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Mitochondrial carrier homolog 2 is necessary for AML survival.

Authors :
Khan DH
Mullokandov M
Wu Y
Voisin V
Gronda M
Hurren R
Wang X
MacLean N
Jeyaraju DV
Jitkova Y
Xu GW
Laister R
Seneviratne A
Blatman ZM
Ketela T
Bader GD
Marhon SA
De Carvalho DD
Minden MD
Gross A
Schimmer AD
Source :
Blood [Blood] 2020 Jul 02; Vol. 136 (1), pp. 81-92.
Publication Year :
2020

Abstract

Through a clustered regularly insterspaced short palindromic repeats (CRISPR) screen to identify mitochondrial genes necessary for the growth of acute myeloid leukemia (AML) cells, we identified the mitochondrial outer membrane protein mitochondrial carrier homolog 2 (MTCH2). In AML, knockdown of MTCH2 decreased growth, reduced engraftment potential of stem cells, and induced differentiation. Inhibiting MTCH2 in AML cells increased nuclear pyruvate and pyruvate dehydrogenase (PDH), which induced histone acetylation and subsequently promoted the differentiation of AML cells. Thus, we have defined a new mechanism by which mitochondria and metabolism regulate AML stem cells and gene expression.<br /> (© 2020 by The American Society of Hematology.)

Details

Language :
English
ISSN :
1528-0020
Volume :
136
Issue :
1
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
32299104
Full Text :
https://doi.org/10.1182/blood.2019000106