Evidence map›Paper›PMID 35239138›Full record

ReviewClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2022

Emerging roles of JMJD3 in cancer.

Maryam Farzaneh, Zeinab Kuchaki, Fatima Rashid Sheykhahmad, Seyed Mohammadmahdi Meybodi, Yusef Abbasi, Effat Gholami, Farhoodeh Ghaedrahmati, Omid Anbiyaee

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Epigenetic (De)regulation in Prostate Cancer.Cancer treatment and research · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 8 institutions in 2 countries.

Maryam FarzanehFertility, Infertility and Perinatology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran. Maryamfarzaneh2013@yahoo.com.ORCID http://orcid.org/0000-0001-6239-8745
Zeinab KuchakiDepartment of Nursing, Faculty of Nursing and Midwifery, Shahed University, Tehran, Iran.
Fatima Rashid SheykhahmadDepartment of Internal Medicine, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran. fatima.rashid2014@yahoo.com.
Seyed Mohammadmahdi MeybodiDepartment of Veterinary Medicine, Tabriz Branch, Islamic Azad University, Tabriz, Iran.
Yusef AbbasiDepartment of Anatomy, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.
Effat GholamiSection of Zoology and Biological Anthropology, Department of Evolutionary Biology, Ecology and Environmental Sciences, Faculty of Biology, University of Barcelona (UB), Barcelona, Spain.
Farhoodeh GhaedrahmatiDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Omid AnbiyaeeCardiovascular Research Center, Nemazi Hospital, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Ahvaz Jundishapur University of Medical Sciences · IRArak University of Medical Sciences · IRArdabil University of Medical Sciences · IRIsfahan University of Medical Sciences · IRIslamic Azad University of Tabriz · IRShahed University · IRShiraz University of Medical Sciences · IRUniversitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histone lysine methylation plays a key role in gene activation and repression. The trimethylation of histone H3 on lysine-27 (H3K27me3) is a critical epigenetic event that is controlled by Jumonji domain-containing protein-3 (JMJD3). JMJD3 is a histone demethylase that specifically removes methyl groups. Previous studies have suggested that JMJD3 has a dual role in cancer cells. JMJD3 stimulates the expression of proliferative-related genes and increases tumor cell growth, propagation, and migration in various cancers, including neural, prostate, ovary, skin, esophagus, leukemia, hepatic, head and neck, renal, lymphoma, and lung. In contrast, JMJD3 can suppress the propagation of tumor cells, and enhance their apoptosis in colorectal, breast, and pancreatic cancers. In this review, we summarized the recent advances of JMJD3 function in cancer cells.

Indexed as

LysineNeoplasmsApoptosisFemaleHistonesHumansJumonji Domain-Containing Histone DemethylasesMaleMethylationHistonesJumonji Domain-Containing Histone DemethylasesLysineCancerEpigenomeInvasionJMJD3Metastasis

Identifiers

PMID35239138
OpenAlexW4214841001

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.