Evidence map›Paper›PMID 28104442›Full record

ArticleCancer letters2017

Prostaglandin E2 receptor 4 mediates renal cell carcinoma intravasation and metastasis.

Yushan Zhang, Hamsa Thayele Purayil, Joseph B Black, Francis Fetto, Lauren D Lynch, Jude N Masannat, Yehia Daaka

Abstract read
In one paragraph

Article in Cancer letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Lipids as Targets for Renal Cell Carcinoma Therapy.International journal of molecular sciences · 2023
    Review
  6. Review
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Observational
  12. Eicosanoids in Cancer: Prostaglandin EFrontiers in pharmacology · 2020
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. 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

7 authors at 2 institutions in 1 country.

Yushan ZhangDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Hamsa Thayele PurayilDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Joseph B BlackDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Francis FettoDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Lauren D LynchDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Jude N MasannatDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Yehia DaakaDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA. Electronic address: ydaaka@ufl.edu.
Florida College · USUniversity of Florida · US

Funding

Prostaglandin Receptor Regulation of Kidney CancerR01CA129155 · NCI · UNIVERSITY OF FLORIDA · PI DAAKA, YEHIA · 2008 to 2013
$1.5M
NCI NIH HHS R01 CA129155
6 · The paper itself

Abstract

Treatment options for metastatic renal cell carcinoma (RCC) are limited. In this study, we investigated impact of prostaglandin E2 (PGE2) receptor 4 (EP4) on RCC metastasis. We found that knockdown of EP4 in two RCC cell lines, ACHN and SN12C, does not affect xenograft tumor take or growth rate in mice, but reduces metastasis by decreasing tumor intravasation. Using chick chorioallantoic membrane (CAM) assay, we confirmed that blockade of EP4 signaling inhibits tumor intravasation. In vitro studies associated EP4 expression and activity with RCC cell transendothelial migration (TEM). Gene expression analysis and validation assays showed that EP4 knockdown decreases expression of CD24, a ligand to the adhesion molecule P-selectin. Forced expression of CD24 in EP4 knockdown RCC rescues TEM capacity of the cells. Pharmacologic inhibition or knockdown of endothelial P-selectin blocks EP4-mediated cancer cell TEM, and inhibition of P-selectin prevents RCC tumor intravasation in CAM assay. Our results demonstrate that inhibition of EP4 attenuates the RCC intravasation and metastasis by downregulating CD24 and that P-selectin participates in tumor intravasation, implying a potential for these molecules as therapeutic targets for advanced RCC treatment.

Indexed as

AnimalsCarcinoma, Renal CellCell MovementHumansMaleMiceMice, NudeNeoplasm InvasivenessNeoplasm MetastasisReceptors, Prostaglandin E, EP4 SubtypeSignal TransductionReceptors, Prostaglandin E, EP4 SubtypeCD24EP4IntravasationMetastasisRenal cell carcinoma

Identifiers

PMID28104442
PMCPMC5340307
OpenAlexW2574904092

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.