Evidence map›Paper›PMID 32365902›Full record

ArticleInternational journal of molecular sciences2020

Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture Model.

Ramóna Pap, Gergely Montskó, Gergely Jánosa, Katalin Sipos, Gábor L Kovács, Edina Pandur

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Ramóna PapDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Pécs, H-7624 Rókus u. 2., Pécs, Hungary.
Gergely MontskóSzentágothai Research Centre, University of Pécs, H-7624 Ifjúság út 20., Pécs, Hungary.
Gergely JánosaDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Pécs, H-7624 Rókus u. 2., Pécs, Hungary.
Katalin SiposDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Pécs, H-7624 Rókus u. 2., Pécs, Hungary.ORCID 0000-0002-6706-2682
Gábor L KovácsSzentágothai Research Centre, University of Pécs, H-7624 Ifjúság út 20., Pécs, Hungary.
Edina PandurDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Pécs, H-7624 Rókus u. 2., Pécs, Hungary.ORCID 0000-0001-5012-3242
University of Pecs · HU

Funding

Economic Development and Innovation Operational Programme "The use of chip-technology in increasing the effectiveness of human in vitro fertilization" GINOP-2.3.2-15-2016-00021NRDI (OTKA) 115394/K
6 · The paper itself

Abstract

Embryo implantation is a complex process regulated by a network of biological molecules. Recently, it has been described that fractalkine (CX3CL1, FKN) might have an important role in the feto-maternal interaction during gestation since the trophoblast cells express fractalkine receptor (CX3CR1) and the endometrium cells secrete fractalkine. CX3CR1 controls three major signalling pathways, PLC-PKC pathway, PI3K/AKT/NFκB pathway and Ras-mitogen-activated protein kinases (MAPK) pathways regulating proliferation, growth, migration and apoptosis. In this study, we focused on the molecular mechanisms of FKN treatment influencing the expression of implantation-related genes in trophoblast cells (JEG-3) both in mono-and in co-culture models. Our results reveal that FKN acted in a concentration and time dependent manner on JEG-3 cells. FKN seemed to operate as a positive regulator of implantation via changing the action of progesterone receptor (PR), activin receptor and bone morphogenetic protein receptor (BMPR). FKN modified also the expression of matrix metalloproteinase 2 and 9 controlling invasion. The presence of HEC-1A endometrial cells in the co-culture contributed to the effect of fractalkine on JEG-3 cells regulating implantation. The results suggest that FKN may contribute to the successful attachment and implantation of embryo.

Indexed as

ActivinsBlotting, WesternBone Morphogenetic Protein 2Cell Line, TumorCell SurvivalChemokine CX3CL1Coculture TechniquesCX3C Chemokine Receptor 1FemaleFollistatinHumansImmunoblottingMAP Kinase Signaling Systemp38 Mitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesReal-Time Polymerase Chain ReactionActivinsBMP2 protein, humanBone Morphogenetic Protein 2Chemokine CX3CL1CX3C Chemokine Receptor 1CX3CR1 protein, humanFollistatinp38 Mitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesRNA, Messengerbilaminar co-cultureendometriumfractalkineimplantationtrophoblast

Identifiers

PMID32365902
PMCPMC7246682
OpenAlexW3021906757

What OpenQuestion holds

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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.