Current Status of Gene Therapy in Hepatocellular Carcinoma.
Saranya Chidambaranathan ReghupatyDevanand SarkarPublished in: Cancers (2019)
Hepatocellular carcinoma (HCC) is the fifth most common cancer and the second leading cause of cancer related deaths world-wide. Liver transplantation, surgical resection, trans-arterial chemoembolization, and radio frequency ablation are effective strategies to treat early stage HCC. Unfortunately, HCC is usually diagnosed at an advanced stage and there are not many treatment options for late stage HCC. First-line therapy for late stage HCC includes sorafenib and lenvatinib. However, these treatments provide only an approximate three month increase in survival. Besides, they cannot specifically target cancer cells that lead to a wide array of side effects. Patients on these drugs develop resistance within a few months and have to rely on second-line therapy that includes regorafenib, pembrolizumab, nivolumab, and cabometyx. These disadvantages make gene therapy approach to treat HCC an attractive option. The two important questions that researchers have been trying to answer in the last 2-3 decades are what genes should be targeted and what delivery systems should be used. The objective of this review is to analyze the changing landscape of HCC gene therapy, with a focus on these two questions.
Keyphrases
- gene therapy
- early stage
- end stage renal disease
- current status
- chronic kidney disease
- newly diagnosed
- stem cells
- mass spectrometry
- high throughput
- gene expression
- prognostic factors
- single cell
- cancer therapy
- radiation therapy
- dna methylation
- young adults
- neoadjuvant chemotherapy
- patient reported
- smoking cessation
- genome wide identification
- childhood cancer