| Literature DB >> 26077472 |
Eric A Lee1, Leonard Angka1, Sarah-Grace Rota1, Thomas Hanlon1, Andrew Mitchell2, Rose Hurren3, Xiao Ming Wang3, Marcela Gronda3, Ezel Boyaci4, Barbara Bojko4, Mark Minden3, Shrivani Sriskanthadevan3, Alessandro Datti5, Jeffery L Wrana6, Andrea Edginton1, Janusz Pawliszyn4, Jamie W Joseph1, Joe Quadrilatero2, Aaron D Schimmer3, Paul A Spagnuolo7.
Abstract
Treatment regimens for acute myeloid leukemia (AML) continue to offer weak clinical outcomes. Through a high-throughput cell-based screen, we identified avocatin B, a lipid derived from avocado fruit, as a novel compound with cytotoxic activity in AML. Avocatin B reduced human primary AML cell viability without effect on normal peripheral blood stem cells. Functional stem cell assays demonstrated selectivity toward AML progenitor and stem cells without effects on normal hematopoietic stem cells. Mechanistic investigations indicated that cytotoxicity relied on mitochondrial localization, as cells lacking functional mitochondria or CPT1, the enzyme that facilitates mitochondria lipid transport, were insensitive to avocatin B. Furthermore, avocatin B inhibited fatty acid oxidation and decreased NADPH levels, resulting in ROS-dependent leukemia cell death characterized by the release of mitochondrial proteins, apoptosis-inducing factor, and cytochrome c. This study reveals a novel strategy for selective leukemia cell eradication based on a specific difference in mitochondrial function. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26077472 DOI: 10.1158/0008-5472.CAN-14-2676
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701