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Inhibition of mitochondrial complex III induces differentiation in acute myeloid leukemia.
- Source :
-
Biochemical & Biophysical Research Communications . Apr2021, Vol. 547, p162-168. 7p. - Publication Year :
- 2021
-
Abstract
- Although acute myeloid leukemia (AML) is a highly heterogeneous disease with diverse genetic subsets, one hallmark of AML blasts is myeloid differentiation blockade. Extensive evidence has indicated that differentiation induction therapy represents a promising treatment strategy. Here, we identified that the pharmacological inhibition of the mitochondrial electron transport chain (ETC) complex III by antimycin A inhibits proliferation and promotes cellular differentiation of AML cells. Mechanistically, we showed that the inhibition of dihydroorotate dehydrogenase (DHODH), a rate-limiting enzyme in de novo pyrimidine biosynthesis, is involved in antimycin A-induced differentiation. The activity of antimycin A could be reversed by supplement of excessive amounts of exogenous uridine as well as orotic acid, the product of DHODH. Furthermore, we also found that complex III inhibition exerts a synergistic effect in differentiation induction combined with DHODH inhibitor brequinar as well as with the pyrimidine salvage pathway inhibitor dipyridamole. Collectively, our study uncovered the link between mitochondrial complex III and AML differentiation and may provide further insight into the potential application of mitochondrial complex III inhibitor as a mono or combination treatment in differentiation therapy of AML. • Our study uncovered the inhibition of mitochondrial complex III-induced AML cell differentiation as well as the underlying mechanisms. • The concomitant blockade of the complex III and pyrimidine biosynthesis pathways, including the de novo and salvage pathway, exerts a synergistic effect in inducing AML cell differentiation. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 0006291X
- Volume :
- 547
- Database :
- Academic Search Index
- Journal :
- Biochemical & Biophysical Research Communications
- Publication Type :
- Academic Journal
- Accession number :
- 148982972
- Full Text :
- https://doi.org/10.1016/j.bbrc.2021.02.027