Evidence map›Paper›PMID 26067154›Full record

ArticleThe American journal of pathology2015

The homeoprotein DLX4 stimulates NF-κB activation and CD44-mediated tumor-mesothelial cell interactions in ovarian cancer.

Dhwani Haria, Bon Quy Trinh, Song Yi Ko, Nicolas Barengo, Jinsong Liu, Honami Naora

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. LncRNAiScience · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Cancers · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. MutatedCancers · 2019
    Article
  15. Article
  16. Article
  17. CTD-2020K17.1, a Novel Long Non-Coding RNA, Promotes Migration, Invasion, and Proliferation of Serous Ovarian Cancer Cells In Vitro.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  18. Article
  19. Article
  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

6 authors at 1 institution in 1 country.

Dhwani HariaDepartment of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Bon Quy TrinhDepartment of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Song Yi KoDepartment of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Nicolas BarengoDepartment of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Jinsong LiuDepartment of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Honami NaoraDepartment of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas. Electronic address: hnaora@mdanderson.org.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Multifunctional roles of homeobox gene DLX4 in ovarian cancerR01CA141078 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI NAORA, HONAMI · 2010 to 2014
$1.6M
NCI NIH HHS CA141078NCI NIH HHS R01 CA141078
6 · The paper itself

Abstract

Ovarian cancers often highly express inflammatory cytokines and form implants throughout the peritoneal cavity. However, the mechanisms that drive inflammatory signaling and peritoneal metastasis of ovarian cancer are poorly understood. We previously identified that high expression of DLX4, a transcription factor encoded by a homeobox gene, is associated with reduced survival of ovarian cancer patients. In this study, we identified that DLX4 stimulates attachment of ovarian tumor cells to peritoneal mesothelial cells in vitro and increases the numbers of peritoneal implants in xenograft models. DLX4 induced expression of the cell surface molecule CD44 in ovarian tumor cells, and inhibition of CD44 abrogated the ability of DLX4 to stimulate tumor-mesothelial cell interactions. The induction of CD44 by DLX4 was attributed to increased activity of NF-κB that was stimulated by the inflammatory cytokine IL-1β, a transcriptional target of DLX4. The stimulatory effects of DLX4 on CD44 levels and tumor-mesothelial cell interactions were abrogated when IL-1β or NF-κB was inhibited in tumor cells. Furthermore, DLX4 expression levels strongly correlated with NF-κB activation and disease stage in clinical specimens of ovarian cancer. Collectively, these findings indicate that DLX4 induces CD44 by stimulating IL-1β-mediated NF-κB activity, thereby promoting peritoneal metastasis of ovarian cancer.

Indexed as

AnimalsCell AdhesionCell Line, TumorEpithelial CellsFemaleHomeodomain ProteinsHumansHyaluronan ReceptorsInterleukin-1betaMiceMice, NudeNeoplasm MetastasisNF-kappa BOvarian NeoplasmsPeritoneumPhosphorylationDLX4 protein, humanHomeodomain ProteinsHyaluronan ReceptorsInterleukin-1betaNF-kappa BTranscription Factors

Identifiers

PMID26067154
PMCPMC4530135
OpenAlexW2104152276

What OpenQuestion holds

Textmetadata
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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.