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An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
Gene therapy strategies for hepatocellular carcinoma
1Hepatitis Research Center, National Taiwan University Hospital and Graduate Institute of Microbiology, National Taiwan University College of Medicine, 7 Chung-Shan S. Road, Taipei 10016, Taiwan, R.O.C. lihhwa@ha.mc.ntu.edu.tw
Abstract:
Hepatocellular carcinoma (HCC) is one of the most frequent cancers worldwide. Effective therapy to this cancer is currently lacking, creating an urgent need for new therapeutic strategies for HCC. Gene therapy approach that relies on the transduction of cells with genetic materials, such as apoptotic genes, suicide genes, genes coding for antiangiogenic factors or immunomodulatory molecules, small interfering RNA (siRNA), or oncolytic viral vectors, may provide a promising strategy. The aforementioned strategies have been largely evaluated in the animal models with HCC or liver metastasis. Due to the diversity of vectors and therapeutic genes, being used alone or in combination, gene therapy approach may generate great beneficial effects to control the growth of tumors within the liver.
Insights
Gene therapy offers a promising strategy for treating hepatocellular carcinoma (HCC), a common cancer lacking effective treatments. This approach uses genetic materials to combat liver tumors, showing potential in preclinical models.
Area of Science:
- Hepatocellular carcinoma (HCC) research
- Gene therapy applications
- Oncology therapeutics
Background:
- Hepatocellular carcinoma (HCC) is a globally prevalent cancer with limited effective treatment options.
- There is a significant unmet need for novel therapeutic strategies to manage HCC.
- Gene therapy presents a potential avenue for developing new treatments for liver cancer.
Purpose of the Study:
- To explore the potential of gene therapy as a therapeutic strategy for hepatocellular carcinoma (HCC).
- To review various gene therapy approaches being investigated for HCC treatment.
- To highlight the promise of gene therapy in controlling liver tumor growth.
Main Methods:
- Review of gene therapy strategies including apoptotic genes, suicide genes, antiangiogenic factors, immunomodulatory molecules, small interfering RNA (siRNA), and oncolytic viral vectors.
- Evaluation of these strategies in animal models of HCC and liver metastasis.
- Assessment of the combination of different vectors and therapeutic genes.
Main Results:
- Gene therapy approaches have shown promise in preclinical studies for HCC.
- Diverse gene therapy vectors and genes, used individually or in combination, are being investigated.
- These strategies have demonstrated potential in controlling tumor growth in liver cancer models.
Conclusions:
- Gene therapy represents a promising strategy for the development of novel treatments for hepatocellular carcinoma (HCC).
- The use of various genetic materials and delivery vectors offers a versatile approach to combat liver cancer.
- Further research and clinical translation of gene therapy hold potential for improving HCC patient outcomes.
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