Evidence map›Paper›PMID 23029040›Full record

ArticlePloS one2012

15-lipoxygenase metabolites of docosahexaenoic acid inhibit prostate cancer cell proliferation and survival.

Joseph T O'Flaherty, Yungping Hu, Rhonda E Wooten, David A Horita, Michael P Samuel, Michael J Thomas, Haiguo Sun, Iris J Edwards

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.9field-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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. The role of 5-lipoxygenase in the pathophysiology of COVID-19 and its therapeutic implications.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Review
  9. Assessing the safety of transarterial locoregional delivery of low-density lipoprotein docosahexaenoic acid nanoparticles to the rat liver.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2021
    Article
  10. Review
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  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Mammalian lipoxygenases and their biological relevance.Biochimica et biophysica acta · 2015
    Review
  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

8 authors at 1 institution in 1 country.

Joseph T O'FlahertyDepartment of Internal Medicine Wake Forest School of Medicine, Winston-Salem, NC, USA.
Yungping Hu
Rhonda E Wooten
David A Horita
Michael P Samuel
Michael J Thomas
Haiguo Sun
Iris J Edwards
Wake Forest University · US

Funding

Phospholipid Signaling in Fish oil-induced Growth Inhibition of Prostate CancerP01CA106742 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CHEN, YONG Q · 2006 to 2010
$5.0M
Structural Basis of Membrane Targeting by NADPH OxidaseR01AI064609 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HORITA, DAVID A · 2005 to 2010
$1.8M
Regulation of syndecan 1 in by n-3 PUFAR01CA115958 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI EDWARDS, IRIS J · 2005 to 2009
$1.0M
NCI NIH HHS CA1207NCI NIH HHS P01 CA106742NCI NIH HHS P01CA106742NCI NIH HHS R01 CA115958NCI NIH HHS R01CA115958NIAID NIH HHS R01 AI064609NIAID NIH HHS R01AI064609
6 · The paper itself

Abstract

A 15-LOX, it is proposed, suppresses the growth of prostate cancer in part by converting arachidonic, eicosatrienoic, and/or eicosapentaenoic acids to n-6 hydroxy metabolites. These metabolites inhibit the proliferation of PC3, LNCaP, and DU145 prostate cancer cells but only at ≥1-10 µM. We show here that the 15-LOX metabolites of docosahexaenoic acid (DHA), 17-hydroperoxy-, 17-hydroxy-, 10,17-dihydroxy-, and 7,17-dihydroxy-DHA inhibit the proliferation of these cells at ≥0.001, 0.01, 1, and 1 µM, respectively. By comparison, the corresponding 15-hydroperoxy, 15-hydroxy, 8,15-dihydroxy, and 5,15-dihydroxy metabolites of arachidonic acid as well as DHA itself require ≥10-100 µM to do this. Like DHA, the DHA metabolites a) induce PC3 cells to activate a peroxisome proliferator-activated receptor-γ (PPARγ) reporter, express syndecan-1, and become apoptotic and b) are blocked from slowing cell proliferation by pharmacological inhibition or knockdown of PPARγ or syndecan-1. The DHA metabolites thus slow prostate cancer cell proliferation by engaging the PPARγ/syndecan-1 pathway of apoptosis and thereby may contribute to the prostate cancer-suppressing effects of not only 15-LOX but also dietary DHA.

Indexed as

ApoptosisArachidonate 15-LipoxygenaseCaspasesCell Line, TumorCell ProliferationCell SurvivalDocosahexaenoic AcidsHumansMalePPAR gammaProstatic NeoplasmsSignal TransductionSyndecan-1Arachidonate 15-LipoxygenaseCaspasesDocosahexaenoic AcidsPPAR gammaSyndecan-1

Identifiers

PMID23029040
PMCPMC3447860
OpenAlexW1997282786

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.