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Updated: Feb 11, 2026

Human Liver Microphysiological System for Assessing Drug-Induced Liver Toxicity In Vitro
Published on: January 31, 2022
LncRNA-Regulated Autophagy and its Potential Role in Drug-Induced Liver Injury
Juan Zhou1, Yi Li2, XinYu Liu1
1Liver Diseases Center, Department of Infectious Diseases, The Second Xiangya Hospital, Central South University, Changsha, Hunan, P.R. China.
Long noncoding RNAs (lncRNAs) regulate autophagy, a cellular process vital for clearing damaged components. This review explores how lncRNAs impact autophagy in drug-induced liver injury (DILI), offering insights into disease mechanisms.
Area of Science:
- Cellular Biology
- Molecular Biology
- Hepatology
Background:
- Autophagy is a critical cellular process involved in maintaining homeostasis and responding to stress.
- Dysregulation of autophagy is implicated in various pathological conditions, including drug-induced liver injury (DILI).
- Long noncoding RNAs (lncRNAs) are emerging as key regulators of cellular processes, including autophagy.
Purpose of the Study:
- To review recent literature on the role of autophagy in DILI.
- To elucidate the regulatory mechanisms of autophagy by lncRNAs in the context of DILI.
- To provide insights into potential therapeutic targets for DILI.
Main Methods:
- Comprehensive literature search using keywords such as DILI, autophagy, autophagy-related genes (ATGs), and lncRNA.
- Systematic review and analysis of relevant published studies from major scientific databases.
- Synthesis of findings to describe lncRNA-mediated regulation of autophagy in DILI.
Main Results:
- DILI and its progression to acute liver failure are linked to endoplasmic reticulum stress and subsequent autophagy induction.
- Autophagy plays a protective role in hepatocytes during DILI.
- lncRNAs modulate autophagy by regulating the expression of autophagy-related genes (ATGs).
Conclusions:
- lncRNAs are significant regulators of autophagy in DILI.
- Understanding lncRNA-autophagy pathways offers new perspectives on DILI pathogenesis.
- Further research into lncRNA-miRNA-associated pathways could reveal novel therapeutic strategies for DILI.
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