Role of cellular, molecular and tumor microenvironment in hepatocellular carcinoma: Possible targets and future directions in the regorafenib era.
Sarun JuengpanicWin TopatanaChen LuDaniel StaiculescuShijie LiJiasheng CaoJiacheng LinJiahao HuMingyu ChenJiang ChenXiujun CaiPublished in: International journal of cancer (2020)
Hepatocellular carcinoma (HCC) remains as one of the major causes of cancer-related mortality, despite the recent development of new therapeutic options. Regorafenib, an oral multikinase inhibitor, is the first systemic therapy that has a survival benefit for patients with advanced HCC that have a poor response to sorafenib. Even though regorafenib has been approved by the FDA, the clinical trial for regorafenib treatment does not show significant improvement in overall survival. The impaired efficacy of regorafenib caused by various resistance mechanisms, including epithelial-mesenchymal transitions, inflammation, angiogenesis, hypoxia, oxidative stress, fibrosis and autophagy, still needs to be resolved. In this review, we provide insight on regorafenib microenvironmental, molecular and cellular mechanisms and interactions in HCC treatment. The aim of this review is to help physicians select patients that would obtain the maximal benefits from regorafenib in HCC therapy.
Keyphrases
- metastatic colorectal cancer
- oxidative stress
- clinical trial
- endothelial cells
- stem cells
- primary care
- signaling pathway
- dna damage
- bone marrow
- cardiovascular disease
- coronary artery disease
- cardiovascular events
- risk factors
- single molecule
- endoplasmic reticulum stress
- mesenchymal stem cells
- combination therapy
- blood pressure
- induced apoptosis
- heart rate
- resistance training
- patient reported outcomes
- patient reported
- wound healing