Evidence map›Paper›PMID 21499305›Full record

ArticleOncogene2011

MEK-ERK pathway regulates EZH2 overexpression in association with aggressive breast cancer subtypes.

S Fujii, K Tokita, N Wada, K Ito, C Yamauchi, Y Ito, A Ochiai

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing 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

74 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
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  10. Review
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  12. Article
  13. The roles of EZH2 in cancer and its inhibitors.Medical oncology (Northwood, London, England) · 2023
    Review
  14. circEZH2Cancer science · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

14 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

7 authors at 3 institutions in 2 countries.

S FujiiPathology Division, Research Center for Innovative Oncology, National Cancer Center at Kashiwa, Chiba, Japan.
K Tokita
N Wada
K Ito
C Yamauchi
Y Ito
A Ochiai
National Cancer Center Hospital East · JPNagasaki University · JPNational University Cancer Institute, Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EZH2 overexpression occurs in various malignancies and is associated with a poor outcome. We have so far demonstrated that EZH2 downregulates the important genes such as E-cadherin and RUNX3 by increasing histone H3K27 trimethylation. However, the mechanism of EZH2 overexpression in various cancer cells remains unclear. In this study we carried out a promoter analysis of the EZH2 gene and investigated whether a survival signal that is upregulated in cancer cells is related to overexpression at the transcription level. We also explored the clinical relevance of the signaling pathway that leads to EZH2 overexpression in breast cancer and demonstrated that MEK-ERK1/2-Elk-1 pathway leads to EZH2 overexpression. The triple-negative and ERBB2-overexpressing subtypes of breast cancer are known to contain more rapidly proliferating breast cancer cells. The signaling pathway connected to EZH2 overexpression was associated with both aggressive subtypes of breast cancer. We show the significance that overexpression of histone modifier protein EZH2 in cancer cells and our study could pave the way for EZH2 inhibition to become an efficient treatment for more aggressive breast cancers.

Indexed as

Breast NeoplasmsCell Line, TumorChromatin ImmunoprecipitationDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinErb-b2 Receptor Tyrosine Kinasesets-Domain Protein Elk-1Extracellular Signal-Regulated MAP KinasesFemaleHumansMAP Kinase Kinase KinasesPolycomb Repressive Complex 2Polymerase Chain ReactionPromoter Regions, GeneticRNA InterferenceRNA, Small InterferingDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasesets-Domain Protein Elk-1Extracellular Signal-Regulated MAP KinasesEZH2 protein, humanMAP Kinase Kinase KinasesPolycomb Repressive Complex 2RNA, Small InterferingTranscription Factors

Identifiers

PMID21499305
OpenAlexW2067155951

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.