Valproic acid sensitizes chronic lymphocytic leukemia cells to apoptosis and restores the balance between pro- and antiapoptotic proteins

被引:47
作者
Bokelmann, Imke [1 ]
Mahlknecht, Ulrich [1 ,2 ]
机构
[1] Univ Heidelberg, Med Ctr, Dept Hematol Oncol, Heidelberg, Germany
[2] Univ Saarland, Med Ctr, Dept Hematol Oncol, Jose Carreras Ctr Immunotherapy & Gene Therapy, D-66424 Homburg, Germany
关键词
D O I
10.2119/2007-00084.Bokelmann
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chronic lymphocytic leukemia (CLL) is one of the most common leukemias in adults in the developed world, Despite significant advances in the treatment of cancer, CLL remains incurable. The main feature of the disease is the generation of circulating B-cells with prolonged survival caused by aberrant apoptosis. In this study, we observe that valproic acid (VPA), a well-established histone deacetylase (HDAC) inhibitor, mediates apoptosis in CLL cells ex vivo through caspase activation via both the extrinsic and the intrinsic apoptosis pathways, as indicated by the activation of the caspase proteins 8 and 9, and cleavage of the proapoptotic protein BID. The Bcl-2/Bax ratio was decreased as a consequence of decreased bcl-2 mRNA levels in response to treatment with VPA. With the results presented in this study, we have identified the HDAC inhibitor VPA as restoring the apoptotic pathways in CLL cells and thus their ability to undergo apoptosis.
引用
收藏
页码:20 / 27
页数:8
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