Huang Chin-Shiu, Fan Yang-En, Lin Chen-Yu, Hu Miao-Lin
Department of Food Science and Biotechnology, National Chung-Hsing University, Taichung 402, Taiwan, Republic of China.
J Nutr Biochem. 2007 Jul;18(7):449-56. doi: 10.1016/j.jnutbio.2006.08.007. Epub 2006 Oct 17.
The carotenoid lycopene has been associated with decreased risks of several types of cancer, such as hepatoma. Although lycopene has been shown to inhibit metastasis, its mechanism of action is poorly understood. Here, we used SK-Hep-1 cells (from a human hepatoma) to test whether lycopene exerts its anti-invasion activity via down-regulation of the expression of matrix metalloproteinase (MMP)-9, an important enzyme in the degradation of basement membrane in cancer invasion. The activity and expressions of MMP-9 protein and mRNA were detected by gelatin zymography, Western blotting and RT-PCR, respectively. The binding abilities of nuclear factor-kappa B (NF-kappaB), activator protein-1 and stimulatory protein-1 (Sp1) to the binding sites in the MMP-9 promoter were measured by the electrophoretic mobility shift assay. We showed that lycopene (1-10 microM) significantly inhibited SK-Hep-1 invasion (P<.05) and that this effect correlated with the inhibition of MMP-9 at the levels of enzyme activity (r(2)=.94, P<.001), protein expression (r(2)=.80, P=.007) and mRNA expression (r(2)=.94, P<.001). Lycopene also significantly inhibited the binding abilities of NF-kappaB and Sp1 and decreased, to some extent, the expression of insulin-like growth factor-1 receptor (IGF-1R) and the intracellular level of reactive oxygen species (P<.05). The antioxidant effect of lycopene appeared to play a minor role in its inhibition of MMP-9 and invasion activity of SK-Hep-1 cells because coincubation of cells with lycopene plus hydrogen peroxide abolished the antioxidant effect but did not significantly affect the anti-invasion ability of lycopene. Thus, lycopene decreases the invasive ability of SK-Hep-1 cells by inhibiting MMP-9 expression and suppressing the binding activity of NF-kappaB and Sp1. These effects of lycopene may be related to the down-regulation of IGF-1R, while the antioxidant activity of lycopene appears to play a minor role.
类胡萝卜素番茄红素与多种癌症风险降低有关,如肝癌。尽管已表明番茄红素可抑制转移,但其作用机制尚不清楚。在此,我们使用SK - Hep - 1细胞(来自人肝癌)来测试番茄红素是否通过下调基质金属蛋白酶(MMP)- 9的表达发挥其抗侵袭活性,MMP - 9是癌症侵袭中基底膜降解的一种重要酶。分别通过明胶酶谱法、蛋白质印迹法和逆转录 - 聚合酶链反应检测MMP - 9蛋白和mRNA的活性及表达。通过电泳迁移率变动分析测量核因子 - κB(NF - κB)、活化蛋白 - 1和刺激蛋白 - 1(Sp1)与MMP - 9启动子中结合位点的结合能力。我们发现番茄红素(1 - 10微摩尔)显著抑制SK - Hep - 1细胞侵袭(P <.05),且这种作用与在酶活性水平(r² =.94,P <.001)、蛋白质表达水平(r² =.80,P =.007)和mRNA表达水平(r² =.94,P <.001)对MMP - 9的抑制相关。番茄红素还显著抑制NF - κB和Sp1的结合能力,并在一定程度上降低胰岛素样生长因子 - 1受体(IGF - 1R)的表达和细胞内活性氧水平(P <.05)。番茄红素的抗氧化作用在其对MMP - 9和SK - Hep - 1细胞侵袭活性的抑制中似乎起次要作用,因为细胞与番茄红素加过氧化氢共同孵育消除了抗氧化作用,但并未显著影响番茄红素的抗侵袭能力。因此,番茄红素通过抑制MMP - 9表达和抑制NF - κB及Sp1的结合活性降低SK - Hep - 1细胞的侵袭能力。番茄红素的这些作用可能与IGF - 1R的下调有关,而番茄红素的抗氧化活性似乎起次要作用。