Evidence map›Paper›PMID 26946093›Full record

ArticleGynecologic oncology2016

High expression of orphan nuclear receptor NR4A1 in a subset of ovarian tumors with worse outcome.

Evan Delgado, Michelle M Boisen, Robin Laskey, Rui Chen, Chi Song, Jad Sallit, Zachary A Yochum, Courtney L Andersen, Matthew J Sikora, Jacob Wagner and 8 more

Open access · greenAbstract read
In one paragraph

Article in Gynecologic oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

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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

18 authors at 9 institutions in 2 countries.

Evan DelgadoUniversity of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA.
Michelle M BoisenDivision of Gynecologic Oncology, Magee-Womens Hospital of the University of Pittsburgh Medical Center, Pittsburgh, PA, USA. Electronic address: boockmeiermm@mail.magee.edu.
Robin LaskeyDivision of Gynecologic Oncology, Magee-Womens Hospital of the University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Rui ChenDepartment of Biostatistics and Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, USA.
Chi SongDepartment of Biostatistics and Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, USA.
Jad SallitRoss University School of Medicine.
Zachary A YochumDepartment of Medicine, Division of Hematology Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
Courtney L AndersenDepartment of Pharmacology and Chemical Biology, Womens Cancer Research Center, Magee-Womens Research Institute, and University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA; Molecular Pharmacology Training Program, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Matthew J SikoraDepartment of Pharmacology and Chemical Biology, Womens Cancer Research Center, Magee-Womens Research Institute, and University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
Jacob WagnerUniversity of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA.
Stephen SafeDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, USA.
Esther ElishaevDepartment of Pathology, Magee-Womens Hospital of the University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Adrian LeeDepartment of Pharmacology and Chemical Biology, Womens Cancer Research Center, Magee-Womens Research Institute, and University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
Robert P EdwardsDivision of Gynecologic Oncology, Magee-Womens Hospital of the University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Paul HaluskaDepartment of Oncology and Pharmacology, Mayo Clinic, Rochester, MN, USA.
George TsengDepartment of Biostatistics and Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, USA.
Mark SchurdakUniversity of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA.
Steffi OesterreichDepartment of Pharmacology and Chemical Biology, Womens Cancer Research Center, Magee-Womens Research Institute, and University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
University of Pittsburgh · USMagee-Womens Hospital · USMagee-Womens Research Institute · USUniversity of Pittsburgh Medical Center · USUPMC Hillman Cancer Center · USDiscovery Institute · USMayo Clinic in Arizona · USRoss University School of Veterinary Medicine · KNTexas A&M University · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
PREDOCTORAL TRAINING IN PHARMACOLOGICAL SCIENCEST32GM008424 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PAGANO, PATRICK J · 1994 to 2019
$3.4M
NCI NIH HHS P30 CA047904NIGMS NIH HHS T32 GM008424
6 · The paper itself

Abstract

objectiveNuclear receptors (NRs) play a vital role in the development and progression of several cancers including breast and prostate. Using TCGA data, we sought to identify critical nuclear receptors in high grade serous ovarian cancers (HGSOC) and to confirm these findings using in vitro approaches.

methodsIn silico analysis of TCGA data was performed to identify relevant NRs in HGSOC. Ovarian cancer cell lines were screened for NR expression and functional studies were performed to determine the significance of these NRs in ovarian cancers. NR expression was analyzed in ovarian cancer tissue samples using immunohistochemistry to identify correlations with histology and stage of disease.

resultsThe NR4A family of NRs was identified as a potential driver of ovarian cancer pathogenesis. Overexpression of NR4A1 in particular correlated with worse progression free survival. Endogenous expression of NR4A1 in normal ovarian samples was relatively high compared to that of other tissue types, suggesting a unique role for this orphan receptor in the ovary. Expression of NR4A1 in HGSOC cell lines as well as in patient samples was variable. NR4A1 primarily localized to the nucleus in normal ovarian tissue while co-localization within the cytoplasm and nucleus was noted in ovarian cancer cell lines and patient tissues.

conclusionsNR4A1 is highly expressed in a subset of HGSOC samples from patients that have a worse progression free survival. Studies to target NR4A1 for therapeutic intervention should include HGSOC.

Indexed as

AnimalsCarcinoma, Ovarian EpithelialCell Line, TumorFemaleGenomeHeterograftsHumansImmunohistochemistryMiceMice, SCIDNeoplasms, Glandular and EpithelialNuclear Receptor Subfamily 4, Group A, Member 1Ovarian NeoplasmsPrognosisRNA, MessengerNR4A1 protein, humanNuclear Receptor Subfamily 4, Group A, Member 1RNA, MessengerNuclear receptorsOvarian cancerTherapeutic target

Identifiers

PMID26946093
PMCPMC5154956
OpenAlexW2296086222

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.