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Updated: Jun 13, 2025

An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
Targeted therapies in hepatocellular carcinoma: past, present, and future
Rushabh Gujarathi1, Joseph W Franses1, Anjana Pillai2
1Section of Hematology and Oncology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Abstract:
Targeted therapies are the mainstay of systemic therapies for patients with advanced, unresectable, or metastatic hepatocellular carcinoma. Several therapeutic targets, such as c-Met, TGF-β, and FGFR, have been evaluated in the past, though results from these clinical studies failed to show clinical benefit. However, these remain important targets for the future with novel targeted agents and strategies. The Wnt/β-catenin signaling pathway, c-Myc oncogene, GPC3, PPT1 are exciting novel targets, among others, currently undergoing evaluation. Through this review, we aim to provide an overview of previously evaluated and potentially novel therapeutic targets and explore their continued relevance in ongoing and future studies for HCC.
Insights
Targeted therapies for advanced hepatocellular carcinoma (HCC) have faced challenges. This review explores past and novel targets like Wnt/β-catenin, offering insights for future HCC treatment strategies.
Area of Science:
- Oncology
- Pharmacology
Background:
- Targeted therapies are crucial for advanced, unresectable, or metastatic hepatocellular carcinoma (HCC).
- Previous targeted agents focusing on c-Met, TGF-β, and FGFR showed limited clinical benefit in HCC.
- Despite past setbacks, these targets remain relevant for future therapeutic development.
Purpose of the Study:
- To review previously evaluated therapeutic targets in HCC.
- To explore novel and emerging targets for HCC treatment.
- To assess the continued relevance of these targets in ongoing and future HCC studies.
Main Methods:
- Literature review of clinical studies on targeted therapies for HCC.
- Analysis of previously evaluated targets (c-Met, TGF-β, FGFR).
- Identification and discussion of novel targets (Wnt/β-catenin, c-Myc, GPC3, PPT1).
Main Results:
- Several targeted therapies for HCC have been investigated.
- Past targets like c-Met, TGF-β, and FGFR did not demonstrate significant clinical benefit.
- Novel targets including the Wnt/β-catenin pathway, c-Myc, GPC3, and PPT1 are under active investigation.
Conclusions:
- While past targeted therapies for HCC yielded limited success, the identified targets remain important.
- Novel targets show promise for future HCC treatment strategies.
- Continued research into these targets is essential for advancing HCC therapy.
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