ABT-199, a BH3 mimetic that specifically targets Bcl-2, enhances the antitumor activity of chemotherapy, bortezomib and JQ1 in "double hit" lymphoma cells

被引:52
|
作者
Johnson-Farley, Nadine
Veliz, Jonny
Bhagavathi, S.
Bertino, Joseph R.
机构
[1] Rutgers Canc Inst New Jersey, New Brunswick, NJ 08903 USA
[2] Robert Wood Johnson Sch Med, New Brunswick, NJ USA
基金
美国国家卫生研究院;
关键词
Cell lines and animal models; chemotherapeutic approaches; lymphoma and Hodgkin disease; BET BROMODOMAIN INHIBITION; MCL-1; DOWN-REGULATION; GLIOMA-CELLS; PHASE-I; MYC; SURVIVIN; NAVITOCLAX; EFFICACY; POTENT;
D O I
10.3109/10428194.2014.981172
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Double hit lymphoma (DHL) is a recently recognized lymphoma with a survival of less than 2 years. Both ABT-737, a Bcl-2/Bcl-XL inhibitor, and ABT-199, which selectively targets Bcl-2, were potently cytotoxic against DHL cell lines Sc-1 and Ocl-LY18, the RL cell line and primary human DHL cells, but not Ramos cells, which lack Bcl-2 expression. ABT-199 was more potent than ABT-737, and is the most promising of the BH3 mimetics to date. The DHL cell lines were also sensitive (<200 nM) to doxorubicin, methotrexate, cytarabine and the proteosome inhibitor, bortezomib. The combination of chemotherapy with ABT-199 and doxorubicin or cytarabine, bortezomib, YM-155 and JQ1 produced synergistic cell kill against the DHL cell lines. Cells from a patient with DHL were also sensitive to JQ1 and bortezomib, providing a rationale for a clinical trial of these combinations in patients with relapsed DHL.
引用
收藏
页码:2146 / 2152
页数:7
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