Targeting mTOR for the treatment of AML. New agents and new directions.

被引:85
作者
Altman, Jessica K. [1 ]
Sassano, Antonella
Platanias, Leonidas C.
机构
[1] Northwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
关键词
Acute myeloid leukemia; mTOR; TORC2; TORC1; rapamycin; kinase; signaling; chemotherapy; cell survival; ACUTE MYELOID-LEUKEMIA; ACUTE MYELOGENOUS LEUKEMIA; PHOSPHOINOSITIDE 3-KINASE PATHWAY; RENAL-CELL CARCINOMA; INITIATION-FACTOR; 4A; MAMMALIAN TARGET; SUPPRESSOR PDCD4; EUKARYOTIC TRANSLATION; MOTIF PHOSPHORYLATION; P110-DELTA ISOFORM;
D O I
10.18632/oncotarget.290
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Despite recent advances in the field, the treatment of patients with acute myeloid leukemia (AML) remains challenging and difficult. Although chemotherapeutic agents induce remissions in a large number of patients, many of them eventually relapse and die. A major goal for the development of new approaches for the treatment of AML is to enhance the antileukemic effects of standard chemotherapeutics and to design effective combinations targeting non-overlapping cellular pathways. The PI3K/Akt/mTOR signaling pathway plays a critical role in survival and growth of malignant cells and its targeting has been the focus of extensive work and research efforts over the last two decades. It now appears possible that a major limitation of the first generation of mTOR inhibitors can be overcome by a new class of catalytic inhibitors of mTOR. There is emerging evidence that such compounds target both TORC1 and TORC2 and elicit much more potent responses against early leukemic precursors in vitro. In addition, recent studies have shown that combinations of such agents with cytarabine result in enhanced antileukemic responses in vitro, raising the prospect and potential of use of these agents in combination regimens for the treatment of AML.
引用
收藏
页码:510 / 517
页数:8
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