Evidence map›Paper›PMID 33068876›Full record

Trial reportPregnancy hypertension2020

Differential regulation of a placental SAM68 and sFLT1 gene pathway and the relevance to maternal vitamin D sufficiency.

Oyindamola Awe, James M Sinkway, Rebecca P Chow, Quentell Wagener, Elizabeth V Schulz, Jeremy Y Yu, Paul J Nietert, Carol L Wagner, Kyu-Ho Lee

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Pregnancy hypertension, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Role of Sam68 in different types of cancer (Review).International journal of molecular medicine · 2025
    Review
  4. Article
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

9 authors at 1 institution in 1 country.

Oyindamola AweDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC 29425, United States.
James M SinkwayDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC 29425, United States.
Rebecca P ChowDepartment of Medicine, Medical University of South Carolina, Charleston, SC 29425, United States.
Quentell WagenerDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC 29425, United States.
Elizabeth V SchulzDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC 29425, United States.
Jeremy Y YuDepartment of Medicine, Medical University of South Carolina, Charleston, SC 29425, United States.
Paul J NietertDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC 29425, United States.
Carol L WagnerDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC 29425, United States.
Kyu-Ho LeeDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC 29425, United States; Regenerative Medicine and Cell Biology Department, Medical University of South Carolina, Charleston, SC 29425, United States; Department of Obstetrics and Gynecology, Medical University of South Carolina, Charleston, SC 29425, United States. Electronic address: leekh@musc.edu.
Medical University of South Carolina · US

Funding

Subproject Title: Clinical Research Education, Mentoring and Career Development CoreU54GM104941 · NIGMS · UNIVERSITY OF DELAWARE · PI Gregory E Hicks · 2013 to 2026
$60.5M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
UBIQUITIN CARBOXYL TERMINAL HYDROLASE L1 (UCH-L1) AND VASCULAR LESION FORMATIONP20RR016434 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 2001 to 2011
$24.8M
Translational Research in Pediatric and Obstetric Pharmacology and TherapeuticsR01HD096501 · NICHD · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, JEREMY YONGXIN · 2018 to 2022
$2.0M
South Carolina Clinical & Translational Research Institute (SCTR)TL1TR000061 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2012 to 2014
$483k
NCATS NIH HHS TL1 TR000061NCATS NIH HHS UL1 TR001450NCRR NIH HHS P20 RR016434NICHD NIH HHS R01 HD096501NIGMS NIH HHS U54 GM104941
6 · The paper itself

Abstract

objectiveThe goal of this study was to determine if an axis of placental gene expression associated with early onset and severe preeclampsia (EOSPE) was operative in term pregnancy and correlated with vitamin D sufficiency.

methodsqPCR analysis of NKX2-5, SAM68, sFLT1 and membrane bound VEGFR1/FLT1 mRNA expression was conducted in placentas from 43 subjects enrolled in a vitamin D3 pregnancy supplementation trial. Pair-wise rank order correlations between patient-specific gene expression levels were calculated, and their relationship to maternal 25(OH)D status was assessed by a two-sample Wilcoxon test. Additionally, we probed the mechanistic link between SAM68 and sFLT1 using siRNA depletion in a human trophoblast cell line model.

resultsPositive and highly significant correlations were found between SAM68 vs. sFLT1 and SAM68 vs. FLT1 expression levels, as were significant and differential correlations between the expression of these genes and perinatal 25(OH)D status. The variability when stratified by race/ethnicity was qualitatively distinct from those previously observed in EOSPE. Mechanistic studies confirmed a functional role for SAM68 protein in the regulation of sFLT1 expression. NKX2-5 expression was not significantly correlated with sFLT1 or SAM68 expression in these samples, suggesting that its expression may be significant at earlier stages of pregnancy or be restricted to pathological settings.

conclusionsThese data further support our overarching hypothesis that SAM68 expression is a key determinant of VEGFR1 isoform expression in the placenta, and provide additional insights into how this gene pathway may be differentially deployed or modified in normal and pathological pregnancies.

Indexed as

Adaptor Proteins, Signal TransducingAdultCells, CulturedDNA-Binding ProteinsDNA, ComplementaryFemaleGene ExpressionHumansPlacentaPre-EclampsiaPregnancyRNA-Binding ProteinsVascular Endothelial Growth Factor Receptor-1Vitamin DAdaptor Proteins, Signal TransducingDNA-Binding ProteinsDNA, ComplementaryFLT1 protein, humanKHDRBS1 protein, humanRNA-Binding ProteinsVascular Endothelial Growth Factor Receptor-1Vitamin DNKX2-5PreeclampsiaPregnancySAM68sFLT1

Identifiers

PMID33068876
PMCPMC7688503
OpenAlexW3086196590

What OpenQuestion holds

Textmetadata
LicenceTDM
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.