Evidence map›Paper›PMID 24388745›Full record

ArticleCell reports2014

S-nitrosothiol signaling regulates liver development and improves outcome following toxic liver injury.

Andrew G Cox, Diane C Saunders, Peter B Kelsey, Allie A Conway, Yevgenia Tesmenitsky, Julio F Marchini, Kristin K Brown, Jonathan S Stamler, Dorothy B Colagiovanni, Gary J Rosenthal and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 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
4.5field-weighted citation impact, top 6% 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, 49 citations in OpenAlex.

  1. Nitric Oxide Signaling and Sensing in Age-Related Diseases.Antioxidants (Basel, Switzerland) · 2024
    Review
  2. Article
  3. Using different zebrafish models to explore liver regeneration.Frontiers in cell and developmental biology · 2024
    Review
  4. Review
  5. Article
  6. The KEAP1-NRF2 pathway regulates TFEB/TFE3-dependent lysosomal biogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Update on Hepatobiliary Plasticity.Seminars in liver disease · 2023
    Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Increased GSNOR Expression during Aging Impairs Cognitive Function and Decreases S-Nitrosation of CaMKIIα.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  17. Review
  18. Article
  19. Review
  20. 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

13 authors at 6 institutions in 1 country.

Andrew G CoxGenetics Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Diane C SaundersGenetics Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Peter B KelseyGenetics Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Allie A ConwayGenetics Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Yevgenia TesmenitskyCardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Julio F MarchiniCardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Kristin K BrownDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.
Jonathan S StamlerInstitute for Transformative Molecular Medicine and Department of Medicine, Harrington Discovery Institute, Case Western Reserve University and University Hospitals Case Medical Center, Cleveland, OH 44106, USA.
Dorothy B ColagiovanniN30 Pharmaceuticals, Boulder, CO 80301, USA.
Gary J RosenthalN30 Pharmaceuticals, Boulder, CO 80301, USA.
Kevin J CroceCardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Trista E NorthDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Cambridge, MA 02138, USA. Electronic address: tnorth@bidmc.harvard.edu.
Wolfram GoesslingGenetics Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Cambridge, MA 02138, USA; Gastroenterology Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA; Gastrointestinal Cancer Center, Dana-Farber Cancer Institute, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. Electronic address: wgoessling@partners.org.
Brigham and Women's Hospital · USHarvard University · USNivalis Therapeutics (United States) · USBroad Institute · USCase Western Reserve University · USHarvard Stem Cell Institute · US

Funding

Estrogen Regulation of Hepatic GrowthR01DK090311 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI GOESSLING, WOLFRAM · 2011 to 2020
$4.9M
NIDDK NIH HHS DK090311NIDDK NIH HHS R01 DK090311
6 · The paper itself

Abstract

Toxic liver injury is a leading cause of liver failure and death because of the organ's inability to regenerate amidst massive cell death, and few therapeutic options exist. The mechanisms coordinating damage protection and repair are poorly understood. Here, we show that S-nitrosothiols regulate liver growth during development and after injury in vivo; in zebrafish, nitric-oxide (NO) enhanced liver formation independently of cGMP-mediated vasoactive effects. After acetaminophen (APAP) exposure, inhibition of the enzymatic regulator S-nitrosoglutathione reductase (GSNOR) minimized toxic liver damage, increased cell proliferation, and improved survival through sustained activation of the cytoprotective Nrf2 pathway. Preclinical studies of APAP injury in GSNOR-deficient mice confirmed conservation of hepatoprotective properties of S-nitrosothiol signaling across vertebrates; a GSNOR-specific inhibitor improved liver histology and acted with the approved therapy N-acetylcysteine to expand the therapeutic time window and improve outcome. These studies demonstrate that GSNOR inhibitors will be beneficial therapeutic candidates for treating liver injury.

Indexed as

AcetaminophenAldehyde OxidoreductasesAnimalsChemical and Drug Induced Liver InjuryLiverMiceMice, Inbred C57BLNF-E2-Related Factor 2Nitric OxideNitric Oxide DonorsS-NitrosothiolsZebrafishZebrafish ProteinsAcetaminophenAldehyde Oxidoreductasesformaldehyde dehydrogenase, glutathione-independentnfe2l2a protein, zebrafishNF-E2-Related Factor 2Nitric OxideNitric Oxide DonorsS-NitrosothiolsZebrafish Proteins

Identifiers

PMID24388745
PMCPMC4008725
OpenAlexW1979972069

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.