Evidence map›Paper›PMID 29482584›Full record

ArticleJournal of ovarian research2018

Differential cyclooxygenase expression levels and survival associations in type I and type II ovarian tumors.

Alicia Beeghly-Fadiel, Andrew J Wilson, Spencer Keene, Meral El Ramahi, Shu Xu, Lawrence J Marnett, Oluwole Fadare, Marta A Crispens, Dineo Khabele

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.7field-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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. RepurposingJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Urinary PGE-M Levels and Risk of Ovarian Cancer.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2019
    Article
  15. 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

9 authors at 3 institutions in 1 country.

Alicia Beeghly-FadielDepartment of Medicine, Division of Epidemiology, Vanderbilt Epidemiology Center, Institute for Medicine and Public Health, Vanderbilt University Medical Center, Nashville, TN, USA.
Andrew J WilsonDepartment of Obstetrics & Gynecology, Division of Gynecologic Oncology, Vanderbilt University Medical Center, Nashville, TN, USA.
Spencer KeeneDepartment of Medicine, Division of Epidemiology, Vanderbilt Epidemiology Center, Institute for Medicine and Public Health, Vanderbilt University Medical Center, Nashville, TN, USA.
Meral El RamahiDepartment of Obstetrics & Gynecology, Division of Gynecologic Oncology, Vanderbilt University Medical Center, Nashville, TN, USA.
Shu XuDepartment of Biochemistry, Vanderbilt University Medical Center, Nashville, TN, USA.
Lawrence J MarnettDepartment of Biochemistry, Vanderbilt University Medical Center, Nashville, TN, USA.
Oluwole FadareDepartment of Pathology, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Marta A CrispensVanderbilt-Ingram Cancer Center, Nashville, TN, USA.
Dineo KhabeleDepartment of Obstetrics and Gynecology, Division of Gynecologic Oncology, The University of Kansas Medical Center, MS 2028, 3901 Rainbow Boulevard, Kansas City, KS, 66160, USA. dkhabele@kumc.edu.
Vanderbilt University Medical Center · USUniversity of California, San Diego · USUniversity of Kansas Medical Center · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
ROLES OF STATS AND SRC KINASES IN GROWTH CONTROL BY IL17U54CA091408 · NCI · MEHARRY MEDICAL COLLEGE · PI ADUNYAH, SAMUEL EVANS · 2001 to 2010
$20.2M
FUNCTIONAL ANALYSIS OF CYCLOOXYGENASE 2R01CA089450 · NCI · VANDERBILT UNIVERSITY · PI MARNETT, LAWRENCE J. · 2001 to 2016
$6.3M
Targeting Histone Deacetylases with Small Moleule Inhibitors in Ovarian CancerK08CA148887 · NCI · VANDERBILT UNIVERSITY · PI KHABELE, DINEO · 2010 to 2014
$795k
Leica Bond RXS10OD023475 · OD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BOYD, KELLI L. · 2018 to 2018
$213k
NCI NIH HHS 2P30 CA06848NCI NIH HHS K08 CA148887NCI NIH HHS P30 CA068485NCI NIH HHS R01 CA089450NCI NIH HHS U54 CA091408NCRR NIH HHS UL1 RR024975NIH HHS 2R01 CA089450NIH HHS 5P30 CA068485NIH HHS CA091408 5 U54NIH HHS K08CA148887NIH HHS S10 OD023475NIMH NIH HHS 1UL1 RR024975
6 · The paper itself

Abstract

backgroundHigh cyclooxygenase (COX)-2 expression in ovarian tumors has been associated with poor prognosis, but the role of COX-1 expression and its relation to survival is less clear. Here, we evaluated COX expression and associations with survival outcomes between type I (clear cell, mucinous, low grade endometrioid and low grade serous) and type II (high grade serous and high grade endometrioid) ovarian tumors.

methodsWe developed and validated a new COX-1 antibody, and conducted immunohistochemical (IHC) staining for COX-1 and COX-2 on a tissue microarray (TMA) of 190 primary ovarian tumors. In addition to standard IHC scoring and H-scores to combine the percentage of positive cells and staining intensity, we also measured COX-1 and COX-2 mRNA expression by QPCR. High expression was defined as greater than or equal to median values. Clinical characteristics and disease outcomes were ascertained from medical records. Associations with disease-free survival (DFS) and overall survival (OS) were quantified by hazard ratios (HRs) and confidence intervals (CIs) from proportional hazards regression.

resultsType I tumors had high COX-2 expression, while type II tumors had high COX-1 expression. In multivariable adjusted regression models, higher COX-1 mRNA expression was associated with shorter DFS (HR: 6.37, 95% CI: 1.84-22.01) and OS (HR: 2.26, 95% CI: 1.04-4.91), while higher H-scores for COX-2 expression were associated with shorter DFS (HR: 1.92, 95% CI: 1.06-3.49). Stratified analysis indicated that COX-2 was significantly associated with DFS among cases with Type II tumors (HR: 1.93, 95% CI: 1.06-3.53).

conclusionsThese findings suggest that ovarian tumor type contributes to differences in COX expression levels and associations with survival.

Indexed as

Biomarkers, TumorGene Expression Regulation, NeoplasticAgedCyclooxygenase 1Cyclooxygenase 2FemaleHumansImmunohistochemistryKaplan-Meier EstimateMiddle AgedNeoplasm GradingNeoplasm StagingOvarian NeoplasmsPrognosisProportional Hazards ModelsProstaglandin-Endoperoxide SynthasesBiomarkers, TumorCyclooxygenase 1Cyclooxygenase 2Prostaglandin-Endoperoxide SynthasesCyclooxygenaseOvarian cancerSurvival analysisTumor subtype

Identifiers

PMID29482584
PMCPMC5828488
OpenAlexW2796233267

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.