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Sphingolipid metabolism determines the therapeutic efficacy of nanoliposomal ceramide in acute myeloid leukemia.
Academic Article
Author's Version
View record in Web of Science ®
Overview
Research
Identity
Additional Document Info
Overview
Abstract
Distinct sphingolipid metabolism of AML with MDS-related changes defines unique sensitivity to nanoliposomal C6-ceramide. Vinblastine alters sphingolipid metabolism to enhance the sensitivity of AML to nanoliposomal C6-ceramide.
Authors
Barth, Brian M
Wang, Weiyuan
Toran, Paul T
Fox, Todd E
Annageldiyev, Charyguly
Ondrasik, Regina M
Keasey, Nicole R
Brown, Timothy J
Devine, Viola G
Sullivan, Emily C
Cote, Andrea L
Papakotsi, Vasiliki
Tan, Su-Fern
Shanmugavelandy, Sriram S
Deering, Tye G
Needle, David
Stern, Stephan T
Zhu, Junjia
Liao, Jason
Viny, Aaron D
Feith, David J
Levine, Ross L
Wang, Hong-Gang
Loughran, Thomas P
Sharma, Arati
Kester, Mark
Claxton, David F
Status
published
Publication Date
September 10, 2019
Has Subject Area
Antineoplastic Agents, Phytogenic
Ceramides
Drug Carriers
Drug Delivery Systems
Humans
Leukemia, Myeloid, Acute
Liposomes
Nanostructures
Sphingolipids
Treatment Outcome
Vinblastine
Published In
Blood Adv
Journal
Research
Keywords
Antineoplastic Agents, Phytogenic
Ceramides
Drug Carriers
Drug Delivery Systems
Humans
Leukemia, Myeloid, Acute
Liposomes
Nanostructures
Sphingolipids
Treatment Outcome
Vinblastine
Identity
Digital Object Identifier (doi)
https://doi.org/10.1182/bloodadvances.2018021295
Additional Document Info
Start Page
2598
End Page
2603
Volume
3
Issue
17