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Role of cellular, molecular and tumor microenvironment in hepatocellular carcinoma: Possible targets and future directions in the regorafenib era
- Source :
- International journal of cancerReferences. 147(7)
- Publication Year :
- 2019
-
Abstract
- 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.
- Subjects :
- Sorafenib
Oncology
Cancer Research
medicine.medical_specialty
Carcinoma, Hepatocellular
Epithelial-Mesenchymal Transition
Angiogenesis
Pyridines
Antineoplastic Agents
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Fibrosis
Internal medicine
Regorafenib
medicine
Tumor Microenvironment
Humans
Gene Regulatory Networks
Tumor microenvironment
Clinical Trials as Topic
business.industry
Phenylurea Compounds
Autophagy
Liver Neoplasms
medicine.disease
digestive system diseases
Clinical trial
chemistry
Drug Resistance, Neoplasm
030220 oncology & carcinogenesis
Hepatocellular carcinoma
Tumor Hypoxia
business
medicine.drug
Subjects
Details
- ISSN :
- 10970215
- Volume :
- 147
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- International journal of cancerReferences
- Accession number :
- edsair.doi.dedup.....44957d5dc48fc8c977e261e53cb5ecc5