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Updated: Jun 3, 2026

An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
HCC and angiogenesis: possible targets and future directions
Andrew X Zhu1, Dan G Duda, Dushyant V Sahani
1Massachusetts General Hospital Cancer Center, Harvard Medical School, 55 Fruit Street, Boston, MA 02114, USA. azhu@partners.org
Hepatocellular carcinoma (HCC) is a resistant liver cancer. Anti-VEGF therapy with sorafenib offers improved survival for advanced HCC, paving the way for new targeted treatments.
Area of Science:
- Oncology
- Hepatology
- Vascular Biology
Background:
- Hepatocellular carcinoma (HCC) is the most common primary liver cancer.
- HCC is often resistant to systemic therapies and recurs after local treatments.
- Tumor growth depends on angiogenesis, with Vascular Endothelial Growth Factor (VEGF) being critical.
Purpose of the Study:
- To review the role of VEGF in HCC development and treatment.
- To discuss the significance of anti-VEGF therapy in advanced HCC.
- To explore future directions for targeted therapies in HCC.
Main Methods:
- Review of existing literature on HCC, VEGF, and antiangiogenic therapies.
- Analysis of the impact of VEGF on the tumor microenvironment.
- Examination of clinical trial data for sorafenib in advanced HCC.
Main Results:
- Tumor angiogenesis, driven by VEGF, creates an abnormal microenvironment.
- Anti-VEGF therapy with sorafenib is the first systemic treatment to improve survival in advanced HCC.
- Abnormal tumor vasculature and hypoxia select for more aggressive HCC phenotypes.
Conclusions:
- Targeted antiangiogenic agents hold promise for improving survival in HCC.
- Further research into novel targeted therapies is crucial for advancing HCC treatment.
- Understanding the tumor microenvironment is key to developing effective HCC therapies.
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