| Literature DB >> 34714696 |
Cornelis J F van Noorden1,2, Barbara Breznik1, Metka Novak1, Amber J van Dijck2, Saloua Tanan2, Miloš Vittori3, Urban Bogataj3, Noëlle Bakker2, Joseph D Khoury4, Remco J Molenaar1,5, Vashendriya V V Hira1.
Abstract
Energy production by means of ATP synthesis in cancer cells has been investigated frequently as a potential therapeutic target in this century. Both (an)aerobic glycolysis and oxidative phosphorylation (OXPHOS) have been studied. Here, we review recent literature on energy production in glioblastoma stem cells (GSCs) and leukemic stem cells (LSCs) versus their normal counterparts, neural stem cells (NSCs) and hematopoietic stem cells (HSCs), respectively. These two cancer stem cell types were compared because their niches in glioblastoma tumors and in bone marrow are similar. In this study, it became apparent that (1) ATP is produced in NSCs and HSCs by anaerobic glycolysis, whereas fatty acid oxidation (FAO) is essential for their stem cell fate and (2) ATP is produced in GSCs and LSCs by OXPHOS despite the hypoxic conditions in their niches with FAO and amino acids providing its substrate. These metabolic processes appeared to be under tight control of cellular regulation mechanisms which are discussed in depth. However, our conclusion is that systemic therapeutic targeting of ATP production via glycolysis or OXPHOS is not an attractive option because of its unwanted side effects in cancer patients.Entities:
Keywords: angiogenesis; bone marrow; brain tumors; cancer stem cells; hematopoietic stem cells; leukemia; leukemic stem cells; metabolism; neural stem cells; niches; stem cells; stemness; tumor heterogeneity; tumor immune infiltrate; tumor microenvironment
Mesh：
Year: 2021 PMID： 34714696 PMCID： PMC8721571 DOI： 10.1369/00221554211054585
Source DB: PubMed Journal: J Histochem Cytochem ISSN： 0022-1554 Impact factor: 2.479