Birmingham · US

Funding

Role of Transcriptional Corepressor CtBP1 in Prostate Cancer ProgressionR01CA154980 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VARAMBALLY, SOORYANARAYANA · 2012 to 2016
$1.5M
NCI NIH HHS L30 CA209715NCI NIH HHS R01 CA154980
6 · The paper itself

Abstract

Ovarian cancer is the fifth leading cause of cancer-related deaths in females in the United States. There were an estimated 22,440 new cases and 14,080 deaths due to ovarian cancer in 2017. Most patients present with advanced-stage disease, revealing the urgent need for new therapeutic strategies targeting pathways of tumorigenesis and chemotherapy resistance. While multiple genomic changes contribute to the progression of this aggressive disease, it has become increasingly evident that epigenetic events play a pivotal role in ovarian cancer development. One of the well-studied epigenetic modifiers, the histone methyltransferase EZH2, is a member of polycomb repressive complex 2 (PRC2) and is commonly involved in transcriptional repression. EZH2 is the enzymatic catalytic subunit of the PRC2 complex that can alter gene expression by trimethylating lysine 27 on histone 3 (H3K27). In ovarian cancer, EZH2 is commonly overexpressed and therefore potentially serves as an effective therapeutic target. Multiple small-molecule inhibitors are being developed to target EZH2, which are now in clinical trials. Thus, in this review, we highlight the progress made in EZH2-related research in ovarian cancer and discuss the potential utility of targeting EZH2 with available small-molecule inhibitors for ovarian cancer.

Indexed as

Gene Expression Regulation, NeoplasticEnhancer of Zeste Homolog 2 ProteinFemaleHistonesHumansLysineMethylationMolecular Targeted TherapyOvarian NeoplasmsSmall Molecule LibrariesEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHistonesLysineSmall Molecule Libraries

Identifiers

PMID29726819
PMCPMC5939583
OpenAlexW2790335078

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.