Combination of the histone deacetylase inhibitor depsipeptide and 5-fluorouracil upregulates major histocompatibility complex class II and p21 genes and activates caspase-3/7 in human colon cancer HCT-116 cells

被引:34
作者
Okada, Kouji [1 ,2 ]
Hakata, Shuko [1 ]
Terashima, Jun [1 ]
Gamou, Toshie [1 ]
Habano, Wataru [1 ]
Ozawa, Shogo [1 ]
机构
[1] Iwate Med Univ, Sch Pharm, Dept Pharmacodynam & Mol Genet, 2-1-1 Nishitokuta, Yahaba, Iwate 0283694, Japan
[2] Iwate Cent Prefectural Hosp, Dept Pharm, Morioka, Iwate 0200066, Japan
关键词
histone deacetylase inhibitor; depsipeptide; 5-fluorouracil; combination; human colon cancer HCT-116; major histocompatibility complex class II genes; caspase-3/7; activation; p21 (CDKN1A); microarray analysis; CHROMOBACTERIUM-VIOLACEUM NO-968; THYMIDYLATE SYNTHASE; COLORECTAL-CARCINOMA; HDAC INHIBITORS; DOWN-REGULATION; GROWTH ARREST; EXPRESSION; APOPTOSIS; FR901228; CYTOTOXICITY;
D O I
10.3892/or.2016.5008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epigenetic anticancer drugs such as histone deacetylase (HDAC) inhibitors have been combined with existing anticancer drugs for synergistic or additive effects. In the present study, we found that a very low concentration of depsipeptide, an HDAC inhibitor, potentiated the antitumor activity of 5-fluorouracil (5-FU) in a human colon cancer cell model using HCT-116, HT29, and SW48 cells via the inhibition of colony formation ability or cellular viability. Exposure to a combination of 5-FU (1.75 mu M) and 1 nM depsipeptide for 24 and 48 h resulted in a 3- to 4-fold increase in activated caspase-3/7, while 5-FU alone failed to activate caspase-3/7. Microarray and subsequent gene ontology analyses revealed that compared to 5-FU or depsipeptide alone, the combination treatment of 5-FU and depsipeptide upregulated genes related to cell death and the apoptotic process consistent with the inhibition of colony formation and caspase-3/7 activation. These analyses indicated marked upregulation of antigen processing and presentation of peptide or polysaccharide antigen via major histocompatibility complex (MHC) class (GO:0002504) and MHC protein complex (GO:0042611). Compared with vehicle controls, the cells treated with the combination of 5-FU and depsipeptide showed marked induction (3- to 8.5-fold) of expression of MHC class II genes, but not of MHC class I genes. Furthermore, our global analysis of gene expression, which was focused on genes involved in the molecular regulation of MHC class II genes, showed enhancement of pro-apoptotic PCAF and CIITA after the combination of 5-FU and depsipeptide. These results may indicate a closer relationship between elevation of MHC class II expression and cellular apoptosis induced by the combination of depsipeptide and 5-FU. To the best of our knowledge, this is the first study to report that the combination of 5-FU and depsipeptide induces human colon cancer cell apoptosis in a concerted manner with the induction of MHC class II gene expression.
引用
收藏
页码:1875 / 1885
页数:11
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