Synergistic effect of inhibiting translation initiation in combination with cytotoxic agents in acute myelogenous leukemia cells

被引：40

作者：

Cencic, Regina ^{[1
]}

Carrier, Marilyn ^{[1
]}

Trnkus, Amanda ^{[1
]}

Porco, John A., Jr. ^{[2
]}

Minden, Mark ^{[3
]}

Pelletier, Jerry ^{[1
,4
]}

机构：

[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada

[2] Boston Univ, Ctr Chem Methodol & Lib Dev, Dept Chem, Boston, MA 02215 USA

[3] Univ Toronto, Princess Margaret Hosp, Dept Med Oncol & Hematol, Toronto, ON, Canada

[4] McGill Univ, Goodman Canc Ctr, Montreal, PQ H3G 1Y6, Canada

来源：

LEUKEMIA RESEARCH | 2010年 / 34卷 / 04期

关键词：

Silvestrol; AML; Translation initiation; Synergy; Chemotherapy; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; BH3 MIMETIC ABT-737; DOWN-REGULATION; THERAPEUTIC SUPPRESSION; MESSENGER-RNAS; IN-VITRO; APOPTOSIS; MCL-1; ACTIVATION;

D O I：

10.1016/j.leukres.2009.07.043

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

We have previously shown that inhibition of translation initiation, using the small molecule inhibitor silvestrol, induces apoptosis in a pre-clinical murine lymphoma model when combined with daunorubicin. Silvestrol blocks ribosome recruitment by targeting the RNA helicase, eIF4A, which is required for this process. Here we investigate the sensitivity of acute myelogenous leukemia (AML) cell lines to protein synthesis inhibition in combination with the standard cytotoxic agents daunorubicin, etoposide, and cytarabine. Silvestrol shows synergy with standard-of-care agents in AML cell lines and synergizes with ABT-737, a small molecule inhibitor of Bcl-XL and Bcl-2. The in vitro synergy between silvestrol and the cytotoxic drugs used in AML therapy provides a basis for in vivo evaluation of these combinations. (C) 2009 Elsevier Ltd. All rights reserved.

引用

页码：535 / 541

页数：7

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