Cha H J, Bae S K, Lee H Y, Lee O H, Sato H, Seiki M, Park B C, Kim K W
Department of Molecular Biology, Pusan National University, Korea.
Cancer Res. 1996 May 15;56(10):2281-4.
We examined the anti-invasive activity of ursolic acid (UA) on the highly metastatic HT1080 human fibrosarcoma cell line. UA reduced tumor cell invasion through a reconstituted basement membrane in a transwell chamber. A significant down-regulation of matrix metalloproteinase-9 [MMP-9; Mr 92,000 gelatinase/type IV collagenase (gelatinase B)] by UA was detected by Northern blot analysis. However, MMP-2 [Mr 72,000 gelatinase/type IV collagenase (gelatinase A)] and membrane-type MMP were constantly expressed, and the expression of tissue inhibitor of metalloproteinase (TIMP)-1 and TIMP-2 also was not changed after 3 and 6 days of treatment with UA. Quantitative gelatin-based zymography confirmed a markedly reduced expression of MMP-9 but not MMP-2 after treatment with UA. To confirm the UA-induced down-regulation of MMP-9 expression, we constructed a secreted alkaline phosphatase (SEAP) reporter vector including MMP-9 promoter. After transfection of MMP-9/SEAP reporter vector into HT1080 cells, reduced SEAP activity was detected after treatment with UA. These results suggest that down-regulation of MMP-9 contributes to the anti-invasive activity of UA in HT1080 cells.
我们检测了熊果酸(UA)对高转移性HT1080人纤维肉瘤细胞系的抗侵袭活性。UA减少了肿瘤细胞通过Transwell小室中重组基底膜的侵袭。通过Northern印迹分析检测到UA显著下调基质金属蛋白酶-9 [MMP-9;分子量92,000的明胶酶/IV型胶原酶(明胶酶B)]。然而,MMP-2 [分子量72,000的明胶酶/IV型胶原酶(明胶酶A)]和膜型MMP持续表达,并且在用UA处理3天和6天后,金属蛋白酶组织抑制剂(TIMP)-1和TIMP-2的表达也未改变。基于明胶的定量酶谱分析证实,用UA处理后MMP-9的表达明显降低,但MMP-2未降低。为了证实UA诱导的MMP-9表达下调,我们构建了一个包含MMP-9启动子的分泌型碱性磷酸酶(SEAP)报告载体。将MMP-9/SEAP报告载体转染到HT1080细胞中后,用UA处理后检测到SEAP活性降低。这些结果表明,MMP-9的下调有助于UA对HT1080细胞的抗侵袭活性。