Evidence map›Paper›PMID 25972361›Full record

ArticleOncotarget2015

Aberrant over-expression of COX-1 intersects multiple pro-tumorigenic pathways in high-grade serous ovarian cancer.

Andrew J Wilson, Oluwole Fadare, Alicia Beeghly-Fadiel, Deok-Soo Son, Qi Liu, Shilin Zhao, Jeanette Saskowski, Md Jashim Uddin, Cristina Daniel, Brenda Crews and 5 more

Abstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. RepurposingJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Article
  10. Article
  11. Targeted Detection of Cyclooxygenase-1 in Ovarian Cancer.ACS medicinal chemistry letters · 2020
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

15 authors.

Andrew J WilsonDepartment of Obstetrics & Gynecology, Vanderbilt University Medical Center, Nashville, TN, USA.
Oluwole FadareDepartment of Pathology, University of California San Diego School of Medicine, La Jolla, CA, USA.
Alicia Beeghly-FadielDepartment of Medicine, Division of Epidemiology, Vanderbilt University Medical Center, Nashville, TN, USA.
Deok-Soo SonDepartment of Biochemistry & Cancer Biology, Meharry Medical College, Nashville, TN, USA.
Qi LiuDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
Shilin ZhaoVanderbilt Center for Quantitative Sciences, Vanderbilt University School of Medicine, Nashville, TN, USA.
Jeanette SaskowskiDepartment of Obstetrics & Gynecology, Vanderbilt University Medical Center, Nashville, TN, USA.
Md Jashim UddinDepartment of Biochemistry, Vanderbilt University Medical Center, Nashville, TN, USA.
Cristina DanielDepartment of Biochemistry, Vanderbilt University Medical Center, Nashville, TN, USA.
Brenda CrewsDepartment of Biochemistry, Vanderbilt University Medical Center, Nashville, TN, USA.
Brian D LehmannVanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN, USA.
Jennifer A PietenpolVanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN, USA.
Marta A CrispensDepartment of Obstetrics & Gynecology, Vanderbilt University Medical Center, Nashville, TN, USA.
Lawrence J MarnettVanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN, USA.
Dineo KhabeleDepartment of Obstetrics & Gynecology, Vanderbilt University Medical Center, Nashville, TN, USA.

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
VITAMIN D DEFICIENCY AND INCREASED RISK OF UTERINE FIBROIDS IN AFRICAN AMERICANSG12RR003032 · NCRR · MEHARRY MEDICAL COLLEGE · PI RAO, UMA · 1985 to 2011
$27.4M
ROLES OF STATS AND SRC KINASES IN GROWTH CONTROL BY IL17U54CA091408 · NCI · MEHARRY MEDICAL COLLEGE · PI ADUNYAH, SAMUEL EVANS · 2001 to 2010
$20.2M
VANTAGE:Consolidation to create the Vanderbilt Technologies for Advanced GenomicsG20RR030956 · NCRR · VANDERBILT UNIVERSITY · PI PIETENPOL, JENNIFER A · 2010 to 2010
$8.7M
Roles of inflammation-driven chemokines in the pathogenesis of ovarian cancerSC1AI089073 · NIAID · MEHARRY MEDICAL COLLEGE · PI SON, DEOK-SOO · 2009 to 2013
$1.8M
Targeting Histone Deacetylases with Small Moleule Inhibitors in Ovarian CancerK08CA148887 · NCI · VANDERBILT UNIVERSITY · PI KHABELE, DINEO · 2010 to 2014
$795k
NCATS NIH HHS UL1 TR000445NCATS NIH HHS UL1TR000445NCI NIH HHS 5P30 CA068485NCI NIH HHS CA091408 5 U54NCI NIH HHS K08 CA148887NCI NIH HHS K08CA148887-05NCI NIH HHS P30 CA068485NCI NIH HHS U54 CA091408NCRR NIH HHS 1UL1 RR024975NCRR NIH HHS G12 RR003032NCRR NIH HHS G20 RR030956NCRR NIH HHS UL1 RR024975NIAID NIH HHS SC1 AI089073NIAID NIH HHS SC1AI089073
6 · The paper itself

Abstract

Cyclooxygenase-1 (COX-1) is implicated in ovarian cancer. However, patterns of COX expression and function have been unclear and controversial. In this report, patterns of COX-1 and COX-2 gene expression were obtained from RNA-seq data through The Cancer Genome Atlas. Our analysis revealed markedly higher COX-1 mRNA expression than COX-2 in high-grade serous ovarian cancers (HGSOC) and higher COX-1 expression in HGSOC tumors than 10 other tumor types. High expression of COX-1 in HGSOC tumors was confirmed in an independent tissue microarray. In contrast, lower or similar expression of COX-1 compared to COX-2 was observed in endometrioid, mucinous and clear cell tumors. Stable COX-1 knockdown in HGSOC-representative OVCAR-3 ovarian cancer cells reduced gene expression in multiple pro-tumorigenic pathways. Functional cell viability, clonogenicity, and migration/invasion assays were consistent with transcriptomic changes. These effects were reversed by stable over-expression of COX-1 in SKOV-3 cells. Our results demonstrate a distinct pattern of COX-1 over-expression in HGSOC tumors and strong association of COX-1 with multiple pro-tumorigenic pathways in ovarian cancer cells. These findings provide additional insight into the role of COX-1 in human ovarian cancer and support further development of methods to selectively target COX-1 in the management of HGSOC tumors.

Indexed as

Gene Expression ProfilingGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticCarcinoma, Ovarian EpithelialCell Line, TumorCell MovementCell ProliferationComputational BiologyCyclooxygenase 1FemaleGenome, HumanHumansImmunohistochemistryNeoplasm InvasivenessNeoplasms, Glandular and EpithelialNeovascularization, PathologicCyclooxygenase 1PTGS1 protein, humancell migration/invasioncyclooxygenase-1high-grade serous ovarian cancerpro-tumorigenic pathways

Identifiers

PMID25972361
PMCPMC4673270

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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.