Background: Tumor metastases are the main reasons for oncotherapy failure. Paris polyphylla (Chinese name:Chonglou) has traditionally been used for its anti-cancer actions. In this article, we focus on the regulation ofhuman lung cancer A549 cell metastases and invasion by Paris polyphylla steroidal saponins (PPSS). Materialsand Methods: Cell viability was evaluated in A549 cells by MTT assay. Effects of PPSS on invasion and migrationwere investigated by wound-healing and matrigel invasion chamber assays. Adhesion to type IV collagen andlaminin was evaluated by MTT assay. Expression and protease activity of two matrix metalloproteinases (MMPs),MMP-2 and MMP-9, were analyzed by Western blotting and gelatin zymography, respectively. Results: PPSSexerted growth inhibitory effects on A549 cells, and effectively inhibited A549 cell adhesion, migration andinvasion in a concentration-dependent manner. Western blotting and gelatin zymography analysis revealed thatPPSS inhibited the expression and secretion of MMP-2 and MMP-9 in A549 cells. Conclusions: PPSS has thepotential to suppress the migration, adhesion and invasion of A549 cells. PPSS could be a potential candidatefor interventions against lung cancer metastases.
(2014). Steroidal Saponins from Paris polyphylla Suppress Adhesion, Migration and Invasion of Human Lung Cancer A549 Cells Via Down-Regulating MMP-2 and MMP-9. Asian Pacific Journal of Cancer Prevention, 15(24), 10911-10916.
MLA
. "Steroidal Saponins from Paris polyphylla Suppress Adhesion, Migration and Invasion of Human Lung Cancer A549 Cells Via Down-Regulating MMP-2 and MMP-9". Asian Pacific Journal of Cancer Prevention, 15, 24, 2014, 10911-10916.
HARVARD
(2014). 'Steroidal Saponins from Paris polyphylla Suppress Adhesion, Migration and Invasion of Human Lung Cancer A549 Cells Via Down-Regulating MMP-2 and MMP-9', Asian Pacific Journal of Cancer Prevention, 15(24), pp. 10911-10916.
VANCOUVER
Steroidal Saponins from Paris polyphylla Suppress Adhesion, Migration and Invasion of Human Lung Cancer A549 Cells Via Down-Regulating MMP-2 and MMP-9. Asian Pacific Journal of Cancer Prevention, 2014; 15(24): 10911-10916.