Evidence map›Paper›PMID 20178979›Full record

ArticleThe Journal of biological chemistry2010

The anti-tumorigenic properties of peroxisomal proliferator-activated receptor alpha are arachidonic acid epoxygenase-mediated.

Ambra Pozzi, Vlad Popescu, Shilin Yang, Shaojun Mei, Mingjian Shi, Satu M Puolitaival, Richard M Caprioli, Jorge H Capdevila

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

55 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
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  9. Repurposing antifungal drugs for cancer therapy.Journal of advanced research · 2023
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  14. Article
  15. Assessing cytochrome P450 function using genetically engineered mouse models.Advances in pharmacology (San Diego, Calif.) · 2022
    Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review
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

8 authors at 1 institution in 1 country.

Ambra PozziDepartment of Medicine, Vanderbilt University Medical School, Nashville, Tennessee 37232, USA.
Vlad Popescu
Shilin Yang
Shaojun Mei
Mingjian Shi
Satu M Puolitaival
Richard M Caprioli
Jorge H Capdevila
Vanderbilt University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
TRANSPORT EFFECTS OF ARACHIDONATE METABOLITES IN PERFUSED TUBULEP01DK038226 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BROWN, NANCY J. · 1986 to 2015
$22.1M
TYPE IV COLLAGEN, LAMININS, AND INTEGRINS IN NORMAL AND DISEASED GLOMERULIP01DK065123 · NIDDK · VANDERBILT UNIVERSITY · PI HUDSON, BILLY GERALD · 2003 to 2012
$12.9M
Spatial Analysis of Molecules in Tissue using MALDI-MSR01GM058008 · NIGMS · VANDERBILT UNIVERSITY · PI CAPRIOLI, RICHARD M · 1998 to 2015
$5.8M
NADPH-DEPENDENT METABOLISM OF ARACHIDONIC ACIDR01GM037922 · NIGMS · VANDERBILT UNIVERSITY · PI CAPDEVILA, JORGE · 1986 to 2008
$2.6M
NCI NIH HHS CA-68485NCI NIH HHS P30 CA068485NIDDK NIH HHS DK 5P01-038226NIDDK NIH HHS DK R01-065123NIDDK NIH HHS P01 DK038226NIGMS NIH HHS GM 5R01-037922NIGMS NIH HHS GM5R01-58008
6 · The paper itself

Abstract

Prevalence and mortality make cancer a health challenge in need of effective and better tolerated therapeutic approaches, with tumor angiogenesis identified as a promising target for drug development. The epoxygenase products, the epoxyeicosatrienoic acids, are pro-angiogenic, and down-regulation of their biosynthesis by peroxisomal proliferator-activated receptor alpha (PPARalpha) ligands reduces tumor angiogenesis and growth. Endothelial cells lacking a Cyp2c44 epoxygenase, a PPARalpha target, show reduced proliferative and tubulogenic activities that are reversed by the enzyme's metabolites. In a mouse xenograft model of tumorigenesis, disruption of the host Cyp2c44 gene causes marked reductions in tumor volume, mass, and vascularization. The relevance of these studies to human cancer is indicated by the demonstration that: (a) activation of human PPARalpha down-regulates endothelial cell CYP2C9 epoxygenase expression and blunts proliferation and tubulogenesis, (b) in a PPARalpha-humanized mouse model, activation of the receptor inhibits tumor angiogenesis and growth, and (c) the CYP2C9 epoxygenase is expressed in the vasculature of human tumors. The identification of anti-angiogenic/anti-tumorigenic properties of PPARalpha points to a role for the receptor and its epoxygenase regulatory target in the pathophysiology of cancer, and for its ligands as candidates for the development of a new generation of safer and better tolerated anti-cancer drugs.

Indexed as

Gene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticAnimalsCell ProliferationCytochrome P-450 Enzyme SystemCytochrome P450 Family 2Drug Screening Assays, AntitumorEndothelium, VascularHumansMiceMice, KnockoutNeoplasm ProteinsNeoplasms, ExperimentalNeoplasm TransplantationNeovascularization, PathologicPPAR alphaCyp2c23 protein, mouseCytochrome P-450 Enzyme SystemCytochrome P450 Family 2Neoplasm ProteinsPPAR alpha

Identifiers

PMID20178979
PMCPMC2857132
OpenAlexW2029715362

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.