Evidence map›Paper›PMID 23934194›Full record

ReviewOncogene2014

Epithelial ovarian cancer experimental models.

E Lengyel, J E Burdette, H A Kenny, D Matei, J Pilrose, P Haluska, K P Nephew, D B Hales, M S Stack

Abstract readReview
In one paragraph

Review in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers.

0numbers the graph read from it
0cells of the map it votes in
134citing 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

134 citing papers in PubMed.

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  10. The Prognostic Value of the Hedgehog Signaling Pathway in Ovarian Cancer.International journal of molecular sciences · 2025
    Article
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  16. Review
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  20. Exploiting a living biobank to delineate mechanisms underlying disease-specific chromosome instability.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2023
    Review

74 more citing papers are in PubMed but not listed here.

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.

E LengyelSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Chicago, Chicago, IL, USA.
J E BurdetteDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois/Chicago, Chicago, IL, USA.
H A KennySection of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Chicago, Chicago, IL, USA.
D MateiDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
J PilroseMedical Sciences, Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Bloomington, IN, USA.
P HaluskaDivision of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
K P NephewMedical Sciences, Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Bloomington, IN, USA.
D B HalesDepartment of Physiology, Southern Illinois University, Carbondale, IL, USA.
M S StackDepartment of Chemistry and Biochemistry, Harper Cancer Research Institute, University of Notre Dame, South Bend, IN, USA.

Funding

Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
Receptor Cross-Talk in Early Metastatic DisseminationR01CA109545 · NCI · UNIVERSITY OF NOTRE DAME · PI STACK, MARY SHARON · 2006 to 2022
$4.3M
REGULATION OF OVARIAN CARCINOMA PROTEINASESR01CA086984 · NCI · UNIVERSITY OF NOTRE DAME · PI STACK, MARY SHARON · 2000 to 2014
$3.8M
Regulation of Adhesion and Proteolysis in Ovarian CancerR01CA111882 · NCI · UNIVERSITY OF CHICAGO · PI LENGYEL, ERNST · 2006 to 2016
$2.8M
DNA Methylation and Ovarian CancerR01CA085289 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI NEPHEW, KENNETH P · 2002 to 2012
$2.4M
Therapeutic Efficacy of Flaxseed in the Treatment of Ovarian CancerR01AT005295 · NCCIH · SOUTHERN ILLINOIS UNIVERSITY CARBONDALE · PI HALES, DALE B · 2011 to 2015
$1.8M
Metabolic changes in ovarian cancer cells initiated by metastasis to adipose tissR01CA169604 · NCI · UNIVERSITY OF CHICAGO · PI LENGYEL, ERNST · 2013 to 2017
$1.7M
Dietary Intervention in the Gallus Domesticus Model of Ovarian CancerR03CA133915 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HALES, DALE B · 2008 to 2009
$160k
NCCIH NIH HHS AT00408NCCIH NIH HHS AT005295NCCIH NIH HHS R01 AT005295NCI NIH HHS CA085289NCI NIH HHS CA086984NCI NIH HHS CA109545NCI NIH HHS CA1113001NCI NIH HHS CA111882NCI NIH HHS CA133915NCI NIH HHS CA136393NCI NIH HHS P50 CA136393NCI NIH HHS R01 CA085289NCI NIH HHS R01 CA086984NCI NIH HHS R01 CA109545NCI NIH HHS R01 CA111882NCI NIH HHS R01 CA169604NCI NIH HHS R03 CA133915
6 · The paper itself

Abstract

Epithelial ovarian cancer (OvCa) is associated with high mortality and, as the majority (>75%) of women with OvCa have metastatic disease at the time of diagnosis, rates of survival have not changed appreciably over 30 years. A mechanistic understanding of OvCa initiation and progression is hindered by the complexity of genetic and/or environmental initiating events and lack of clarity regarding the cell(s) or tissue(s) of origin. Metastasis of OvCa involves direct extension or exfoliation of cells and cellular aggregates into the peritoneal cavity, survival of matrix-detached cells in a complex ascites fluid phase and subsequent adhesion to the mesothelium lining covering abdominal organs to establish secondary lesions containing host stromal and inflammatory components. Development of experimental models to recapitulate this unique mechanism of metastasis presents a remarkable scientific challenge, and many approaches used to study other solid tumors (for example, lung, colon and breast) are not transferable to OvCa research given the distinct metastasis pattern and unique tumor microenvironment (TME). This review will discuss recent progress in the development and refinement of experimental models to study OvCa. Novel cellular, three-dimensional organotypic, and ex vivo models are considered and the current in vivo models summarized. The review critically evaluates currently available genetic mouse models of OvCa, the emergence of xenopatients and the utility of the hen model to study OvCa prevention, tumorigenesis, metastasis and chemoresistance. As these new approaches more accurately recapitulate the complex TME, it is predicted that new opportunities for enhanced understanding of disease progression, metastasis and therapeutic response will emerge.

Indexed as

Models, BiologicalNeoplasms, Glandular and EpithelialOvarian NeoplasmsAnimalsAnimals, Genetically ModifiedCarcinoma, Ovarian EpithelialCell Line, TumorCell Transformation, NeoplasticHumansTumor Microenvironment

Identifiers

PMID23934194
PMCPMC3990646

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Registered trials

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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.