Antitumor activity of SK-7041, a novel histone deacetylase inhibitor, in human lung and breast cancer cells

被引:0
|
作者
Lee, Keun-Wook
Kim, Jee Hyun
Park, Jung-Hyun
Kim, Hwang-Phill
Song, Sang-Hyun
Kim, Sang Gyun
Kim, Tai Young
Jong, Hyun-Soon
Jung, Kyung Hae
Im, Seock-Ah
Kim, Tae-You
Kim, Noe Kyeong
Bang, Yung-Jue
机构
[1] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110744, South Korea
[3] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, Songnam, South Korea
[4] Seoul Natl Univ Hosp, Dept Internal Med, Seoul 110744, South Korea
[5] Natl Canc Ctr, Res Inst Hosp, Goyang 411769, Gyeonggi, South Korea
关键词
SK-7041; histone deacetylase inhibitor; lung cancer; breast cancer; apoptosis;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A class of synthetic histone deacetylase (HDAC) inhibitors, which are hybrids of trichostatin A and MS-275 were previously developed. In this study, the antitumor effects of SK-7041, one of those novel HDAC inhibitors, was evaluated on lung and breast cancer cell lines. Materials and Methods: Human lung and breast cancer cells, as well as normal human bronchial epithelial (NHBE) cells were treated with SK-7041, and results were compared with those of cells treated with suberoylanilide hydroxamic acid (SAHA). Results: SK-7041 induced time-dependent histone hyperacetylation and showed more potent cytotoxicity than SAHA in cancer cells. These antiproliferative effects of SK-7041 were due to apoptotic cell death caused by G21M-phase arrest and to a lesser extent to G1 arrest. Moreover, SK-7041 inhibited cancer cell proliferation more selectively than NHBE cell proliferation. Conclusion: These results suggest that SK-7041 may have potential anticancer activity.
引用
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页码:3429 / 3438
页数:10
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