Valproic Acid Enhances the Anti-tumor Effect of Pegylated Interferon-α Towards Pancreatic Cancer Cell Lines

被引：0
|
作者：
Sugimoto, Koji [1 ]
Shimada, Mitsuo [1 ]
Utsunomiya, Toru [1 ]
Morine, Yuji [1 ]
Imura, Satoru [1 ]
Ikemoto, Tetsuya [1 ]
Iwahashi, Shuichi [1 ]
机构：
[1] Univ Tokushima, Dept Surg, Inst Hlth Biosci, Tokushima 7708503, Japan
来源：
ANTICANCER RESEARCH | 2014年 / 34卷 / 07期
关键词：
Histone deacetylase inhibitor; valproic acid; pegylated interferon-alpha; pancreatic cancer; HISTONE DEACETYLASE INHIBITORS; REGULATORY FACTOR-8; IN-VITRO; COMBINATION THERAPY; IFN-ALPHA; EXPRESSION; APOPTOSIS; ANGIOGENESIS; REGRESSION; CARCINOMA;
D O I：
暂无
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
Background: Valproic acid (VPA) acts as a specific inhibitor of class I HDACs and it use has been proven to be safe since a long time. Materials and Methods: In the present study, we investigated the effect of VPA in the combination with pegylated interferon-alpha (PEG-IFN alpha) in inhibition of cell proliferation of human pancreatic cancer cell lines. Results: VPA enhanced the effect of PEG-IFNa, and the effect was decreased by the caspase inhibitor. VPA alone and VPA in combination with PEG-IFNa increased the expression of interferon-alpha receptor and interferon regulatory factor 8. Conclusion: The combination of VPA and PEG-IFN alpha can be useful for the treatment of pancreatic cancer.
引用
收藏
页码：3403 / 3409
页数：7
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