Cited by 148Pharmacogenetics and Drug MetabolismAlcohol Consumption and Health EffectsDrug-Induced Hepatotoxicity and Protection

Ethanol‐Inducible Cytochrome P450 (CYP2E1): Biochemistry, Molecular Biology and Clinical Relevance: 1996 Update

Song, B.J., Cederbaum, Arthur I.·1996·Alcoholism: Clinical and Experimental Research

Integrity signals

Registry

Crossref · 10.1111/j.1530-0277.1996.tb01764.x

Cites

116 of 116 references verified0 citation errors · 0 not checkable

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  • Formation of adduct proteins can prolong protein half-lives and accumulate as aggregated proteins; AA adduct formation and ubiquitin conjugation may compete for common lysine residues, so when lysine residues are occupied by reactive acetaldehyde, lipid aldehydes, AGEs, or AA, adducts persist and may aggregate due to lack of free lysine for ubiquitin conjugation and proteolysis.

    “The formation of adduct proteins can prolong protein half-lives and accumulate as aggregated proteins.”

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Authors
Song, B. J., & Cederbaum, A. I.
Affiliations
  • National Institute on Alcohol Abuse and Alcoholism (US)
  • Mount Sinai Hospital (US)
Venue
Alcoholism: Clinical and Experimental Research
Publisher
Wiley
Published
1996-11
Volume
20
Issue
s8
Pages
138A-146A
ISSN
  • 0145-6008 (ISSN-L)
  • 1530-0277
OpenAlex
W2072244763
Cited by
148
References
116
Citations by year
2024: 1 · 2023: 5 · 2022: 2 · 2021: 5 · 2020: 1 · 2019: 2 · 2018: 3 · 2017: 5 · 2016: 1 · 2015: 5 · 2014: 4 · 2013: 7 · 2012: 7
FWCI
7.76
Type
journal article
Language
en
Open access
closed
Locations
  • Alcoholism Clinical and Experimental Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Alcohol Consumption and Health Effects
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Drug-Induced Hepatotoxicity and Protection
Keywords
CYP2E1, ethanol induction, alcohol metabolism, alcoholic liver disease, oxidative stress, gene expression regulation
MeSH terms
Ethanol, Alcoholism, Animals, Enzyme Induction, Humans, Liver Diseases, Alcoholic, Microsomes, Liver, Polymorphism, Genetic, Gene Expression Regulation, Enzymologic, Reactive Oxygen Species, Cytochrome P-450 CYP2E1

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