Evidence map›Paper›PMID 24503642›Full record

ArticleScientific reports2014

Uterine selection of human embryos at implantation.

Jan J Brosens, Madhuri S Salker, Gijs Teklenburg, Jaya Nautiyal, Scarlett Salter, Emma S Lucas, Jennifer H Steel, Mark Christian, Yi-Wah Chan, Carolien M Boomsma and 10 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 132 papers.

0numbers the graph read from it
0cells of the map it votes in
132citing 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.

NCT04865367 completednot on this mapstarted 2021, after this paper: background citation

To Investigate How Secreted-embryo-derived Trypsin Initiates, Maintains and Terminates Ca2+ (Intracellular Calcium) Signals in Uterine Epithelial Cells

TypeobservationalSponsorART Fertility Clinics LLCRan2021 to 2023Enrolled81ConditionsInfertility, Infertility, Female, AneuploidyArmsExposure to culture media
NCT06165367 narecruitingnot on this mapstarted 2024, after this paper: background citation

Impact of Hyaluronan-enriched Medium on Pregnancy Outcomes Following Euploid Blastocyst Transfers

TypeinterventionalSponsorART Fertility Clinics LLCRan2024 to 2026Enrolled783ConditionsInfertility, Implantation Rate, Clinical Pregnancy Rate, Live Birth RateArmsEmbryoGlue Medium
3 · Its place in the literature

Who cites it

132 citing papers in PubMed.

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  17. TRPV6 channel function is involved in endometrial epithelial cell CaCellular and molecular life sciences : CMLS · 2025
    Article
  18. Review
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  20. Review

72 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

20 authors.

Jan J BrosensDivision of Reproductive Health, Warwick Medical School, Clinical Sciences Research Laboratories, University Hospital, Coventry CV2 2DX, UK.
Madhuri S Salker1] Division of Reproductive Health, Warwick Medical School, Clinical Sciences Research Laboratories, University Hospital, Coventry CV2 2DX, UK [2] Institute of Reproductive and Developmental Biology, Imperial College London, Hammersmith Hospital, London W12 ONN, UK.
Gijs TeklenburgDepartment for Reproductive Medicine and Gynecology, University Medical Center Utrecht, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Jaya NautiyalInstitute of Reproductive and Developmental Biology, Imperial College London, Hammersmith Hospital, London W12 ONN, UK.
Scarlett SalterDivision of Reproductive Health, Warwick Medical School, Clinical Sciences Research Laboratories, University Hospital, Coventry CV2 2DX, UK.
Emma S LucasDivision of Reproductive Health, Warwick Medical School, Clinical Sciences Research Laboratories, University Hospital, Coventry CV2 2DX, UK.
Jennifer H SteelInstitute of Reproductive and Developmental Biology, Imperial College London, Hammersmith Hospital, London W12 ONN, UK.
Mark ChristianDivision of Reproductive Health, Warwick Medical School, Clinical Sciences Research Laboratories, University Hospital, Coventry CV2 2DX, UK.
Yi-Wah ChanWarwick Systems Biology Centre, University of Warwick, Coventry CV4 7AL, UK.
Carolien M BoomsmaDepartment for Reproductive Medicine and Gynecology, University Medical Center Utrecht, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Jonathan D MooreWarwick Systems Biology Centre, University of Warwick, Coventry CV4 7AL, UK.
Geraldine M HartshorneDivision of Reproductive Health, Warwick Medical School, Clinical Sciences Research Laboratories, University Hospital, Coventry CV2 2DX, UK.
Sandra SućurovićDepartment of Physiology and Immunology, Medical School, University of Rijeka, Braće Branchetta 20, 51000 Rijeka, Croatia.
Biserka Mulac-JericevicDepartment of Physiology and Immunology, Medical School, University of Rijeka, Braće Branchetta 20, 51000 Rijeka, Croatia.
Cobi J HeijnenDepartment for Reproductive Medicine and Gynecology, University Medical Center Utrecht, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Siobhan QuenbyDivision of Reproductive Health, Warwick Medical School, Clinical Sciences Research Laboratories, University Hospital, Coventry CV2 2DX, UK.
Marian J Groot KoerkampMolecular Cancer Research, University Medical Center Utrecht, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Frank C P HolstegeMolecular Cancer Research, University Medical Center Utrecht, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Anatoly ShmygolDivision of Reproductive Health, Warwick Medical School, Clinical Sciences Research Laboratories, University Hospital, Coventry CV2 2DX, UK.
Nick S Macklon1] Department for Reproductive Medicine and Gynecology, University Medical Center Utrecht, PO Box 85500, 3508 GA, Utrecht, The Netherlands [2] Division of Developmental Origins of Adult Diseases (DOHaD), University of Southampton, Coxford Road, Southampton SO16 5YA, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human embryos frequently harbor large-scale complex chromosomal errors that impede normal development. Affected embryos may fail to implant although many first breach the endometrial epithelium and embed in the decidualizing stroma before being rejected via mechanisms that are poorly understood. Here we show that developmentally impaired human embryos elicit an endoplasmic stress response in human decidual cells. A stress response was also evident upon in vivo exposure of mouse uteri to culture medium conditioned by low-quality human embryos. By contrast, signals emanating from developmentally competent embryos activated a focused gene network enriched in metabolic enzymes and implantation factors. We further show that trypsin, a serine protease released by pre-implantation embryos, elicits Ca(2+) signaling in endometrial epithelial cells. Competent human embryos triggered short-lived oscillatory Ca(2+) fluxes whereas low-quality embryos caused a heightened and prolonged Ca(2+) response. Thus, distinct positive and negative mechanisms contribute to active selection of human embryos at implantation.

Indexed as

AnimalsBlastocystCalcium SignalingCells, CulturedChromosome AberrationsCulture Media, ConditionedDeciduaEmbryo ImplantationEmbryo, MammalianEndoplasmic Reticulum StressEpithelial CellsFemaleGene Expression ProfilingHSC70 Heat-Shock ProteinsHumansInsulin-Like Growth Factor Binding Protein 1Culture Media, ConditionedHSC70 Heat-Shock ProteinsHSPA8 protein, humanIGFBP1 protein, humanInsulin-Like Growth Factor Binding Protein 1ProlactinRNA, Small InterferingTrypsin

Identifiers

PMID24503642
PMCPMC3915549

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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.