Evidence map›Paper›PMID 24324043›Full record

ArticleHypertension (Dallas, Tex. : 1979)2014

Excess LIGHT contributes to placental impairment, increased secretion of vasoactive factors, hypertension, and proteinuria in preeclampsia.

Wei Wang, Nicholas F Parchim, Takayuki Iriyama, Renna Luo, Cheng Zhao, Chen Liu, Roxanna A Irani, Weiru Zhang, Chen Ning, Yujin Zhang and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Review
  5. Article
  6. Article
  7. Review
  8. Vascular mechanisms and molecular targets in hypertensive pregnancy and preeclampsia.American journal of physiology. Heart and circulatory physiology · 2020
    Review
  9. Article
  10. Reciprocal upregulation of hypoxia-inducible factor-1α and persistently enhanced placental adenosine signaling contribute to the pathogenesis of preeclampsia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Matrix Metalloproteinases in Normal Pregnancy and Preeclampsia.Progress in molecular biology and translational science · 2017
    Review
  19. Article
  20. Preeclampsia and Pregnancy-Related Hypertensive Disorders.Hypertension (Dallas, Tex. : 1979) · 2016
    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

16 authors at 3 institutions in 2 countries.

Wei WangDepartment of Biochemistry and Molecular Biology, University of Texas Medical School at Houston, TX 77030. yang.xia@uth.tmc.edu.
Nicholas F Parchim
Takayuki Iriyama
Renna Luo
Cheng Zhao
Chen Liu
Roxanna A Irani
Weiru Zhang
Chen Ning
Yujin Zhang
Sean C Blackwell
Lieping Chen
Lijian Tao
M John Hicks
Rodney E Kellems
Yang Xia
University of Houston · USCentral South University · CNYale University · US

Funding

PURINE METABOLISM AT THE MATERNAL/FETAL INTERFACER01HD034130 · NICHD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KELLEMS, RODNEY E · 1996 to 2012
$2.8M
Autoantibodies in Preeclampsia: Pre-symptomatic markers and therapeutic targetsRC4HD067977 · NICHD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KELLEMS, RODNEY E, XIA, YANG · 2010 to 2010
$1.8M
Metabolites, Sickle Cell Disease, and Novel TherapeuticsR01HL113574 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIA, YANG · 2013 to 2016
$1.5M
Adenosine Signaling, Priapism and Sickle Cell DiseaseR01DK083559 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIA, YANG · 2009 to 2012
$1.3M
AT1 Receptor Activating Autoantibodies and PreeclampsiaR01HL076558 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIA, YANG · 2005 to 2008
$1.0M
Adenosine Signaling and PriapsimR21DK077748 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIA, YANG · 2007 to 2008
$405k
Angiotensin Receptor Autoantibodies and PreeclampsiaR56HD034130 · NICHD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KELLEMS, RODNEY E · 2007 to 2007
$371k
NHLBI NIH HHS R01 HL076558NHLBI NIH HHS R01 HL113574NICHD NIH HHS HD34130NICHD NIH HHS R01 HD034130NICHD NIH HHS R56 HD034130NICHD NIH HHS RC4 HD067977NICHD NIH HHS RC4HD067977NIDDK NIH HHS R01 DK083559NIDDK NIH HHS R21 DK077748
6 · The paper itself

Abstract

Preeclampsia, a prevalent hypertensive disorder of pregnancy, is believed to be secondary to uteroplacental ischemia. Accumulating evidence indicates that hypoxia-independent mediators, including inflammatory cytokines and growth factors, are associated with preeclampsia, but it is unclear whether these signals directly contribute to placental damage and disease development in vivo. We report that LIGHT, a novel tumor necrosis factor superfamily member, is significantly elevated in the circulation and placentas of preeclamptic women compared with normotensive pregnant women. Injection of LIGHT into pregnant mice induced placental apoptosis, small fetuses, and key features of preeclampsia, hypertension and proteinuria. Mechanistically, using neutralizing antibodies specific for LIGHT receptors, we found that LIGHT receptors herpes virus entry mediator and lymphotoxin β receptor are required for LIGHT-induced placental impairment, small fetuses, and preeclampsia features in pregnant mice. Accordingly, we further revealed that LIGHT functions through these 2 receptors to induce secretion of soluble fms-like tyrosine kinase-1 and endothelin-1, 2 well-accepted pathogenic factors in preeclampsia, and thereby plays an important role in hypertension and proteinuria in pregnant mice. Lastly, we extended our animal findings to human studies and demonstrated that activation of LIGHT receptors resulted in increased apoptosis and elevation of soluble fms-like tyrosine kinase-1 secretion in human placental villous explants. Overall, our human and mouse studies show that LIGHT signaling is a previously unrecognized pathway responsible for placental apoptosis, elevated secretion of vasoactive factors, and subsequent maternal features of preeclampsia, and reveal new therapeutic opportunities for the management of the disease.

Indexed as

Pregnancy, AnimalAdultAnimalsDisease Models, AnimalEndothelinsFemaleHumansMiceMice, Inbred C57BLPlacentaPre-EclampsiaPregnancyProteinuriaSignal TransductionTumor Necrosis Factor Ligand Superfamily Member 14EndothelinsTumor Necrosis Factor Ligand Superfamily Member 14endothelin-1herpes virus entry mediatorlymphotoxin-beta receptorpreeclampsiareceptors, tumor necrosis factor, member 14tumor necrosis factor ligand superfamily member 14

Identifiers

PMID24324043
PMCPMC4053533
OpenAlexW2108188095

What OpenQuestion holds

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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.