Evidence map›Paper›PMID 30759030›Full record

ReviewExpert opinion on therapeutic targets2019

Biology and targeting of the Jumonji-domain histone demethylase family in childhood neoplasia: a preclinical overview.

Tyler S McCann, Lays M Sobral, Chelsea Self, Joseph Hsieh, Marybeth Sechler, Paul Jedlicka

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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.

Tyler S McCanna Department of Pathology , University of Colorado Denver, Anschutz Medical Campus , Aurora , CO , USA.
Lays M Sobrala Department of Pathology , University of Colorado Denver, Anschutz Medical Campus , Aurora , CO , USA.
Chelsea Selfb Department of Pediatrics , University of Colorado Denver, Anschutz Medical Campus , Aurora , CO , USA.
Joseph Hsiehc Medical Scientist Training Program , University of Colorado Denver, Anschutz Medical Campus , Aurora , CO , USA.
Marybeth Sechlera Department of Pathology , University of Colorado Denver, Anschutz Medical Campus , Aurora , CO , USA.
Paul Jedlickaa Department of Pathology , University of Colorado Denver, Anschutz Medical Campus , Aurora , CO , USA.
University of Colorado Anschutz Medical Campus · USUniversity of Colorado Denver · US

Funding

Medical Scientist Training ProgramT32GM008497 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI WILSON, CARA C. · 1993 to 2022
$15.2M
Training Program in Cancer BiologyT32CA190216 · NCI · UNIVERSITY OF COLORADO DENVER · PI Craig T. Jordan · 2016 to 2026
$3.5M
Mechanism of tumor promotion by the H3K9 histone demethylase KDM3A in Ewing Sarcoma.R01CA183874 · NCI · UNIVERSITY OF COLORADO DENVER · PI JEDLICKA, PAUL · 2015 to 2019
$1.8M
The histone demethylase KDM3A upregulates MCAM to promote Ewing Sarcoma metastasisF31CA203053 · NCI · UNIVERSITY OF COLORADO DENVER · PI LUPO, MARYBETH SECHLER · 2016 to 2017
$46k
NCI NIH HHS F31 CA203053NCI NIH HHS R01 CA183874NCI NIH HHS T32 CA190216NIGMS NIH HHS T32 GM008497
6 · The paper itself

Abstract

introductionEpigenetic mechanisms of gene regulatory control play fundamental roles in developmental morphogenesis, and, as more recently appreciated, are heavily implicated in the onset and progression of neoplastic disease, including cancer. Many epigenetic mechanisms are therapeutically targetable, providing additional incentive for understanding of their contribution to cancer and other types of neoplasia. Areas covered: The Jumonji-domain histone demethylase (JHDM) family exemplifies many of the above traits. This review summarizes the current state of knowledge of the functions and pharmacologic targeting of JHDMs in cancer and other neoplastic processes, with an emphasis on diseases affecting the pediatric population. Expert opinion: To date, the JHDM family has largely been studied in the context of normal development and adult cancers. In contrast, comparatively few studies have addressed JHDM biology in cancer and other neoplastic diseases of childhood, especially solid (non-hematopoietic) neoplasms. Encouragingly, the few available examples support important roles for JHDMs in pediatric neoplasia, as well as potential roles for JHDM pharmacologic inhibition in disease management. Further investigations of JHDMs in cancer and other types of neoplasia of childhood can be expected to both enlighten disease biology and inform new approaches to improve disease outcomes.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic AgentsChildEpigenesis, GeneticHumansJumonji Domain-Containing Histone DemethylasesNeoplasmsAntineoplastic AgentsJumonji Domain-Containing Histone DemethylasescancerdemethylaseepigeneticsJumonjineoplasiapediatric

Identifiers

PMID30759030
PMCPMC6509558
OpenAlexW2912977317

What OpenQuestion holds

Textmetadata
LicenceTDM
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.