Evidence map›Paper›PMID 26617740›Full record

ArticleInternational journal of clinical and experimental pathology2015

Overexpression of histone demethylase JMJD5 promotes metastasis and indicates a poor prognosis in breast cancer.

Zhihua Zhao, Chuntao Sun, Fengqi Li, Jiankui Han, Xanjun Li, Zhenguo Song

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. JMJD5: a multifunctional regulator in development, homeostasis, and cancer.Frontiers in cell and developmental biology · 2026
    Review
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  17. The small members of the JMJD protein family: Enzymatic jewels or jinxes?Biochimica et biophysica acta. Reviews on cancer · 2019
    Review
  18. Article
  19. JMJD5 is a human arginyl C-3 hydroxylase.Nature communications · 2018
    Article
  20. Miz1 Controls Schwann Cell Proliferation via H3K36The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    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

6 authors at 2 institutions in 1 country.

Zhihua ZhaoDepartment of Nuclear Medicine, Qilu Hospital, Shandong University Wenhua Xi Road, Jinan 250012, Shandong Province, China ; Department of Nuclear Medicine, Weifang People's Hospital Weifang 261000, Shandong Province, China.
Chuntao SunDepartment of Interventional Radiology, Weifang Peoples Hospital Weifang 261000, Shandong Province, China.
Fengqi LiDepartment of Nuclear Medicine, Weifang People's Hospital Weifang 261000, Shandong Province, China.
Jiankui HanDepartment of Nuclear Medicine, Qilu Hospital, Shandong University Wenhua Xi Road, Jinan 250012, Shandong Province, China.
Xanjun LiDepartment of Nuclear Medicine, Weifang People's Hospital Weifang 261000, Shandong Province, China.
Zhenguo SongDepartment of Nuclear Medicine, Weifang People's Hospital Weifang 261000, Shandong Province, China.
Weifang People's Hospital · CNQilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we showed the expression of JMJD5 was increased in breast cancer tissues and breast adenocarcinoma cell lines MCF-7 as well as triple negative breast cancer cell lines MDA-MB-231 compared with paired adjacent normal mammary tissues and normal mammary epithelial cell lines MCF-10A. The higher expression of JMJD5 was significantly corresponded with clinical stage, histological grade and lymph node metastasis. Overexpression of JMJD5 promoted cell invasion and induce EMT, while JMJD5 siRNA inhibits MDA-MB-231 cells invasion in vitro. Moreover, qChIP analysis revealed the Snail family proteins Snai1 was the direct target of JMJD5 in breast cancer cells. Luciferase reporter assays suggested that the overexpression of JMJD5 resulted in the activation of Snail1 promoter-driven luciferase reporter. The changes in the level of RNA and protein implied that the activation of Snail was the important mechanisms by which JMJD5 triggers metastasis. We also detected the higher expression of JMJD5 protein was an independent unfavorable biomarker for worse overall survival in breast cancer patients. Therefore, our results identified an important role for JMJD5 in breast cancer through the regulation of snail1.

Indexed as

AdenocarcinomaAdultAgedBreast NeoplasmsCell Line, TumorFemaleHistone DemethylasesHumansLymphatic MetastasisMiddle AgedNeoplasm InvasivenessPrognosisPromoter Regions, GeneticSnail Family Transcription FactorsTranscription FactorsTriple Negative Breast NeoplasmsHistone DemethylasesKDM8 protein, humanSNAI1 protein, humanSnail Family Transcription FactorsTranscription Factorsbiomarkerbreast cancerJMJD5metastasissnail

Identifiers

PMID26617740
PMCPMC4637555
OpenAlexW2187790753

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.