Evidence map›Paper›PMID 34927235›Full record

ArticleActa obstetricia et gynecologica Scandinavica2022

Cyclic activity of signal transduction pathways in fimbrial epithelium of the human fallopian tube.

Phyllis van der Ploeg, Aniek Uittenboogaard, Karlijn M M Bucks, Marjolein H F M Lentjes-Beer, Steven L Bosch, Minouche M E van Rumste, M Caroline Vos, Paul J van Diest, Sandrina Lambrechts, Anja van de Stolpe and 2 more

Abstract read
In one paragraph

Article in Acta obstetricia et gynecologica Scandinavica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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

12 authors.

Phyllis van der PloegDepartment of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, The Netherlands.ORCID https://orcid.org/0000-0002-5099-7473
Aniek UittenboogaardDepartment of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, The Netherlands.
Karlijn M M BucksDepartment of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, The Netherlands.
Marjolein H F M Lentjes-BeerLaboratory for Pathology and Medical Microbiology (Stichting PAMM), Eindhoven, The Netherlands.
Steven L BoschLaboratory for Pathology and Medical Microbiology (Stichting PAMM), Eindhoven, The Netherlands.
Minouche M E van RumsteDepartment of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, The Netherlands.
M Caroline VosDepartment of Obstetrics and Gynecology, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.
Paul J van DiestDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Sandrina LambrechtsDepartment of Obstetrics and Gynecology, Maastricht University Medical Center, Maastricht, The Netherlands.
Anja van de StolpeMolecular Pathway Dx, Philips, Eindhoven, The Netherlands.
Ruud L M BekkersDepartment of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, The Netherlands.
Jurgen M J PiekDepartment of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, The Netherlands.

Funding

Catharina Research fundMolecular Pathway Dx, Philips
6 · The paper itself

Abstract

introductionThe local environment of the fallopian tube represents the optimal conditions for reproductive processes. To maintain tissue homeostasis, signal transduction pathways are thought to play a pivotal role. Enhancing our understanding of functional signal transduction pathway activity is important to be able to clarify the role of aberrant signal transduction pathway activity leading to female subfertility and other tubal diseases. Therefore, in this study we investigate the influence of the hormonal cycle on the activity of key signal transduction pathways in the fimbrial epithelium of morphologically normal fallopian tubes. MATERIAL AND

methodsWe included healthy pre- (n = 17) and postmenopausal (n = 8) patients who had surgical interventions for benign gynecologic conditions. Histologic sections of the fallopian tubes were reviewed by two pathologists and, for the premenopausal patients, hormone serum levels and sections of the endometrium were examined to determine the hormonal phase (early follicular [n = 4], late follicular [n = 3], early luteal [n = 5], late luteal [n = 5]). After laser capture microdissection, total mRNA was extracted from the fimbrial epithelium and real-time quantitative reverse transcription-PCR was performed to determine functional signal transduction pathway activity of the androgen receptor (AR), estrogen receptor (ER), phosphoinositide-3-kinase (PI3K), Hedgehog (HH), transforming growth factor-beta (TGF-β) and canonical wingless-type MMTV integration site (Wnt) pathways.

resultsThe early luteal phase demonstrated high AR and ER pathway activity in comparison with the late luteal phase (p = 0.016 and p = 0.032, respectively) and low PI3K activity compared with the late follicular phase (p = 0.036), whereas the late luteal phase showed low activity of HH and Wnt compared with the early follicular phase (both p = 0.016). Signal transduction pathway activity in fimbrial epithelium from postmenopausal patients was most similar to the early follicular and/or late luteal phase with regard to the AR, ER and PI3K pathways. Wnt pathway activity in postmenopausal patients was comparable to the late follicular and early luteal phase. We observed no differences in HH and TGF-β pathway activity between pre- and postmenopausal samples. The cyclic changes in signal transduction pathway activity suggest a stage-specific function which may affect the morphology and physiology of the human fallopian tube.

conclusionsWe demonstrated cyclic changes in activity of the AR, ER, PI3K, HH and Wnt pathways throughout the hormonal cycle.

Indexed as

MenopauseAgedEpitheliumFallopian TubesFemaleHedgehog ProteinsHumansMenstrual CycleMiddle AgedReceptors, AndrogenReceptors, EstrogenReceptors, WntReference ValuesReverse Transcriptase Polymerase Chain ReactionSignal TransductionHedgehog ProteinsReceptors, AndrogenReceptors, EstrogenReceptors, Wntcomputational modelsfimbriaehormonal cyclehuman fallopian tubesignal transduction pathways

Identifiers

PMID34927235
PMCPMC9564698

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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.