Role of epidermal growth factor receptor in liver injury and lipid metabolism: Emerging new roles for an old receptor
Abstract
Epidermal growth factor receptor (EGFR) is conventionally known to play a crucial role in hepatocyte proliferation, liver regeneration and is also associated with hepatocellular carcinogenesis. In addition to these proliferative roles, EGFR has also implicated in apoptotic cell death signaling in various hepatic cells, mitochondrial dysfunction and acute liver necrosis in a clinically relevant murine model of acetaminophen overdose, warranting further comprehensive exploration of this paradoxical role of EGFR in hepatotoxicity. Apart from ligand dependent activation, EGFR can also be activated in ligand-independent manner, which is mainly associated to liver injury. Recent evidence has also emerged demonstrating important role of EGFR in lipid and fatty acid metabolism in quiescent and regenerating liver. Based on these findings, EGFR has also been shown to play an important role in steatosis in clinically relevant murine NAFLD models via regulating master transcription factors governing fatty acid synthesis and lipolysis. Moreover, several lines of evidences indicate that EGFR is also involved in hepatocellular injury, oxidative stress, inflammation, direct stellate cell activation and fibrosis in chronic liver injury models, including repeated CCl 4 exposure, high-fat diet and fast-food diet models. In addition to briefly summarizing role of EGFR in liver regeneration, this review comprehensively discusses all these non-conventional emerging roles of EGFR. Considering evide…
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Epidermal growth factor and transforming growth factor-alpha play key roles in hepatocyte proliferation and survival by activating the cell cycle and protecting hepatocytes from a stressful environment.
“Epidermal growth factor and transforming growth factor-alpha play key roles in hepatocyte proliferation and survival. These growth factors activate the cell cycle and protect hepatocytes from a stressful environment, ensuring the continuation of the regenerative process[62].”
From Liver regeneration after partial hepatectomy: Triggers and mechanisms (2025) · cites this paper as [62]
Cites
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Bhushan, B., Stoops, J. W., Mars, W. M., Orr, A., Bowen, W. C., Paranjpe, S., & Michalopoulos, G. K. (2019) · Hepatology · doi:10.1002/hep.30109 · Cited by 49 · see citing works
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Molecular mechanisms in liver repair and regeneration: from physiology to therapeutics
Ma, X., Huang, T., Chen, X., Li, Q., Liao, M., Fu, L., Huang, J., Yuan, K., Wang, Z., & Zeng, Y. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02104-8 · Cited by 133 · see citing works
Liver regeneration after partial hepatectomy: Triggers and mechanisms
Korchilava, B., Khachidze, T., Megrelishvili, N., Svanadze, L., Kakabadze, M., Tsomaia, K., Jintcharadze, M., & Kordzaia, D. (2025) · World Journal of Hepatology · doi:10.4254/wjh.v17.i7.107378 · Cited by 21 · see citing works
- Authors
- Bhushan, B., & Michalopoulos, G. K.
- Affiliations
- University of Pittsburgh (US)
- Corresponding author
- Michalopoulos, George K.
- Venue
- Chemico-Biological Interactions
- Publisher
- Elsevier BV
- Published
- 2020-06
- Volume
- 324
- Pages
- 109090
- ISSN
- 0009-2797 (ISSN-L)
- OpenAlex
- W3015357373
- Cited by
- 66
- References
- 4
- Citations by year
- 2026: 9 · 2025: 10 · 2024: 14 · 2023: 8 · 2022: 17 · 2021: 6 · 2020: 2
- FWCI
- 1.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Chemico-Biological Interactions (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Cleveland Foundation
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Drug-Induced Hepatotoxicity and Protection
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Keywords
- epidermal growth factor receptor, liver injury, hepatotoxicity, lipid metabolism, fatty acid synthesis, lipolysis, non-alcoholic fatty liver disease, steatosis, liver regeneration, hepatocyte injury, liver fibrosis, stellate cell activation, oxidative stress, liver inflammation, ligand-independent receptor activation, alcoholic liver disease, therapeutic target
- MeSH terms
- Animals, Humans, Liver Diseases, Liver Regeneration, Cell Death, Lipid Metabolism, Hepatic Stellate Cells, ErbB Receptors
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