Evidence map›Paper›PMID 29637855›Full record

ReviewCurrent pharmaceutical design2018

Cytochrome P450s and Alcoholic Liver Disease.

Yongke Lu, Arthur I Cederbaum

Open access · greenAbstract readReview
In one paragraph

Review in Current pharmaceutical design, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

63 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Hepatoprotective effects of silybin in liver fibrosis.World journal of gastroenterology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Phenoconversion andHepatology forum · 2025
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Interaction between fatty acid oxidation and ethanol metabolism in liver.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Review
  19. FermentedJournal of microbiology and biotechnology · 2024
    Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Yongke LuDepartment of Health Sciences, College of Public Health, East Tennessee State University Johanson City, TN37614, United States.
Arthur I CederbaumDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, Newyork, United States.
East Tennessee State University · USIcahn School of Medicine at Mount Sinai · US

Funding

Nicotine and Alcoholic Liver DiseaseR01AA024723 · NIAAA · MARSHALL UNIVERSITY · PI LU, YONGKE · 2016 to 2020
$1.8M
Alcohol-Induced Fatty Liver and Injury in Humanized CYP2E1 Knockin Mice.R01AA018790 · NIAAA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CEDERBAUM, ARTHUR I · 2009 to 2011
$1.1M
CYP2A5 and alcoholic liver diseaseR21AA020877 · NIAAA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LU, YONGKE · 2013 to 2014
$438k
Role of autophagy on the modulation of CYP2E1 alcohol liver toxicityR21AA021362 · NIAAA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CEDERBAUM, ARTHUR I · 2012 to 2013
$431k
NIAAA NIH HHS R01 AA018790NIAAA NIH HHS R01 AA024723NIAAA NIH HHS R21 AA020877NIAAA NIH HHS R21 AA021362
6 · The paper itself

Abstract

Alcohol consumption causes liver diseases, designated as Alcoholic Liver Disease (ALD). Because alcohol is detoxified by alcohol dehydrogenase (ADH), a major ethanol metabolism system, the development of ALD was initially believed to be due to malnutrition caused by alcohol metabolism in liver. The discovery of the microsomal ethanol oxidizing system (MEOS) changed this dogma. Cytochrome P450 enzymes (CYP) constitute the major components of MEOS. Cytochrome P450 2E1 (CYP2E1) in MEOS is one of the major ROS generators in liver and is considered to be contributive to ALD. Our labs have been studying the relationship between CYP2E1 and ALD for many years. Recently, we found that human CYP2A6 and its mouse analog CYP2A5 are also induced by alcohol. In mice, the alcohol induction of CYP2A5 is CYP2E1-dependent. Unlike CYP2E1, CYP2A5 protects against the development of ALD. The relationship of CYP2E1, CYP2A5, and ALD is a major focus of this review.

Indexed as

Alcohol OxidoreductasesAnimalsCytochrome P-450 Enzyme SystemHumansLiver Diseases, AlcoholicAlcohol OxidoreductasesCytochrome P-450 Enzyme Systemmicrosomal ethanol-oxidizing systemalcoholic liver diseaseAlcohol inductionantioxidantsautophagycoumarin 7-hydroxylaseCYP2A5CYP2A6CYP2E1FGF21HIF-1αinteractionsliver fibrosisLPSMAPKnicotineNrf2PPARαpyrazolereactive oxygen species.TNFα

Identifiers

PMID29637855
PMCPMC6053342
OpenAlexW2797252933

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.