Evidence map›Paper›PMID 24373743›Full record

ArticleMatrix biology : journal of the International Society for Matrix Biology2014

Biglycan and decorin differentially regulate signaling in the fetal membranes.

Zhiping Wu, Casie E Horgan, Olivia Carr, Rick T Owens, Renato V Iozzo, Beatrice E Lechner

Open access · hybridAbstract read
In one paragraph

Article in Matrix biology : journal of the International Society for Matrix Biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Novel regulatory roles of small leucine-rich proteoglycans in remodeling of the uterine cervix in pregnancy.Matrix biology : journal of the International Society for Matrix Biology · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Decorin is a devouring proteoglycan: Remodeling of intracellular catabolism via autophagy and mitophagy.Matrix biology : journal of the International Society for Matrix Biology · 2019
    Review
  14. Article
  15. Article
  16. Decorin interacting network: A comprehensive analysis of decorin-binding partners and their versatile functions.Matrix biology : journal of the International Society for Matrix Biology · 2016
    Review
  17. Agonists and Antagonists of TGF-β Family Ligands.Cold Spring Harbor perspectives in biology · 2016
    Review
  18. Review
  19. Decorin is an autophagy-inducible proteoglycan and is required for proper in vivo autophagy.Matrix biology : journal of the International Society for Matrix Biology · 2015
    Article
  20. Proteoglycans regulate autophagy via outside-in signaling: an emerging new concept.Matrix biology : journal of the International Society for Matrix Biology · 2015
    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

6 authors at 4 institutions in 1 country.

Zhiping WuDepartment of Pediatrics, Women and Infants Hospital of Rhode Island, The Warren Alpert Medical School of Brown University, 101 Dudley Street, Providence, RI 02905, USA.
Casie E HorganDepartment of Pediatrics, Women and Infants Hospital of Rhode Island, The Warren Alpert Medical School of Brown University, 101 Dudley Street, Providence, RI 02905, USA.
Olivia CarrDepartment of Pediatrics, Women and Infants Hospital of Rhode Island, The Warren Alpert Medical School of Brown University, 101 Dudley Street, Providence, RI 02905, USA.
Rick T OwensLifecell Corporation, 1 Millennium Way, Branchburg, NJ 08876, USA.
Renato V IozzoDepartment of Pathology, Anatomy & Cell Biology, Thomas Jefferson University, 1020 Locust Street, Philadelphia, PA 19107, USA.
Beatrice E LechnerDepartment of Pediatrics, Women and Infants Hospital of Rhode Island, The Warren Alpert Medical School of Brown University, 101 Dudley Street, Providence, RI 02905, USA. Electronic address: blechner@wihri.org.
Brown University · USMillennium Engineering and Integration (United States) · USThomas Jefferson University · USWomen & Infants Hospital of Rhode Island · US

Funding

NEOPLASTIC MODULATION OF PROTEOGLYCAN METABOLISMR01CA039481 · NCI · UNIVERSITY OF PENNSYLVANIA · PI IOZZO, RENATO V. · 1985 to 2020
$7.1M
The Biology of Perlecan in Cancer and AngiogenesisR01CA047282 · NCI · THOMAS JEFFERSON UNIVERSITY · PI IOZZO, RENATO V. · 1990 to 2019
$5.7M
COBRE for Perinatal BiologyP20GM103537 · NIGMS · WOMEN AND INFANTS HOSPITAL-RHODE ISLAND · PI PADBURY, JAMES F · 2012 to 2012
$2.1M
The Role of Biglycan in ReproductionK08HD054676 · NICHD · WOMEN AND INFANTS HOSPITAL-RHODE ISLAND · PI LECHNER, BEATRICE ELIZABETH · 2009 to 2013
$540k
NCI NIH HHS R01 CA039481NCI NIH HHS R01 CA047282NCI NIH HHS R01 CA39481NCI NIH HHS R01 CA47282NICHD NIH HHS 1K08HD054676NICHD NIH HHS K08 HD054676NIGMS NIH HHS P20 GM103537NIGMS NIH HHS P20GM12345
6 · The paper itself

Abstract

Preterm birth is the leading cause of newborn mortality in the United States and about one third of cases are caused by preterm premature rupture of fetal membranes, a complication that is frequently observed in patients with Ehlers-Danlos Syndrome. Notably, a subtype of Ehlers-Danlos Syndrome is caused by expression of abnormal biglycan and decorin proteoglycans. As compound deficiency of these two small leucine-rich proteoglycans is a model of preterm birth, we investigated the fetal membranes of Bgn(-/-); Dcn(-/-) double-null and single-null mice. Our results showed that biglycan signaling supported fetal membrane remodeling during early gestation in the absence of concomitant changes in TGFβ levels. In late gestation, biglycan signaling acted in a TGFβ-dependent manner to aid in membrane stabilization. In contrast, decorin signaling supported fetal membrane remodeling at early stages of gestation in a TGFβ-dependent manner, and fetal membrane stabilization at later stages of gestation without changes in TGFβ levels. Furthermore, exogenous soluble decorin was capable of rescuing the TGFβ signaling pathway in fetal membrane mesenchymal cells. Collectively, these findings provide novel targets for manipulation of fetal membrane extracellular matrix stability and could represent novel targets for research on preventive strategies for preterm premature rupture of fetal membranes.

Indexed as

Disease Models, AnimalAnalysis of VarianceAnimalsBiglycanBlotting, WesternCell Culture TechniquesDecorinDNA PrimersEhlers-Danlos SyndromeEnzyme-Linked Immunosorbent AssayExtraembryonic MembranesImmunohistochemistryMicePremature BirthSignal TransductionTransforming Growth Factor betaBgn protein, mouseBiglycanDcn protein, mouseDecorinDNA PrimersTransforming Growth Factor betaFetal membranesMMPSmadSmall leucine-rich proteoglycanTGF-βTIMP

Identifiers

PMID24373743
PMCPMC4039566
OpenAlexW1967540778

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.