Evidence map›Paper›PMID 18767115›Full record

ArticleJournal of cellular biochemistry2008

Migratory activity of human breast cancer cells is modulated by differential expression of xanthine oxidoreductase.

Mehdi A Fini, David Orchard-Webb, Beata Kosmider, Jeremy D Amon, Robert Kelland, Gayle Shibao, Richard M Wright

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Scientific reports · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Establishing pteridine metabolism in a progressive isogenic breast cancer cell model - part II.Metabolomics : Official journal of the Metabolomic Society · 2022
    Article
  10. Article
  11. Establishing pteridine metabolism in a progressive isogenic breast cancer cell model.Metabolomics : Official journal of the Metabolomic Society · 2021
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Predicting ovarian cancer recurrence by plasma metabolic profiles before and after surgery.Metabolomics : Official journal of the Metabolomic Society · 2018
    Article
  18. Alcohol abuse is associated with enhanced pulmonary and systemic xanthine oxidoreductase activity.American journal of physiology. Lung cellular and molecular physiology · 2017
    Article
  19. Article
  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

7 authors at 4 institutions in 2 countries.

Mehdi A FiniWebb-Waring Institute for Cancer, Aging and Antioxidant Research, 4200 East 9th Ave, Denver, Colorado 80262, USA.
David Orchard-Webb
Beata Kosmider
Jeremy D Amon
Robert Kelland
Gayle Shibao
Richard M Wright
University of Bath · GBUniversity of Colorado Denver · USNational Jewish Health · USPrinceton University · US

Funding

Respiratory Endothelial Injury by Xanthine OxideR01HL045582 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI REPINE, JOHN E · 1992 to 2010
$3.4M
Colorado Summer Research Training for Undergraduate DiversityR25HL108823 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI JOHN E REPINE · 2011 to 2026
$864k
NHLBI NIH HHS R01 HL045582NHLBI NIH HHS R01-HL045582NHLBI NIH HHS R25 HL108823
6 · The paper itself

Abstract

Xanthine oxidoreductase (XOR) may exert an important, but poorly defined, role in the pathogenesis of breast cancer (BC). Loss of XOR expression was linked to aggressive BC, and recent clinical observations have suggested that decreasing XOR may be functionally linked to BC aggressiveness. The goal of the present investigation was to determine whether the decreased XOR observed in clinically aggressive BC was an intrinsic property of highly invasive mammary epithelial cells (MEC). Expression of XOR was investigated using HC11 mouse MEC, HB4a and MCF-10A normal human MEC, and several human mammary tumor cells including MCF-7 and MDA-MB-231. Consistent with clinical observations, data shown here revealed high levels of XOR in normal HC11 and MCF-10A cells that was markedly reduced in highly invasive mammary tumor cells. The contribution of XOR to tumor cell migration in vitro was investigated using MDA-MB-231 and MCF-7 cells and clonally selected derivatives of HC11 that exhibit either weak or strong migration in vitro. We observed that over-expression of an XOR cDNA in MDA-MB-231 and in HC11-C24, both possessing weak XOR expression and high migratory capacity, inhibited their migration in vitro. Conversely, pharmacological inhibition of XOR in MCF-7 and HC11-C4, both possessing high XOR expression and weak migratory capacity, stimulated their migration in vitro. Further experiments suggested that XOR derived ROS mediated this effect and also modulated COX-2 and MMP levels and function. These data demonstrate a functional link between XOR expression and MEC migration and suggest a potential role for XOR in suppressing BC pathogenesis.

Indexed as

Cell MovementGene Expression Regulation, NeoplasticAnimalsBreast NeoplasmsCell Line, TumorDNA, ComplementaryHumansMammary Glands, AnimalMammary Glands, HumanMiceTransfectionXanthine DehydrogenaseDNA, ComplementaryXanthine Dehydrogenase

Identifiers

PMID18767115
PMCPMC2587521
OpenAlexW2138702740

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.