Evidence map›Paper›PMID 27939131›Full record

ArticleThe American journal of pathology2017

A Role for cAMP and Protein Kinase A in Experimental Necrotizing Enterocolitis.

Brian P Blackwood, Douglas R Wood, Carrie Yuan, Joseph Nicolas, Isabelle G De Plaen, Kathryn N Farrow, Pauline Chou, Jerrold R Turner, Catherine J Hunter

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Models of necrotizing enterocolitis.Seminars in perinatology · 2023
    Review
  7. Review
  8. Review
  9. Article
  10. Necrotizing Enterocolitis: Overview on In Vitro Models.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. 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

9 authors at 3 institutions in 1 country.

Brian P BlackwoodDivision of Pediatric Surgery, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Douglas R WoodDepartment of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Carrie YuanDepartment of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Joseph NicolasDepartment of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Isabelle G De PlaenDivision of Pediatric Surgery, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Kathryn N FarrowDivision of Pediatric Surgery, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Pauline ChouDivision of Pediatric Surgery, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
Jerrold R TurnerDepartments of Pathology and Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Catherine J HunterDivision of Pediatric Surgery, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois. Electronic address: chunter@luriechildrens.org.
Northwestern University · USLurie Children's Hospital · USBrigham and Women's Hospital · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
ZO-1-MEDIATED PROTEIN INTERACTIONS: REGULATORS AND INTEGRATORS OF DIVERSE EPITHELIAL FUNCTIONS IN HEALTH AND DISEASER01DK061931 · NIDDK · UNIVERSITY OF CHICAGO · PI JERROLD R. TURNER · 2001 to 2026
$15.0M
Therapeutic targeting of protein interactions to reverse MLCK1-mediated intestinal barrier loss and ameliorate disease.R01DK068271 · NIDDK · UNIVERSITY OF CHICAGO · PI JERROLD R. TURNER · 2005 to 2026
$11.3M
Translational Approaches to Develop Drug Therapy for DiarrheaR24DK099803 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI DONOWITZ, MARK · 2014 to 2019
$8.9M
Redox Regulation of Vascular cGMP Signaling in Neonatal LungsR01HL109478 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHUMACKER, PAUL T · 2011 to 2020
$4.2M
Defining bacterial virulence, cAMP and PKA in necrotizing enterocolitisK08DK106450 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI HUNTER, CATHERINE JANE · 2015 to 2021
$851k
NCI NIH HHS P30 CA060553NHLBI NIH HHS R01 HL109478NIDDK NIH HHS K08 DK106450NIDDK NIH HHS R01 DK068271NIDDK NIH HHS R24 DK099803
6 · The paper itself

Abstract

Necrotizing enterocolitis (NEC) is a devastating intestinal disease that has been associated with Cronobacter sakazakii and typically affects premature infants. Although NEC has been actively investigated, little is known about the mechanisms underlying the pathophysiology of epithelial injury and intestinal barrier damage. Cyclic adenosine monophosphate (cAMP) and protein kinase A (PKA) are important mediators and regulators of apoptosis. To test the hypothesis that C. sakazakii increases cAMP and PKA activation in experimental NEC resulting in increased epithelial apoptosis, we investigated the effects of C. sakazakii on cAMP and PKA in vitro and in vivo. Specifically, rat intestinal epithelial cells and a human intestinal epithelial cell line were infected with C. sakazakii, and cAMP levels and phosphorylation of PKA were measured. An increase in cAMP was demonstrated after infection, as well as an increase in phosphorylated PKA. Similarly, increased intestinal cAMP and PKA phosphorylation were demonstrated in a rat pup model of NEC. These increases were correlated with increased intestinal epithelial apoptosis. The additional of a PKA inhibitor (KT5720) significantly ameliorated these effects and decreased the severity of experimental NEC. Findings were compared with results from human tissue samples. Collectively, these observations indicate that cAMP and PKA phosphorylation are associated with increased apoptosis in NEC and that inhibition of PKA activation protects against apoptosis and experimental NEC.

Indexed as

AnimalsApoptosisBlotting, WesternCronobacter sakazakiiCyclic AMPCyclic AMP-Dependent Protein KinasesDisease Models, AnimalEnterocolitis, NecrotizingFemaleFlow CytometryFluorescent Antibody TechniqueHumansIntestinal MucosaPolymerase Chain ReactionRatsRats, Sprague-DawleyCyclic AMPCyclic AMP-Dependent Protein Kinases

Identifiers

PMID27939131
PMCPMC5389366
OpenAlexW2559876035

What OpenQuestion holds

Textmetadata
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.