Evidence map›Paper›PMID 27764784›Full record

ArticleOncotarget2016

DNA methylation promotes paired box 2 expression via myeloid zinc finger 1 in endometrial cancer.

Nan Jia, Jieyu Wang, Qing Li, Xiang Tao, Kaikai Chang, Keqin Hua, Yinhua Yu, Kwong-Kwok Wong, Weiwei Feng

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Epigenetic, Genetic, and Functional Germline Alterations ofCurrent issues in molecular biology · 2026
    Review
  2. Article
  3. DNMT Enzymes and Their Impact on Cervical Cancer: A State-of-the-Art Review.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Hypermethylation-Mediated Silencing ofInternational journal of molecular sciences · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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.

Nan JiaDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Jieyu WangDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Qing LiDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Xiang TaoDepartment of Pathology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Kaikai ChangDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Keqin HuaDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Yinhua YuShanghai Key Laboratory of Female Reproductive Endocrine-Related Disease, Fudan University, Shanghai, China.
Kwong-Kwok WongDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Weiwei FengDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This work investigated the role of paired box 2 (PAX2) in endometrial cancer and its epigenetic regulation mechanism. Endometrial cancer tissues and cell lines exhibited increased PAX2 expression compared with hyperplasia, normal endometrium and endometrial epithelial cells. Knock-down of PAX2 resulted in reduced cell viability, invasion and migration, and PAX2 overexpression caused the opposite effects. Increased methylation of the PAX2 promoter was observed in both cancer tissues and cell lines and was positively correlated with PAX2 expression. After 5-Aza-CdR treatment, PAX2 mRNA and protein were down-regulated, and PAX2 methylation was decreased. Deletion analysis confirmed that a repressive transcriptional regulatory region of the PAX2 promoter coincided with the hypermethylated region identified in MassARRAY analysis. Binding sites of myeloid zinc finger 1 (MZF1) are predicted in the defined region. Knock-down of MZF1 up-regulated the transcriptional activity and protein level of PAX2 after 5-Aza-CdR treatment, which indicated that MZF1 may act as a repressive transcription factor when the PAX2 promoter is unmethylated. In conclusion, PAX2 is involved in the carcinogenesis of endometrial cancer by stimulating cell growth and promoting cell motility. The overexpression of PAX2 in endometrial cancer is regulated by promoter hypermethylation and the transcription factor MZF1.

Indexed as

Antimetabolites, AntineoplasticAzacitidineCell Line, TumorCell MovementCell SurvivalDecitabineDNA MethylationEndometrial NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansKruppel-Like Transcription FactorsPAX2 Transcription FactorPromoter Regions, GeneticRNA, Small InterferingUp-RegulationAntimetabolites, AntineoplasticAzacitidineDecitabineKruppel-Like Transcription FactorsMZF1 protein, humanPAX2 protein, humanPAX2 Transcription FactorRNA, Small InterferingDNA methylationendometrial cancerMassARRAYmyeloid zinc finger 1paired box 2

Identifiers

PMID27764784
PMCPMC5356698

What OpenQuestion holds

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Registered trials

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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.