髓系白血病
白血病
线粒体
背景(考古学)
癌症研究
氧化磷酸化
干细胞
生物
髓样
医学
免疫学
细胞生物学
生物化学
古生物学
作者
Ryan J. Stubbins,Irina A. Maksakova,David Sanford,A. MAUREEN ROUHI,Florian Kuchenbauer
标识
DOI:10.1080/10428194.2021.1910685
摘要
There has been an explosion of knowledge about the role of metabolism and the mitochondria in acute myeloid leukemia (AML). We have also recently seen several waves of novel therapies change the treatment landscape for AML, such as the selective B-cell lymphoma 2 (BCL-2) inhibitor venetoclax. In this new context, we review the rapidly advancing literature on the role of metabolism and the mitochondria in AML pathogenesis, and how these are interwoven with the mechanisms of action for novel therapeutics in AML. We also review the role of oxidative phosphorylation (OxPhos) in maintaining leukemia stem cells (LSCs), how recurrent genomic alterations in AML alter downstream metabolism, and focus on how the BCL-2 pathway and the mitochondria are inextricably linked in AML. Thus, we provide an overview of the mitochondria and metabolism in the context of our new therapeutic world for AML and outline how targeting these vulnerabilities may produce novel therapeutic strategies.
科研通智能强力驱动
Strongly Powered by AbleSci AI