Evidence map›Paper›PMID 26008799›Full record

ArticleJournal of ovarian research2015

Expression and localisation of c-kit and KITL in the adult human ovary.

Astrud R Tuck, Rebecca L Robker, Robert J Norman, Wayne D Tilley, Theresa E Hickey

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2015. 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
4.6field-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, 37 citations in OpenAlex.

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  12. Parabens Accelerate Ovarian Dysfunction in a 4-Vinylcyclohexene Diepoxide-Induced Ovarian Failure Model.International journal of environmental research and public health · 2017
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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 1 institution in 2 countries.

Astrud R TuckRobinson Research Institute, School of Paediatrics and Reproductive Health, Adelaide, South Australia, Australia. astrud.tuck@adelaide.edu.au.
Rebecca L RobkerRobinson Research Institute, School of Paediatrics and Reproductive Health, Adelaide, South Australia, Australia. rebecca.robker@adelaide.edu.au.
Robert J NormanRobinson Research Institute, School of Paediatrics and Reproductive Health, Adelaide, South Australia, Australia. robert.norman@adelaide.edu.au.
Wayne D TilleyDame Roma Mitchell Cancer Research Laboratories, School of Medicine; University of Adelaide, Adelaide, South Australia, Australia. wayne.tilley@adelaide.edu.au.
Theresa E HickeyRobinson Research Institute, School of Paediatrics and Reproductive Health, Adelaide, South Australia, Australia. theresa.hickey@adelaide.edu.au.
USA Mitchell Cancer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe c-kit/kit ligand (KITL) signalling axis is an essential component of ovarian folliculogenesis in mammals, but little is known about expression and localisation of its key components in the ovaries of reproductive age women. This study aimed to characterise mRNA expression of c-kit and KITL isoforms and the localisation of c-kit and KITL proteins in adult human premenopausal ovaries.

methodsThis study utilised granulosa cells obtained from the preovulatory follicles of women undergoing assisted reproduction, pieces of ovarian tissue obtained from premenopausal women undergoing gynaecological surgeries and archival paraffin-embedded premenopausal ovarian tissues. Methodology included PCR for gene expression and Western blot or immunohistochemistry for protein expression.

resultsBoth c-kit mRNA isoforms, known as GNNK+ and GNNK-, were detected in human ovarian cortex, while KITL protein isoforms (KITL1 and KITL2) were present in ovarian cortex and human granulosa cells. Immunohistochemistry showed expression of KITL and c-kit protein in multiple cell types within follicles throughout development, from primordial follicles to large antral follicles, in addition to atretic follicles. Oocytes of all follicle stages expressed c-kit protein exclusively. Interestingly, unlike animal models, expression of both proteins displayed a less cell-type specific distribution with immunostaining present in granulosa, theca and stromal cells, suggesting that autocrine signalling occurs within the human ovary.

conclusionThe results of this study indicate that c-kit/KITL signalling also occurs in the human ovary, as established in various animal models, and may involve previously unknown autocrine signalling.

Indexed as

AdultAutocrine CommunicationFemaleGene Expression Regulation, NeoplasticGranulosa CellsHumansOocytesOvarian FollicleOvaryProto-Oncogene Proteins c-kitRNA, MessengerStem Cell FactorProto-Oncogene Proteins c-kitRNA, MessengerStem Cell Factor

Identifiers

PMID26008799
PMCPMC4460643
OpenAlexW2112516479

What OpenQuestion holds

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LicenceCC BY
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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.