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Alpha-foetoprotein (AFP): A multi-purpose marker in hepatocellular carcinoma
Chloé Sauzay1, Alexandra Petit2, Anne-Marie Bourgeois2
1Service de Biochimie, Centre de Biologie Humaine (CBH), CHU Amiens Sud, France; EA4666, Université de Picardie Jules Verne (UPJV), Amiens, France.
Alpha-foetoprotein (AFP) is a key tumor marker for liver cancer (HCC). Recent research highlights its role in guiding treatment decisions, monitoring therapy, and understanding tumor progression through proteostasis and the Unfolded Protein Response (UPR).
Area of Science:
- Oncology
- Biochemistry
- Hepatology
Background:
- Alpha-foetoprotein (AFP) is a well-established protein tumor marker.
- Its utility in screening and diagnosing hepatocellular carcinoma (HCC) remains under discussion.
- Emerging research explores AFP's role beyond diagnosis, including therapeutic guidance and monitoring.
Purpose of the Study:
- To summarize recent studies on AFP quantification in HCC management.
- To highlight AFP's role in determining liver transplantation suitability and monitoring sorafenib treatment.
- To discuss novel insights into AFP regulation by tumor proteostasis and the Unfolded Protein Response (UPR).
Main Methods:
- Literature review of recent studies on AFP in HCC.
- Analysis of AFP's role in therapeutic decision-making and treatment monitoring.
- Exploration of new regulatory mechanisms of AFP, including proteostasis and UPR.
Main Results:
- AFP quantification is valuable for guiding liver transplantation and monitoring targeted therapies like sorafenib.
- Recent studies reveal AFP's active involvement in tumor progression.
- New regulatory pathways for AFP, involving tumor proteostasis and UPR, have been identified.
Conclusions:
- Updated understanding of AFP's role in HCC management, from diagnosis to treatment monitoring.
- Implications of novel AFP regulation mechanisms for interpreting serum levels and therapeutic strategies.
- New perspectives for studying tumor proteostasis using AFP as a marker.
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