In vivo efficacy of a novel histone deacetylase inhibitor in combination with radiatio or the treatment of gliomas

被引:44
作者
Entin-Meer, Michal [1 ]
Yang, Xiaodong
VandenBerg, Scott R.
Lamborn, Kathleen R.
Nudelman, Abraham
Rephaeli, Ada
Haas-Kogan, Daphne Adele
机构
[1] Univ Calif San Francisco, Dept Radiat Oncol Neurol Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Pathol & Neurol Surg, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Brain Tumor Res Ctr, San Francisco, CA 94143 USA
[6] Bar Ilan Univ, Dept Chem, Ramat Gan, Israel
[7] Tel Aviv Univ, Sackler Sch Med, Felsenstein Med Res Ctr, IL-49100 Petah Tiqwa, Israel
关键词
AN-9; gamma-H2AX phosphorylation; glioma; histone deacetylase inhibitor; radiation; temozolomide;
D O I
10.1215/15228517-2006-032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Histone modification has emerged as a promising approach to cancer therapy. We explored the in vivo efficacy of a butyric acid derivative, pivaloyloxymethyl butyrate (AN-9), for the treatment of gliomas. Relative to control and single-modality treatments, the combination of AN-9 and radiation significantly inhibited tumor growth and prolonged time to failure in mice bearing glioma xenografts. The enhanced response to radiation was accompanied by inhibition of cellular proliferation and by increased phosphorylation of H2AX, implicating DNA double-strand breaks in the antineoplastic effects of AN-9 and radiation. The data suggest that AN-9 in combination with radiation may be an effective therapy for malignant gliomas.
引用
收藏
页码:82 / 88
页数:7
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