Evidence map›Paper›PMID 20159031›Full record

ReviewBiochimie2010

mPGES-1 as a target for cancer suppression: A comprehensive invited review "Phospholipase A2 and lipid mediators".

Masako Nakanishi, Vijay Gokhale, Emmanuelle J Meuillet, Daniel W Rosenberg

Open access · greenAbstract readReview
In one paragraph

Review in Biochimie, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. COX-2-PGEArchives of gynecology and obstetrics · 2020
    Review
  11. Article
  12. Selenium and selenoproteins in prostanoid metabolism and immunity.Critical reviews in biochemistry and molecular biology · 2019
    Review
  13. Article
  14. Preventive effect ofJournal of clinical biochemistry and nutrition · 2018
    Article
  15. Article
  16. Expression of prostaglandin E2 and EP receptors in human papillary thyroid carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  17. Review
  18. BioMed research international · 2016
    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

4 authors at 2 institutions in 1 country.

Masako NakanishiCenter for Molecular Medicine, University of Connecticut Health Center, 263 Farmington Ave., Farmington, CT 06030-3101, USA.
Vijay Gokhale
Emmanuelle J Meuillet
Daniel W Rosenberg
UConn Health · USUniversity of Arizona · US

Funding

Are ACF Surrogate Markers for Chemoprevention?R01CA159976 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ROSENBERG, DANIEL WILLIAM · 2012 to 2016
$1.9M
Using Mouse Endoscopy for Evaluating Colon CancerR01CA125691 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ROSENBERG, DANIEL WILLIAM · 2008 to 2012
$1.8M
Inhibition of novel molecular targets of prostaglandin formation for antitumor acR01CA138702 · NCI · UNIVERSITY OF ARIZONA · PI MEUILLET, EMMANUELLE JOELLE · 2010 to 2014
$1.6M
Altered Arachidonic Acid Balance and Colon CancerR01CA114635 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ROSENBERG, DANIEL WILLIAM · 2006 to 2010
$1.6M
NCI NIH HHS 5R01CA114635NCI NIH HHS R01 CA114635NCI NIH HHS R01 CA125691NCI NIH HHS R01 CA138702NCI NIH HHS R01 CA159976
6 · The paper itself

Abstract

Prostaglandin E(2) (PGE(2)) is a bioactive lipid that can elicit a wide range of biological effects associated with inflammation and cancer. The physiological roles of PGE(2) are diverse, mediated in part through activation of key downstream signaling cascades via transmembrane EP receptors located on the cell surface. Elevated levels of COX-2 and concomitant overproduction of PGE(2) are often found in human cancers. These observations have led to the use of non-steroidal anti-inflammatory drugs (NSAIDs) as chemopreventive agents, particularly for colorectal cancer (CRC). Their long-term use, however, may be associated with gastrointestinal toxicity and increased risk of adverse cardiovascular events, prompting the development of other enzymatic targets in this pathway. This review will focus on recent efforts to target the terminal synthase, mPGES-1, for cancer chemoprevention. The role of mPGES-1 in the pathogenesis of various cancers is discussed. In addition, an overview of recent efforts to develop small molecule inhibitors that target the protein with high selectivity is also be reviewed.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalHumansIntramolecular OxidoreductasesNeoplasmsPhospholipase A2 InhibitorsPhospholipases A2Prostaglandin-E SynthasesAnti-Inflammatory Agents, Non-SteroidalIntramolecular OxidoreductasesPhospholipase A2 InhibitorsPhospholipases A2Prostaglandin-E SynthasesPTGES protein, human

Identifiers

PMID20159031
PMCPMC2898715
OpenAlexW1552554367

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.