Evidence map›Paper›PMID 25180169›Full record

ReviewRedox biology2014

Innate immunity and cell death in alcoholic liver disease: role of cytochrome P4502E1.

Mark A Barnes, Sanjoy Roychowdhury, Laura E Nagy

Open access · goldAbstract readReview
In one paragraph

Review in Redox biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. ProbioticFrontiers in microbiology · 2022
    Article
  10. The Immune System through the Lens of Alcohol Intake and Gut Microbiota.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Alcoholic Hepatitis: Lost in Translation.Journal of clinical and translational hepatology · 2018
    Review
  20. 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

3 authors at 1 institution in 1 country.

Mark A BarnesDepartment of Molecular Medicine, Case Western Reserve University, Cleveland, OH, United States ; Center for Liver Disease Research, Department of Pathobiology, Cleveland Clinic, Cleveland, OH, United States.
Sanjoy RoychowdhuryCenter for Liver Disease Research, Department of Pathobiology, Cleveland Clinic, Cleveland, OH, United States.
Laura E NagyDepartment of Molecular Medicine, Case Western Reserve University, Cleveland, OH, United States ; Center for Liver Disease Research, Department of Pathobiology, Cleveland Clinic, Cleveland, OH, United States ; Department of Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, OH, United States.
Cleveland Clinic · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024989 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI DAVIS, PAMELA B · 2007 to 2011
$53.7M
Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Role of Adipose in Ethanol-Induced Tissue InjuryR37AA011876 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2009 to 2018
$4.0M
Pilot ProjectP20AA017837 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2009 to 2013
$2.2M
MIF in progression and treatment of ALDU01AA020821 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2012 to 2016
$2.1M
RIP3-mediated necroptosis and ethanol-induced liver injuryR21AA020941 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI ROYCHOWDHURY, SANJOY · 2013 to 2014
$410k
NCATS NIH HHS UL1 TR000439NCRR NIH HHS UL1 RR024989NCRR NIH HHS UL1RR024989NIAAA NIH HHS 5U01AA020821NIAAA NIH HHS P20 AA017837NIAAA NIH HHS R21 AA020941NIAAA NIH HHS R21AA020941NIAAA NIH HHS R37 AA011876NIAAA NIH HHS R37AA011876NIAAA NIH HHS U01 AA020821
6 · The paper itself

Abstract

Ethanol-induced liver injury is a complex process dependent upon the interaction of multiple cell types in the liver, as well as activation of the innate immune response. Increased expression of CYP2E1 in response to high concentrations of ethanol leads to greater production of cytotoxic ethanol metabolites, which in turn contribute to production of reactive oxygen species, oxidative stress, and ultimately, cell death. Necroptotic hepatocyte cell death in response to ethanol is mediated via a CYP2E1-dependent expression of receptor-interacting protein kinase 3 (RIP3), a key component of the necroptosome. In response to alarmins released during ethanol-induced necroptosis, the innate immune response is activated. Macrophage migration inhibitory factor (MIF), a pro-inflammatory multikine involved in many disease processes, is an essential component to this response to injury. MIF expression is increased during ethanol exposure via a CYP2E1-dependent pathway, likely contributing to an exacerbated innate immune response and chronic inflammation after chronic ethanol. This review will discuss the complex interactions between CYP2E1-dependent expression of RIP3 and MIF in the pathophysiology of chronic ethanol-induced liver injury.

Indexed as

AnimalsCell DeathCytochrome P-450 CYP2E1EthanolHumansImmunity, InnateLiver Diseases, AlcoholicCytochrome P-450 CYP2E1EthanolAlcoholic liver diseaseCell deathChemokinesInnate immunityNecroptosis

Identifiers

PMID25180169
PMCPMC4143810
OpenAlexW2009835065

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.