Butyrate response factor 1 enhances cisplatin sensitivity in human head and neck squamous cell carcinoma cell lines

被引:34
作者
Lee, SK
Kim, SB
Kim, JS
Moon, CH
Han, MS
Lee, BJ
Chung, DK
Min, YJ
Park, JH
Choi, DH
Cho, HR
Park, SK
Park, JW [1 ]
机构
[1] Univ Ulsan, Dept Biol Sci, Ulsan 680749, South Korea
[2] Univ Ulsan, Immunomodulat Res Ctr, Ulsan 680749, South Korea
[3] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Inst Biomed, Ulsan 680749, South Korea
[4] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Internal Med, Ulsan 680749, South Korea
[5] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Surg, Ulsan 680749, South Korea
[6] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Pediat, Ulsan 680749, South Korea
关键词
BRF1; cisplatin; sensitivity; HNSCC;
D O I
10.1002/ijc.21133
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cisplatin is a widely used chemotherapeutic agent in head and neck squamous cell carcinoma (HNSCC). Resistance to cisplatin is a common feature of HNSCC. To identify genes that may regulate cisplatin sensitivity, we carried out a cDNA microarray analysis of gene expression in cisplatin-sensitive and cisplatin-resistant HNSCC-derived cell lines. Among genes differentially expressed by cisplatin treatment, we have confirmed the elevated expression of butyrate responsive factor 1 (BRF1) in cisplatin-sensitive HNSCC cells and have demonstrated that the expression level of BRF1 is associated with cisplatin-sensitivity. Specific inhibition of BRF1 expression using an antisense oligodeoxynucleotide (ODN) decreased the cisplatin-sensitivity and, on the contrary, overexpression of BRF1 increased cisplatin-sensitivity in HNSCC cells. Elevated expression of BRF1 decreased the level of the human inhibitor of apoptosis protein-2 (cIAP2) and increased the caspase-3 activity in HNSCC cells. In addition, elevated expression of BRF1 decreased the expression level of enhanced green fluorescent protein (EGFP) linked to a 3' terminal AU-rich element (ARE) of cIAP2 mRNA. These findings demonstrate that BRF1 expression enhanced cisplatin sensitivity in HNSCC cells by reducing the levels of cIAP2 mRNA. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:32 / 40
页数:9
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