Evidence map›Paper›PMID 26879975›Full record

ArticleJournal of ovarian research2016

Genome-wide transcriptional regulation of estrogen receptor targets in fallopian tube cells and the role of selective estrogen receptor modulators.

Georgette Moyle-Heyrman, Matthew J Schipma, Matthew Dean, David A Davis, Joanna E Burdette

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.2field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  12. Active Estrogen Receptor-alpha Signaling in Ovarian Cancer Models and Clinical Specimens.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
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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

5 authors at 3 institutions in 1 country.

Georgette Moyle-HeyrmanDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, Illinois, 60607, USA. georgette.heyrman@gmail.com.
Matthew J SchipmaNext Generation Sequencing Core Facility, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, 60611, USA. m-schipma@northwestern.edu.
Matthew DeanDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, Illinois, 60607, USA. mjdean@uic.edu.
David A DavisDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, Illinois, 60607, USA. davisda@uic.edu.
Joanna E BurdetteDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, Illinois, 60607, USA. joannab@uic.edu.
University of Illinois Chicago · USNorthwestern University · USUniversity of Wisconsin–Green Bay · US

Funding

Ex Vivo Female Reproductive Tract Integration In a 3D Microphysiologic SystemUH3TR001207 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WOODRUFF, TERESA K · 2014 to 2016
$4.9M
Steroid-Based Contrast Agents for Magnetic Resonance Imaging of Endocrine DiseaseR01EB014806 · NIBIB · NORTHWESTERN UNIVERSITY · PI MEADE, THOMAS J · 2012 to 2015
$1.4M
NCATS NIH HHS UH3 TR001207NIBIB NIH HHS R01 EB014806
6 · The paper itself

Abstract

backgroundThe fallopian tube epithelium is one of the potential sources of high-grade serous ovarian cancer (HGSC). The use of estrogen only hormone replacement therapy increases ovarian cancer (OVCA) risk. Despite estrogen's influence in OVCA, selective estrogen receptor modulators (SERMs) typically demonstrate only a 20 % response rate. This low response could be due to a variety of factors including the loss of estrogen receptor signaling or the role of estrogen in different potential cell types of origin. The response of fallopian tube epithelium to SERMs is not known, and would be useful when determining therapeutic options for tumors arising from this cell type, such as HGSC.

resultsUsing normal murine derived oviductal epithelial cells (mouse equivalent to the fallopian tube) estrogen receptor expression was confirmed and interaction with its ligand, estradiol, triggered mRNA and protein induction of progesterone receptor (PR). The SERMs 4-hydroxytamoxifen, raloxifene and desmethylarzoxifene, functioned as estrogen receptor antagonists in oviductal cells. Cellular proliferation and migration assays suggested that estradiol does not significantly impact cellular migration and increased proliferation. Further, using RNAseq, the oviduct specific transcriptional genes targets of ER when stimulated by estradiol and 4-hydroxytamoxifen signaling were determined and validated. The RNA-seq revealed enrichment in proliferation, anti-apoptosis, calcium signaling and steroid signaling processes. Finally, the ER and PR receptor status of a panel of HGSC cell lines was investigated including Kuramochi, OVSAHO, OVKATE, OVCAR3, and OVCAR4. OVSAHO demonstrated receptor expression and response, which highlights the need for additional models of ovarian cancer that are estrogen responsive.

conclusionsOverall, the fallopian tube has specific gene targets of estrogen receptor and demonstrates a tissue specific response to SERMs consistent with antagonistic action.

Indexed as

TranscriptomeAnimalsAntineoplastic Agents, HormonalCarcinoma in SituCell Line, TumorDrug Resistance, NeoplasmEstradiolEstrogen AntagonistsEstrogensFallopian TubesFemaleGene Expression Regulation, NeoplasticGenomeHumansMiceNeoplasms, Cystic, Mucinous, and SerousafimoxifeneAntineoplastic Agents, HormonaldesmethylarzoxifeneEstradiolEstrogen AntagonistsEstrogensPiperidinesRaloxifene HydrochlorideReceptors, EstrogenTamoxifenThiophenes

Identifiers

PMID26879975
PMCPMC4754840
OpenAlexW2280263946

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.