Evidence map›Paper›PMID 40076861›Full record

ArticleInternational journal of molecular sciences2025

Determining Sex-Specific Gene Expression Differences in Human Chorion Trophoblast Cells.

Daphne D Arena Goncharov, Ryan C V Lintao, Rheanna Urrabaz-Garza, Enkhtuya Radnaa, Ananth K Kammala, Lauren S Richardson, Ramkumar Menon

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Daphne D Arena GoncharovDivision of Basic Science and Translational Research, The University of Texas Medical Branch, Galveston, TX 77555, USA.
Ryan C V LintaoDivision of Basic Science and Translational Research, The University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0001-7192-2377
Rheanna Urrabaz-GarzaDivision of Basic Science and Translational Research, The University of Texas Medical Branch, Galveston, TX 77555, USA.
Enkhtuya RadnaaDivision of Basic Science and Translational Research, The University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0001-8142-8137
Ananth K KammalaDivision of Basic Science and Translational Research, The University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0001-5300-2083
Lauren S RichardsonDivision of Basic Science and Translational Research, The University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0001-8392-2833
Ramkumar MenonDivision of Basic Science and Translational Research, The University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0001-9213-6105

Funding

Developing extracellular vesicle based therapeutics against pre-term birth through the use of maternal-fetal interface on a chipUG3TR003283 · NCATS · TEXAS ENGINEERING EXPERIMENT STATION · PI HAN, ARUM, MENON, RAMKUMAR · 2020 to 2021
$1.5M
Investigating the molecular mechanism of P-gp/NHERF-1 network at feto maternal interface and role of paracrine signaling of EVs containing drug transporter proteinsR01HD113193 · NICHD · UNIVERSITY OF TEXAS MED BR GALVESTON · PI KAMMALA, ANANTH KUMAR · 2023 to 2025
$914k
NCATS NIH HHS UG3 TR003283NICHD NIH HHS R01 HD113193NIH HHS 1UG3TR003283-04A1
6 · The paper itself

Abstract

Differences in male (M) and female (F) neonates' premature birth outcomes and placental trophoblast inflammation have been observed but are unknown to occur within the fetal membrane trophoblast layer (chorion trophoblasts [CTC]). This study examined whether sex-based differences in gene expression and inflammatory marker expression can be observed in CTCs under control or infectious inflammatory conditions modeling preterm birth. CTCs from six different patient-derived fetal membrane samples (3M/3F) were cultured and divided into experimental (Lipopolysaccharide [LPS]) and control groups for 6, 12, or 24 h. RNA from CTCs was subjected to RNA-seq, while cytokine multiplex or ELISA detected pro-/anti-inflammatory cytokines, progesterone, and soluble HLA-G in cell supernatants. CTC-M and CTC-F showed sex, time, and stimulant-dependent differential gene expression profiles. Cytokine analysis demonstrated a significantly lower IL-6 production in control CTC-M than in CTC-F. No sex-dependent responses were observed after LPS treatment regarding cytokines. CTC-M produced significantly lower progesterone than CTC-F. The theories of sexual dimorphism linked to placental inflammation may not extend to CTCs. This study supports that the chorion acts as a "great wall" protecting the fetus by being refractory to insults. Further examination into the weaknesses of the chorion barrier and sex-dependent responses of fetal membranes is needed.

Indexed as

ChorionSex CharacteristicsTrophoblastsCytokinesFemaleGene Expression ProfilingGene Expression RegulationHumansLipopolysaccharidesMalePregnancyProgesteroneTranscriptomeCytokinesLipopolysaccharidesProgesteronechorionfemalefetal membranesinfectionmale

Identifiers

PMID40076861
PMCPMC11900912

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Registered trials

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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.