Evidence map›Paper›PMID 20858737›Full record

ArticleMolecular cancer research : MCR2010

Prostaglandin E receptor EP1 suppresses breast cancer metastasis and is linked to survival differences and cancer disparities.

Xinrong Ma, Namita Kundu, Olga B Ioffe, Olga Goloubeva, Raymond Konger, Claudia Baquet, Phyllis Gimotty, Jocelyn Reader, Amy M Fulton

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Molecular cancer research : MCR, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  16. Microenvironmental Influences on Metastasis Suppressor Expression and Function during a Metastatic Cell's Journey.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2014
    Article
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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

9 authors at 4 institutions in 1 country.

Xinrong MaUniversity of Maryland, Greenebaum Cancer Center, Baltimore, MD 21201, USA.
Namita Kundu
Olga B Ioffe
Olga Goloubeva
Raymond Konger
Claudia Baquet
Phyllis Gimotty
Jocelyn Reader
Amy M Fulton
University of Maryland, Baltimore · USIndiana University – Purdue University Indianapolis · USUniversity of Pennsylvania · USIndiana University School of Medicine

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

Cyclooxygenase-2 is frequently overexpressed and associated with poor prognosis in breast cancer. The cyclooxygenase-2 product prostaglandin E(2) elicits cellular responses through four G-protein-coupled receptors, designated EP1 to EP4, coupled to distinct intracellular signaling pathways. EP4, expressed on malignant breast cells, promotes metastasis; however, a role for EP1 in metastasis has not been investigated. Using a murine model of metastatic breast cancer, we now show that pharmacologic antagonism of EP1 with SC19220 or AH6809 promoted lung colonization of mammary tumor cells by 3.7- to 5.4-fold. Likewise, reducing EP1 gene expression by shRNA also increased metastatic capacity relative to cells transfected with nonsilencing vector but did not affect the size of transplanted tumors. Examination of invasive ductal carcinomas by immunohistochemistry shows that EP1 was detected in both the cytoplasm and nucleus of benign ducts as well as malignant cells in some samples, but was absent or limited to either the nucleus or cytoplasm in other malignant samples. Overall survival for women with tumors that were negative for nuclear EP1 was significantly worse than for women with EP1 expression (P = 0.008). There was no difference in survival for women with differences in cytoplasmic EP1 expression (P = 0.46). Comparing EP1 mRNA in breast tumors from African American and European American women revealed that many more African American breast tumors lacked detectable EP1 mRNA (P = 0.04). These studies support the hypothesis that EP1 functions as a metastasis suppressor and that loss of nuclear EP1 is associated with poorer overall survival and may contribute to disparities in outcome in different populations.

Indexed as

AnimalsBiomarkers, TumorBreast NeoplasmsCell Line, TumorDisease Models, AnimalFemaleHumansLung NeoplasmsMiceMice, Inbred BALB CNuclear ProteinsPrognosisReceptors, Prostaglandin E, EP1 SubtypeSurvival RateTumor Suppressor ProteinsBiomarkers, TumorNuclear ProteinsReceptors, Prostaglandin E, EP1 SubtypeTumor Suppressor Proteins

Identifiers

PMID20858737
PMCPMC2974016
OpenAlexW2170955100

What OpenQuestion holds

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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.