Evidence map›Paper›PMID 26645717›Full record

ArticleCarcinogenesis2016

Elevated expression of JMJD6 is associated with oral carcinogenesis and maintains cancer stemness properties.

Chang-Ryul Lee, Sung Hee Lee, Nicole Kristina Rigas, Reuben H Kim, Mo K Kang, No-Hee Park, Ki-Hyuk Shin

Open access · greenAbstract read
In one paragraph

Article in Carcinogenesis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
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  11. JMJD family proteins in cancer and inflammation.Signal transduction and targeted therapy · 2022
    Review
  12. Article
  13. A specific JMJD6 inhibitor potently suppresses multiple types of cancers both in vitro and in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  14. Widespread hydroxylation of unstructured lysine-rich protein domains by JMJD6.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Review
  16. Article
  17. Article
  18. Epigenetic crosstalk between hypoxia and tumor driven by HIF regulation.Journal of experimental & clinical cancer research : CR · 2020
    Review
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  20. 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

7 authors at 1 institution in 1 country.

Chang-Ryul LeeThe Shapiro Family Laboratory of Viral Oncology and Aging Research , UCLA School of Dentistry , Los Angeles, CA 90095 , USA.
Sung Hee LeeThe Shapiro Family Laboratory of Viral Oncology and Aging Research , UCLA School of Dentistry , Los Angeles, CA 90095 , USA.
Nicole Kristina RigasThe Shapiro Family Laboratory of Viral Oncology and Aging Research , UCLA School of Dentistry , Los Angeles, CA 90095 , USA.
Reuben H KimThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA 90095, USA.
Mo K KangThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA 90095, USA.
No-Hee ParkThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA 90095, USA.
Ki-Hyuk ShinThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA 90095, USA.
Oklahoma State University Center for Health Sciences · US

Funding

Epigenetic Control of HPV-associated Oral CarcinogenesisR01DE023874 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KIM, REUBEN HAN-KYU, WANG, CUN-YU · 2013 to 2017
$2.3M
Molecular mechanisms of drug-induced ONJ and osteomucosal chronic woundsR01DE023348 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KIM, REUBEN HAN-KYU · 2013 to 2017
$1.9M
Effects of Antiretroviral Therapy on Telomerase Function in Human Oral EpitheliumR01DE018295 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KANG, MO K. · 2007 to 2011
$1.7M
NIDCR NIH HHS R01DE023348NIDCR NIH HHS R01 DE023874NIDCR NIH HHS R01DE18295
6 · The paper itself

Abstract

Cancer stem cells (CSCs) are defined as a small subpopulation of cancer cells within a tumor and responsible for initiation and maintenance of tumor growth. Thus, understanding of molecular regulators of CSCs is of paramount importance for the development of effective cancer therapies. Here, we identified jumonji domain-containing protein 6 (JMJD6) as a novel molecular regulator of oral CSCs. JMJD6 is highly expressed in CSC-enriched populations of human oral squamous cell carcinoma (OSCC) cell lines. Moreover, immunohistochemical staining revealed significantly high level of JMJD6 in OSCC tissues compared to normal human oral epithelia, suggesting that expression of JMJD6 positively correlates with oral carcinogenesis. Subsequent functional analysis showed that knockdown of endogenous JMJD6 in OSCC strongly suppressed self-renewal capacity, a key characteristic of CSCs, and anchorage-independent growth. Conversely, ectopic expression of JMJD6 enhanced CSC characteristics including self-renewal, ALDH1 activity, migration/invasion and drug resistance. Expression of CSC-related genes was also markedly affected by modulating JMJD6 expression. Mechanistically, JMJD6 induces interleukin 4 (IL4) transcription by binding to its promoter region. IL4 rescues self-renewal capacity in JMJD6- knocked down OSCC cells, suggesting the importance of JMJD6-IL4 axis in oral CSCs. Our studies identify JMJD6 as a molecular determinant of CSC phenotype, suggesting that inhibition of JMJD6 may offer an effective therapeutic modality against oral cancer.

Indexed as

Blotting, WesternCarcinogenesisCarcinoma, Squamous CellCell Line, TumorChromatin ImmunoprecipitationFlow CytometryGene Knockdown TechniquesHumansImmunohistochemistryJumonji Domain-Containing Histone DemethylasesMouth NeoplasmsNeoplastic Stem CellsReal-Time Polymerase Chain ReactionJMJD6 protein, humanJumonji Domain-Containing Histone Demethylases

Identifiers

PMID26645717
PMCPMC5006207
OpenAlexW2190059975

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.