Evidence map›Paper›PMID 31658584›Full record

ArticleInternational journal of molecular sciences2019

Dysregulation of Placental Functions and Immune Pathways in Complete Hydatidiform Moles.

Jennifer R King, Melissa L Wilson, Szabolcs Hetey, Peter Kiraly, Koji Matsuo, Antonio V Castaneda, Eszter Toth, Tibor Krenacs, Petronella Hupuczi, Paulette Mhawech-Fauceglia and 7 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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.

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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Molecular Basis of Hydatidiform Moles-A Systematic Review.International journal of molecular sciences · 2024
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Derivation of human triploid trophoblast stem cells.Journal of assisted reproduction and genetics · 2022
    Article
  10. Article
  11. Review
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

17 authors.

Jennifer R KingDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. jennyrenaeking@gmail.com.
Melissa L WilsonDepartment of Preventive Medicine, University of Southern California, Los Angeles, CA 90033, USA. melisslw@usc.edu.ORCID 0000-0001-7785-4221
Szabolcs HeteySystems Biology of Reproduction Research Group, Institute of Enzymology, Research Centre for Natural Sciences, H-1117 Budapest, Hungary. heteysz@gmail.com.
Peter KiralySystems Biology of Reproduction Research Group, Institute of Enzymology, Research Centre for Natural Sciences, H-1117 Budapest, Hungary. peter0kiraly@gmail.com.
Koji MatsuoDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. koji.matsuo@med.usc.edu.ORCID 0000-0002-6232-8701
Antonio V CastanedaDepartment of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. antonio.castaneda@osumc.edu.
Eszter TothSystems Biology of Reproduction Research Group, Institute of Enzymology, Research Centre for Natural Sciences, H-1117 Budapest, Hungary. toth.eszter@ttk.hu.ORCID 0000-0001-7149-1482
Tibor KrenacsFirst Department of Pathology and Experimental Cancer Research, Semmelweis University, H-1085 Budapest, Hungary. krenacst@gmail.com.ORCID 0000-0001-9164-065X
Petronella HupucziMaternity Private Clinic of Obstetrics and Gynecology, H-1126 Budapest, Hungary. hupuczi.petronella@maternity.hu.
Paulette Mhawech-FaucegliaDepartment of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. pfauceglia@hotmail.com.
Andrea BaloghSystems Biology of Reproduction Research Group, Institute of Enzymology, Research Centre for Natural Sciences, H-1117 Budapest, Hungary. balogh.andrea@ttk.hu.ORCID 0000-0003-0322-1522
Andras SzilagyiSystems Biology of Reproduction Research Group, Institute of Enzymology, Research Centre for Natural Sciences, H-1117 Budapest, Hungary. szilagyi.andras@ttk.hu.ORCID 0000-0002-1773-6861
Janos MatkoDepartment of Immunology, Institute of Biology, Eotvos Lorand University, H-1117 Budapest, Hungary. matko@elte.hu.ORCID 0000-0001-9434-934X
Zoltan PappMaternity Private Clinic of Obstetrics and Gynecology, H-1126 Budapest, Hungary. pzorvosihetilap@maternity.hu.ORCID 0000-0002-7532-9703
Lynda D RomanDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. lroman@usc.edu.ORCID 0000-0002-6960-4414
Victoria K CortessisDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. victoria.cortessis@med.usc.edu.ORCID 0000-0002-2339-1089
Nandor Gabor ThanDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. than.gabor@ttk.hu.ORCID 0000-0001-9385-7019

Funding

Gynecologic Oncology Research Fund USCHungarian Ministry for National Economy VEKOP-2.3.3-15-2017-0014Hungarian National Research, Development and Innovation Office FIEK_16-1-2016-0005Hungarian Scientific Research Fund K124862Hungarian Scientific Research Fund K128262Magyar Tudományos Akadémia Medinprot Protein Science Research Synergy IV and Adhoc Program grantsMagyar Tudományos Akadémia Momentum LP2014-7/2014Magyar Tudományos Akadémia Premium_2019-436 grantMagyar Tudományos Akadémia Young Research Fellowships
6 · The paper itself

Abstract

Gene expression studies of molar pregnancy have been limited to a small number of candidate loci. We analyzed high-dimensional RNA and protein data to characterize molecular features of complete hydatidiform moles (CHMs) and corresponding pathologic pathways. CHMs and first trimester placentas were collected, histopathologically examined, then flash-frozen or paraffin-embedded. Frozen CHMs and control placentas were subjected to RNA-Seq, with resulting data and published placental RNA-Seq data subjected to bioinformatics analyses. Paraffin-embedded tissues from CHMs and control placentas were used for tissue microarray (TMA) construction, immunohistochemistry, and immunoscoring for galectin-14. Of the 14,022 protein-coding genes expressed in all samples, 3,729 were differentially expressed (DE) in CHMs, of which 72% were up-regulated. DE genes were enriched in placenta-specific genes (OR = 1.88,

Indexed as

ChoriocarcinomaCytokinesDNA MethylationDown-RegulationFemaleGene ExpressionGestational Trophoblastic DiseaseHumansHydatidiform MoleImmunohistochemistryPlacentaPregnancyPregnancy Trimester, FirstSystems BiologyUp-RegulationCytokineschoriocarcinomagalectingestational trophoblastic diseasehydatidiform moleplacental-specific genesystems biologytrophoblast differentiation

Identifiers

PMID31658584
PMCPMC6829352

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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.