A small-molecule metastasis inhibitor, norcantharidin, downregulates matrix metalloproteinase-9 expression by inhibiting Sp1 transcriptional activity in colorectal cancer cells

被引:104
作者
Chen, Yu-Jen [3 ]
Chang, Wei-Min [4 ]
Liu, Yi-Wen [4 ]
Lee, Chia-Yun [2 ]
Jang, Yi-Hua [2 ]
Kuo, Cheng-Deng [1 ]
Liao, Hui-Fen [1 ,2 ]
机构
[1] Taipei Vet Gen Hosp, Dept Med Res & Educ, Taipei 112, Taiwan
[2] Natl Chiayi Univ, Dept Biochem Sci & Technol, Chiayi 600, Taiwan
[3] Mackay Mem Hosp, Dept Radiat Oncol, Taipei 104, Taiwan
[4] Natl Chiayi Univ, Grad Inst Biomed & Biopharmaceut Sci, Chiayi 600, Taiwan
关键词
Norcantharidin; Matrix metalloproteinase-9 (MMP-9); Sp1; Colorectal cancer; GENE-EXPRESSION; ANTICANCER ACTIVITY; KAPPA-B; APOPTOSIS; MMP-9; STAT-1-ALPHA; ACTIVATION; MECHANISMS; HEPATOMA; GAMMA;
D O I
10.1016/j.cbi.2009.07.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Norcantharidin (NCTD) is a small-molecule metastasis inhibitor without renal toxicity derived from a renal toxic compound cantharidin, which is found in blister beetles (Mylabris phalerata Pall.). commonly used in traditional Chinese medicine. The anti-metastatic capacity of NCTD is apparently through the downexpression of matrix metalloproteinase-9 (MMP-9) activity. The aim of this study was to clarify the transcriptional regulation of MMP-9 gene by NCTD in colorectal cancer CT-26 cells. NCTD not only down-regulated MMP-9 mRNA and protein expression, but also inhibited gelatinase activity in a concentration- and time-dependent manner. In CT26 cells with transfection of cis-element reporter plasmids, NCTD treatment decreased reporter luciferase activity from a Sp1 construct, augmented with a NF-kappa B construct, but this did not occur with an AP-1 construct. Further transfecting with constructs containing wild-type or various mutant MMP-9 promoters in CT26 cells indicated that Sp1, but not the others, was required for NCTD-inhibition of MMP-9 promoter transactivation. More evidence by electrophoretic mobility shift assay demonstrated that NCTD inhibited the DNA-binding activity of Sp1. In addition, the increase effect of NF-kappa B-luciferase activity by NCTD may include the upexpression of nuclear STAT and result in competitive suppression of NF-kappa B-binding activity in MMP-9 promoter. In conclusion. the metastasis inhibitor NCTD downregulates MMP-9 expression by inhibiting Sp1 transcriptional activity in colorectal cancer CT26 cells. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:440 / 446
页数:7
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