Evidence map›Paper›PMID 17640394›Full record

ReviewBreast cancer research : BCR2007

Inflammation and breast cancer. Cyclooxygenase/prostaglandin signaling and breast cancer.

Louise R Howe

Open access · goldAbstract readReview
In one paragraph

Review in Breast cancer research : BCR, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 150 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
150citing papers in PubMed, 3 pooled it
12.0field-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

150 citing papers in PubMed, 3 syntheses or guidelines pooled it, 294 citations in OpenAlex.

  1. Pooled it
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  4. Trial
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  6. Review
  7. Article
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  12. Prostaglandin E2 receptor EP1 expression in vulvar cancer.Journal of cancer research and clinical oncology · 2023
    Article
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90 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

1 author at 1 institution in 1 country.

Louise R HoweDepartment of Cell & Developmental Biology, Weill Medical College of Cornell University, York Avenue, New York, New York 10021, USA. lrhowe@med.cornell.edu
Cornell University · US

Funding

PREVENTION OF BREAST CANCER USING SELECTIVE RETINOIDSR01CA078480 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BROWN, POWEL H · 1999 to 2008
$3.1M
NEW THARAPY FOR HER 2/NEU POSITIVE BREAST CANCERR01CA089578 · NCI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI DANNENBERG, ANDREW JESS · 2001 to 2004
$1.1M
Aspirin for Breast Cancer PreventionR03CA119273 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI HOWE, LOUISE R · 2005 to 2006
$166k
NCI NIH HHS R01 CA078480NCI NIH HHS R01 CA089578NCI NIH HHS R03 CA119273
6 · The paper itself

Abstract

Many human cancers exhibit elevated prostaglandin (PG) levels due to upregulation of cyclooxygenase-2 (COX-2), a key enzyme in eicosanoid biosynthesis. COX-2 over-expression has been observed in about 40% of cases of invasive breast carcinoma and at a higher frequency in preinvasive ductal carcinoma in situ tumors, Extensive pharmacologic and genetic evidence implicates COX enzymes in neoplasia. Epidemiologic analyses demonstrate a protective effect of COX-inhibiting nonsteroidal anti-inflammatory drugs with respect to human cancer. Complementary experimental studies have established that both conventional nonsteroidal anti-inflammatory drugs and selective COX-2 inhibitors suppress mammary tumor formation in rodent breast cancer models. Furthermore, knocking out Cox-2 reduces mammary tumorigenesis and angiogenesis, and, conversely, transgenic COX-2 over-expression induces tumor formation. The utility of COX/PG signaling as a target for chemoprevention has been established by randomized controlled clinical trials. However, these studies also identified increased cardiovascular risk associated with use of selective COX-2 inhibitors. Thus, current efforts are directed toward identifying safer approaches to antagonizing COX/PG signaling for cancer prevention and treatment, with a particular focus on PGE2 regulation and signaling, because PGE2 is a key pro-tumorigenic prostanoid.

Indexed as

Breast NeoplasmsCyclooxygenase 2Cyclooxygenase 2 InhibitorsHumansInflammationProstaglandinsSignal TransductionCyclooxygenase 2Cyclooxygenase 2 InhibitorsProstaglandins

Identifiers

PMID17640394
PMCPMC2206709
OpenAlexW2070732038

What OpenQuestion holds

Textmetadata
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.