Trillium tschonoskii steroidal saponins suppress the growth of colorectal Cancer cells in vitro and in vivo. (20th June 2015)

• Record Type: Journal Article
• Authors: Li, Yuhua; Liu, Changxu; Xiao, Dan; Han, Jing; Yue, Zhenggang; Sun, Yang; Fan, Lei; Zhang, Feng; Meng, Jin; Zhang, Rong; Wang, Zhipeng; Mei, Qibing; Wen, Aidong
• Is Part Of: Journal of ethnopharmacology. Volume 168(2015)
• Page Start: 136
• Page End: 145
• Publication Date: 2015-06-20
• Subjects: TTS Trillium tschonoskii Steroidal Saponins -- DMH 1, 2-dimethyl-hydrazine -- MTT 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide -- DSS Dextran sodium sulfate -- MAPKs Mitogen-actived protein kinases; Trillium tschonoskii steroidal saponins (TTS) -- Growth inhibition -- Mitogen-actived protein kinases (MAPKs) -- Apoptosis; Ethnopharmacology -- Periodicals; Pharmacognosy -- Periodicals; Herbs -- Periodicals; Herbs -- Periodicals; Pharmacognosy -- Periodicals; Pharmacognosie -- Périodiques; Herbes -- Périodiques; 615.1
• DOI: 10.1016/j.jep.2015.03.063
• Languages: English
• ISSNs: 0378-8741

Abstract

Abstract: Ethnopharmacological relevance: Saponins of many herbs are known to possess anti-cancer effect. Aim of the study: The present study aimed to investigate the growth inhibitory effect of Trillium tschonoskii steroidal saponins in a mouse model of colitis-associated colorectal cancer and a human colorectal cancer cell line HT-29, and isolate some major constituents and evaluate their anti-tumor activity. Materials and methods: Forty male ICR mice were administered with 1, 2-dimethyl-hydrazine (DMH) and dextran sodium sulfate (DSS). Ten mice were given no further treatment, the rest were administered with different doses of TTS (5, 10, 20 mg/kg) orally, every three days from the 9th week to the 20th week. Results: TTS effectively protected ICR mice against DMH/DSS-induced tumorigenesis. The incidence of tumor development was 90% (9/10) in the mice treated with DMH/DSS, but that was reduced to 50% (5/10), 40% (4/10), and 20% (2/10), respectively, in the mice treated with 5%, 10%, and 20% of TTS. Results of Ki-67 staining, TUNEL assay and caspase-3 activity assay revealed that TTS moderately decreased abnormal proliferation and increased apoptosis of colonic epithelial cells. It inhibited the growth and triggered the apoptosis of HT-29 cells, partly through suppressing mitogen-actived protein kinases (MAPKs) and triggering mitochondrial-mediated apoptotic pathway. Three compounds, namely, Paris saponin VII, polyphylloside III and Paris saponin VI, were important active compounds in TTS. Conclusion: These data suggest that TTS has a potential role in clinical prevention and treatment for colorectal cancer. Graphical abstract: