Lee Kyung Jin, Hwang Soo Jin, Choi Jae Ho, Jeong Hye Gwang
BK21 Project Team, Department of Pharmacy, College of Pharmacy, Research Center for Proteinous Materials, Chosun University, Gwangju, South Korea.
Cancer Lett. 2008 Sep 18;268(2):233-43. doi: 10.1016/j.canlet.2008.03.058. Epub 2008 May 21.
The chemopreventive effects of saponin derived from Platycodon grandiflorum (Changkil saponin; CKS) on tumor invasion and migration and the possible mechanisms involved in this protection were investigated in HT-1080 tumor cells. In this study, we found that CKS reduced 12-O-tetradecanoylphorbol-13-acetate (PMA)-enhanced Matrix metalloproteinases (MMP)-9 and MMP-2 activation in a dose-dependant manner and further inhibited HT-1080 cell invasion and migration. In addition, CKS suppressed PMA-enhanced expression of MMP-9 protein, mRNA and transcription activity levels through suppression of nuclear factor (NF)-kappaB activation without changing tissue inhibitor of metalloproteinase (TIMP)-1 level. CKS also reduced PMA-enhanced MMP-2 active forms through suppression of membrane-type 1 MMP (MT1-MMP) level, but did not alter MMP-2 and TIMP-2 levels. Moreover, reactive oxygen species (ROS) production induced by PMA was partly decreased in the presence of CKS and this suppression of ROS production may be related to diminish NF-kappaB activity. Therefore, our results suggested that the inhibitory effects of CKS on MMP-2 and MMP-9 activation, relation of tumor invasion and migration in vitro possibly involve mechanisms related to its ability to suppress PMA-enhanced NF-kappaB activation through ROS signaling pathway. Overall, CKS may be a valuable anti-invasive drug candidate for cancer therapy.
研究了桔梗皂苷(长基皂苷;CKS)对HT - 1080肿瘤细胞肿瘤侵袭和迁移的化学预防作用及其可能的保护机制。在本研究中,我们发现CKS以剂量依赖性方式降低了12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(PMA)增强的基质金属蛋白酶(MMP)- 9和MMP - 2的激活,并进一步抑制了HT - 1080细胞的侵袭和迁移。此外,CKS通过抑制核因子(NF)-κB的激活,在不改变金属蛋白酶组织抑制剂(TIMP)- 1水平的情况下,抑制了PMA增强的MMP - 9蛋白、mRNA和转录活性水平。CKS还通过抑制膜型1 MMP(MT1 - MMP)水平降低了PMA增强的MMP - 2活性形式,但未改变MMP - 2和TIMP - 2水平。此外,在存在CKS的情况下,PMA诱导的活性氧(ROS)产生部分降低,这种对ROS产生的抑制可能与NF - κB活性的降低有关。因此,我们的结果表明,CKS对MMP - 2和MMP - 9激活的抑制作用,以及在体外对肿瘤侵袭和迁移的抑制作用,可能涉及其通过ROS信号通路抑制PMA增强的NF - κB激活的能力。总体而言,CKS可能是一种有价值的癌症治疗抗侵袭药物候选物。