Evidence map›Paper›PMID 31347667›Full record

ArticleBiology of reproduction2019

COX2 is induced in the ovarian epithelium during ovulatory wound repair and promotes cell survival†.

Lauren E Carter, David P Cook, Olga Collins, Lisa F Gamwell, Holly A Dempster, Howard W Wong, Curtis W McCloskey, Ken Garson, Nhung H Vuong, Barbara C Vanderhyden

Open access · greenAbstract read
In one paragraph

Article in Biology of reproduction, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  6. Common Analgesic Use for Menstrual Pain and Ovarian Cancer Risk.Cancer prevention research (Philadelphia, Pa.) · 2021
    Article
  7. 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

10 authors at 3 institutions in 1 country.

Lauren E CarterCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
David P CookCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Olga CollinsCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Lisa F GamwellCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Holly A DempsterCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Howard W WongCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Curtis W McCloskeyCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Ken GarsonCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Nhung H VuongCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Barbara C VanderhydenCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
University of Ottawa · CAOttawa Hospital · CAOttawa Hospital Research Institute

Funding

CIHR
6 · The paper itself

Abstract

The ovarian surface epithelium (OSE) is a monolayer of cells surrounding the ovary that is ruptured during ovulation. After ovulation, the wound is repaired, however, this process is poorly understood. In epithelial tissues, wound repair is mediated by an epithelial-to-mesenchymal transition (EMT). Transforming Growth Factor Beta-1 (TGFβ1) is a cytokine commonly known to induce an EMT and is present throughout the ovarian microenvironment. We, therefore, hypothesized that TGFβ1 induces an EMT in OSE cells and activates signaling pathways important for wound repair. Treating primary cultures of mouse OSE cells with TGFβ1 induced an EMT mediated by TGFβRI signaling. The transcription factor Snail was the only EMT-associated transcription factor increased by TGFβ1 and, when overexpressed, was shown to increase OSE cell migration. A polymerase chain reaction array of TGFβ signaling targets determined Cyclooxygenase-2 (Cox2) to be most highly induced by TGFβ1. Constitutive Cox2 expression modestly increased migration and robustly enhanced cell survival, under stress conditions similar to those observed during wound repair. The increase in Snail and Cox2 expression with TGFβ1 was reproduced in human OSE cultures, suggesting these responses are conserved between mouse and human. Finally, the induction of Cox2 expression in OSE cells during ovulatory wound repair was shown in vivo, suggesting TGFβ1 increases Cox2 to promote wound repair by enhancing cell survival. These data support that TGFβ1 promotes ovulatory wound repair by induction of an EMT and activation of a COX2-mediated pro-survival pathway. Understanding ovulatory wound repair may give insight into why ovulation is the primary non-hereditary risk factor for ovarian cancer.

Indexed as

Wound HealingAnimalsCell SurvivalCyclooxygenase 2DinoprostoneEnzyme-Linked Immunosorbent AssayFemaleGene Expression RegulationMiceOvarySnail Family Transcription FactorsTransforming Growth Factor beta1Cyclooxygenase 2DinoprostonePtgs2 protein, mouseSnail Family Transcription FactorsTransforming Growth Factor beta1Cyclooxygenase 2epithelial-to-mesenchymal transitionovarian surface epitheliumtransforming growth factor beta 1wound repair

Identifiers

PMID31347667
PMCPMC6877777
OpenAlexW2966193542

What OpenQuestion holds

Textmetadata
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.