Evidence map›Paper›PMID 33057161›Full record

ArticleActa pharmacologica Sinica2021

EZH2 regulates expression of FOXC1 by mediating H3K27me3 in breast cancers.

Xiang-Jin Zheng, Wan Li, Jie Yi, Jin-Yi Liu, Li-Wen Ren, Xiao-Ming Zhu, Shi-Wei Liu, Jin-Hua Wang, Guan-Hua Du

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. The Role of the Fox Gene in Breast Cancer Progression.International journal of molecular sciences · 2025
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

9 authors at 3 institutions in 2 countries.

Xiang-Jin Zheng *The State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Wan Li *The State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Jie YiDepartment of Clinical Laboratory, Peking Union Medical College Hospital, Beijing, 100032, China.
Jin-Yi LiuThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Li-Wen RenThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Xiao-Ming ZhuState Key Laboratory of Quality Research in Chinese Medicine, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau, China.
Shi-Wei LiuDepartment of Endocrinology, Shanxi DAYI Hospital, Shanxi Medical University, Taiyuan, 030002, China.
Jin-Hua WangThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China. wjh@imm.ac.cn.
Guan-Hua DuThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China. dugh@imm.ac.cn.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNMacau University of Science and Technology · MOShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is characterized by low expression of human epidermal growth factor receptor-2 (HER2), estrogen receptor (ER), and progesterone receptor (PR), which is the most aggressive subtype with poor outcome among breast cancers. The underlying mechanisms of TNBC remain unclear and there is a lack of biomarkers. In this study we conducted an in silico assay and found that FOXC1 was highly expressed in ER

Indexed as

Biomarkers, TumorCell Line, TumorDrug Resistance, NeoplasmEnhancer of Zeste Homolog 2 ProteinForkhead Transcription FactorsHistonesHumansMethylationTriple Negative Breast NeoplasmsBiomarkers, TumorEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanForkhead Transcription FactorsFOXC1 protein, humanHistonesdrug resistanceEZH2FOXC1H3K27me3TNBC

Identifiers

PMID33057161
PMCPMC8209002
OpenAlexW3092749004

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.