Evidence map›Paper›PMID 33174020›Full record

ArticleInternational journal of oncology2020

Cooperation between ETS transcription factor ETV1 and histone demethylase JMJD1A in colorectal cancer.

Sangphil Oh, Hoogeun Song, Willard M Freeman, Sook Shin, Ralf Janknecht

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

18 citing papers in PubMed, 19 citations in OpenAlex.

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  17. Sumoylation of transcription factor ETV1 modulates its oncogenic potential in prostate cancer.International journal of clinical and experimental pathology · 2021
    Article
  18. 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

5 authors at 2 institutions in 1 country.

Sangphil Oh *Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Hoogeun Song *Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Willard M FreemanStephenson Cancer Center, Oklahoma City, OK 73104, USA.
Sook ShinDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Ralf JanknechtDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
University of Oklahoma Health Sciences Center · USOU Health Stephenson Cancer Center

Funding

Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Wade Williams · 2018 to 2026
$27.1M
TUMOR RESISTANCE MECHANISMS TO ANTI-VEGF THERAPY IN PROSTATE CANCER (Sukyung Woo)P20GM103639 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DHANASEKARAN, DANNY N. · 2012 to 2022
$21.3M
ETV1 and JMJD2 Demethylases in Prostate CancerR01CA154745 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI JANKNECHT, RALF · 2011 to 2015
$1.5M
Regulation of KDM4A by Lysine MethylationR03CA223615 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI JANKNECHT, RALF · 2018 to 2019
$145k
NCI NIH HHS P30 CA225520NCI NIH HHS R01 CA154745NCI NIH HHS R03 CA223615NIGMS NIH HHS P20 GM103639
6 · The paper itself

Abstract

ETS variant 1 (ETV1) is an oncogenic transcription factor. However, its role in colorectal cancer has remained understudied. The present study demonstrated that ETV1 downregulation led to reduced HCT116 colorectal cancer cell growth and clonogenic activity. Furthermore, the ETV1 mRNA levels were enhanced in colorectal tumors and were associated with disease severity. In addition, ETV1 directly bound to Jumonji C domain‑containing (JMJD) 1A, a histone demethylase known to promote colon cancer. ETV1 and JMJD1A, but not a catalytically inactive mutant thereof, cooperated in inducing the matrix metalloproteinase (MMP)1 gene promoter that was similar to the cooperation between ETV1 and another histone demethylase, JMJD2A. RNA‑sequencing revealed multiple potential ETV1 target genes in HCT116 cells, including the FOXQ1 and TBX6 transcription factor genes. Moreover, JMJD1A co‑regulated FOXQ1 and other ETV1 target genes, but not TBX6, whereas JMJD2A downregulation had no impact on FOXQ1 as well as TBX6 transcription. Accordingly, the FOXQ1 gene promoter was stimulated by ETV1 and JMJD1A in a cooperative manner, and both ETV1 and JMJD1A bound to the FOXQ1 promoter. Notably, the overexpression of FOXQ1 partially reversed the growth inhibitory effects of ETV1 ablation on HCT116 cells, whereas TBX6 impaired HCT116 cell growth and may thereby dampen the oncogenic activity of ETV1. The latter also revealed for the first time, to the best of our knowledge, a potential tumor suppressive function of TBX6. Taken together, the present study uncovered a ETV1/JMJD1A‑FOXQ1 axis that may drive colorectal tumorigenesis.

Indexed as

Gene Expression Regulation, NeoplasticCarcinogenesisCell ProliferationColorectal NeoplasmsDNA-Binding ProteinsForkhead Transcription FactorsHCT116 CellsHumansJumonji Domain-Containing Histone DemethylasesMatrix Metalloproteinase 1Mutagenesis, Site-DirectedMutationPromoter Regions, GeneticSurvival AnalysisT-Box Domain ProteinsTime FactorsDNA-Binding ProteinsETV1 protein, humanForkhead Transcription FactorsFOXQ1 protein, humanJumonji Domain-Containing Histone DemethylasesKDM3A protein, humanKDM4A protein, humanMatrix Metalloproteinase 1MMP1 protein, humanT-Box Domain ProteinsTBX6 protein, humanTranscription Factorscolorectal cancerETS proteinFOXQ1gene transcriptionJumonji C domain-containing protein

Identifiers

PMID33174020
PMCPMC7646594
OpenAlexW3092953074

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.