Molecular Mechanisms of Alcohol-Associated Liver Disease

Description

This session explores the molecular and cellular mechanisms driving alcohol-associated liver disease. Presentations examine impaired lipophagy and lysosomal damage in hepatocellular steatosis, epigenetic remodeling of immune and inflammatory pathways, and novel approaches to targeting TNF-α signaling without systemic cytokine blockade. Additional talks reveal a circRNA axis governing sphingolipid dysregulation, an alcohol-induced bile acid intermediate modulating intestinal FXR-FGF15/19 signaling, and UBC9-driven transcriptional reprogramming in macrophage inflammatory activation. Together, these studies illuminate emerging pathways and potential therapeutic targets across lipid metabolism, epigenetics, inflammation, and the gut-liver axis.

Presentations

8:00 AM - 8:15 AM
Convention Center - Bluebird Ballroom 1C
Recorded session

Ethanol induced hepatocellular steatosis is a catabolic lipophagy defect resulting from lysosome damage. 

Sandhya Sen, PhD | Abstract Presenter
8:15 AM - 8:30 AM
Convention Center - Bluebird Ballroom 1C
Recorded session

Multi-Compartment DNA Methylation Analysis Reveals Immune and Inflammatory Epigenetic Remodeling in Alcohol-Associated Hepatitis

Brandon J Peiffer, Ph.D. | Abstract Presenter
8:30 AM - 8:45 AM
Convention Center - Bluebird Ballroom 1C
Recorded session

Targeting Pathologic TNF-α Signaling in ALD Without Systemic Cytokine Blockade

Armen Petrosyan, PhD | Abstract Presenter
8:45 AM - 9:00 AM
Convention Center - Bluebird Ballroom 1C
Recorded session

A Novel circRNA Regulatory Axis Driving Sphingolipid Dysregulation in Alcohol-Associated Liver Disease

Hongkun Lu | Abstract Presenter
9:00 AM - 9:15 AM
Convention Center - Bluebird Ballroom 1C
Recorded session

An alcohol-induced bile acid intermediate regulates intestinal FXR-FGF15/19 signaling

Weiran Wang, PhD | Abstract Presenter
9:15 AM - 9:30 AM
Convention Center - Bluebird Ballroom 1C
Recorded session

UBC9 phosphorylation reprograms SRC expression through JunB/AP-1 feedback axis during macrophage inflammatory activation in alcohol-associated liver disease 

Manisha Dagar, PhD | Abstract Presenter

Objectives

  • Explain how lysosomal damage and defective lipophagy contribute to ethanol-induced hepatocellular steatosis
  • Describe epigenetic and transcriptional mechanisms, including DNA methylation remodeling and UBC9/JunB/AP-1 signaling, that regulate immune and inflammatory responses in alcohol-associated liver disease
  • Evaluate emerging molecular pathways, including circRNA-driven sphingolipid dysregulation and alcohol-induced bile acid modulation of intestinal FXR-FGF15/19 signaling, in ALD pathogenesis
  • Assess novel therapeutic strategies, such as targeted TNF- inhibition, for their potential to modify disease progression in alcohol-associated liver disease