| Literature DB >> 31176254 |
Ching-Wen Chang1, Jeng-Fan Lo2, Xin Wei Wang3.
Abstract
Primary liver cancer (PLC) is heterogeneous and it is an aggressive malignancy with a poor prognostic outcome. Current evidence suggests that PLC tumorigenesis is driven by rare subpopulations of cancer stem cells (CSCs), which contribute to tumor initiation, progression, and therapy resistance through particular molecular mechanisms. Energy metabolism and mitochondrial function play an important role in the regulation of cancer stemness and stem cell specifications. Since the role of mitochondrial function as central hubs in cell growth and survival, studies on the critical physiological mechanisms of the liver underlying their therapy-resistant phenotype is important. In this review, we focus on liver CSC-related mitochondrial metabolism that contributes to the liver CSC features, in terms of enhanced drug-resistance and increased tumorigenicity, and to discuss their roles on potential therapies windows for PLC therapies. Published by Elsevier B.V.Entities:
Mesh:
Year: 2019 PMID: 31176254 PMCID: PMC6612304 DOI: 10.1016/j.diff.2019.04.001
Source DB: PubMed Journal: Differentiation ISSN: 0301-4681 Impact factor: 3.880