Evidence map›Paper›PMID 19946329›Full record

ReviewOncogene2010

The role of COX-2 in intestinal inflammation and colorectal cancer.

D Wang, R N Dubois

Abstract readReview
In one paragraph

Review in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 428 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
428citing papers in PubMed, 4 pooled it
29.2field-weighted citation impact, top 1% 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

428 citing papers in PubMed, 4 syntheses or guidelines pooled it, 859 citations in OpenAlex.

  1. Pooled it
  2. The Anti-Metastatic Role of Aspirin in Cancer: A Systematic Review.International journal of molecular sciences · 2026
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. The Role ofMedicina (Kaunas, Lithuania) · 2020
    Trial
  9. Review
  10. Article
  11. Multitarget Antiproliferative Activity ofMolecules (Basel, Switzerland) · 2026
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Gas entrapping materials for damage control.Advanced drug delivery reviews · 2026
    Review
  18. Review
  19. A comprehensive review ofMedicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Review
  20. Article

368 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

D WangDepartment of Cancer Biology and GI Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030-4009, USA.
R N Dubois
The University of Texas MD Anderson Cancer Center · US

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
THE ROLE OF ENDOCANNABINOIDS AND THEIR RECEPTORS IN COLORECTAL CANCERP01CA077839 · NCI · VANDERBILT UNIVERSITY · PI DUBOIS, RAYMOND N. · 1999 to 2016
$17.8M
Eicosanoids and Intestinal Epithelial Growth RegulationR37DK047297 · NIDDK · VANDERBILT UNIVERSITY · PI DUBOIS, RAYMOND N. · 2003 to 2012
$3.8M
Nuclear Hormone Receptors in Intestinal BiologyR01DK062112 · NIDDK · VANDERBILT UNIVERSITY · PI DUBOIS, RAYMOND N. · 2002 to 2010
$3.0M
NCI NIH HHS P01 CA077839NCI NIH HHS P01-CA-77839NIDDK NIH HHS P30 DK058404NIDDK NIH HHS P30 DK-58404NIDDK NIH HHS R01 DK062112NIDDK NIH HHS R01DK 62112NIDDK NIH HHS R37 DK047297NIDDK NIH HHS R37-DK47297
6 · The paper itself

Abstract

Colorectal cancer (CRC) is a heterogeneous disease, including at least three major forms: hereditary, sporadic and colitis-associated CRC. A large body of evidence indicates that genetic mutations, epigenetic changes, chronic inflammation, diet and lifestyle are the risk factors for CRC. As elevated cyclooxygenase-2 (COX-2) expression was found in most CRC tissue and is associated with worse survival among CRC patients, investigators have sought to evaluate the effects of nonsteroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors (COXIBs) on CRC. The epidemiological studies, clinical trials and animal experiments indicate that NSAIDs are among the most promising chemopreventive agents for this disease. NSAIDs exert their anti-inflammatory and antitumor effects primarily by reducing prostaglandin production by inhibition of COX-2 activity. In this review, we highlight breakthroughs in our understanding of the roles of COX-2 in CRC and inflammatory bowel disease. These recent data provide a rationale for re-evaluating COX-2 as both the prognostic and the predictive marker in a wide variety of malignancies and for renewing the interest in evaluating relative benefits and risk of COXIBs in appropriately selected patients for cancer prevention and treatment.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalColorectal NeoplasmsCyclooxygenase 2DinoprostoneHumansInflammationIntestinal DiseasesAnti-Inflammatory Agents, Non-SteroidalCyclooxygenase 2Dinoprostone

Identifiers

PMID19946329
PMCPMC3181054
OpenAlexW2020430786

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.