Evidence map›Paper›PMID 25433169›Full record

ReviewProstaglandins & other lipid mediators

Multiple drug resistance-associated protein 4 (MRP4), prostaglandin transporter (PGT), and 15-hydroxyprostaglandin dehydrogenase (15-PGDH) as determinants of PGE2 levels in cancer.

Tyler J Kochel, Amy M Fulton

Abstract readReview
In one paragraph

Review in Prostaglandins & other lipid mediators. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. [Metabolism and transport pathway of prostaglandin E2 and its role in liver regeneration].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2021
    Review
  9. Article
  10. Prostaglandin EGenes to cells : devoted to molecular & cellular mechanisms · 2020
    Article
  11. Review
  12. Article
  13. Article
  14. Eicosanoids and cancer.Clinics (Sao Paulo, Brazil) · 2018
    Article
  15. Article
  16. Munc13 proteins control regulated exocytosis in mast cells.The Journal of biological chemistry · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 2 institutions in 1 country.

Tyler J KochelUniversity of Maryland, Baltimore, Baltimore, MD, USA. Electronic address: tkoch001@umaryland.edu.
Amy M FultonDepartment of Pathology, University of Maryland, Baltimore, Baltimore, MD, USA; Baltimore Veterans Affairs Medical Center, Baltimore, MD, USA. Electronic address: afulton@umaryland.edu.
University of Baltimore · USVeterans Health Administration · US

Funding

UNIVERSITY OF MARYLAND GREENEBAUM CANCER CENTERSUPPORT GRANTP30CA134274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI FEYRUZ VIRGILIA RASSOOL · 2008 to 2026
$51.0M
Cyclooxygenase Modulators of Immune Function in Breast CancerR01CA120278 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI FULTON, AMY M. · 2007 to 2011
$1.5M
Targeting the COX-2 Pathway to Reduce Breast Cancer MortalityI01BX000169 · VA · BALTIMORE VA MEDICAL CENTER · PI FULTON, AMY M. · 2009 to 2020
–
BLRD VA I01 BX000169NCI NIH HHS P30 CA134274NCI NIH HHS R01 CA120278
6 · The paper itself

Abstract

The cyclooxygenase-2 (COX-2) enzyme and major lipid product, prostaglandin E2 (PGE2) are elevated in many solid tumors including those of the breast and are associated with a poor prognosis. Targeting this enzyme is somewhat effective in preventing tumor progression, but is associated with cardiotoxic secondary effects when used chronically. PGE2 functions by signaling through four EP receptors (EP1-4), resulting in several different cellular responses, many of which are pro-tumorigenic, and there is growing interest in the therapeutic potential of targeting EP4 and EP2. Other members in this signaling pathway are gaining more attention. PGE2 is transported out of and into cells by two unique transport proteins. Multiple Drug Resistance-Associated Protein 4 (MRP4) and Prostaglandin Transporter (PGT) modulate PGE2 signaling by increasing or decreasing the levels of PGE2 available to cells. 15-hydroxyprostaglandin dehydrogenase (15-PGDH) metabolizes PGE2 and silences the pathway in this manner. The purpose of this review is to summarize the extensive data supporting the importance of the COX-2 pathway in tumor biology with a focus on more recently described pathway members and their role in modulating PGE2 signaling. This review describes evidence supporting roles for MRP4, PGT and 15-PGDH in several tumor types with an emphasis on the roles of these proteins in breast cancer. Defining the importance of these latter pathway members will be key to developing new therapeutic approaches that exploit the tumor-promoting COX-2 pathway.

Indexed as

AnimalsATP-Binding Cassette, Sub-Family C ProteinsDinoprostoneHumansHydroxyprostaglandin DehydrogenasesNeoplasm ProteinsNeoplasmsOrganic Anion Transporters15-hydroxyprostaglandin dehydrogenaseABCC4 protein, humanATP-Binding Cassette, Sub-Family C ProteinsDinoprostoneHydroxyprostaglandin DehydrogenasesNeoplasm ProteinsOrganic Anion TransportersSLCO2A1 protein, human15-Hydroxyprostaglandin dehydrogenaseCyclooxygenase 2Multidrug resistance-associated protein 4Prostaglandin E2Prostaglandin transporter

Identifiers

PMID25433169
PMCPMC4385402
OpenAlexW2064131567

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.