Deltonin, a Steroidal Saponin, Inhibits Colon Cancer Cell Growth in Vitro and Tumor Growth in Vivo via Induction of Apoptosis and Antiangiogenesis

被引:31
作者
Tong, Qing-Yi
Qing, Yong
Shu, Dan
He, Yang
Zhao, Ying-Lan
Li, Yi
Wang, Zhen-Ling
Zhang, Shi-Yuan
Xing, Zhi-hua
Xu, Cheng
Wei, Yu-Quan
Huang, Wen
Wu, Xiao-Hua
机构
[1] W China Hosp, Regenerat Med Res Ctr, Lab Ethnopharmacol, Chengdu, Peoples R China
[2] W China Hosp, State Key Lab Biotherapy, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
Steroidal saponin; Deltonin; Anti-tumor; Colorectal Cancer; Apoptosis; Antiangiogenesis; FLUOROURACIL PLUS LEUCOVORIN; METASTATIC COLORECTAL-CANCER; C; H; WRIGHT; ORAL CAPECITABINE; ANGIOGENESIS; PROLIFERATION; ACTIVATION; EXPRESSION; DEATH;
D O I
10.1159/000327949
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Deltonin, a steroidal saponin, isolated from Dioscorea zingiberensis Wright (DZW), has shown high-cytotoxic activity in cancer cells. However, its mechanisms and in vivo anti-cancer effects remain unknown. In the present study, we evaluated the effects and explored the anti-tumor mechanisms of deltonin on a panel of colon cancer cell lines and in a mouse model of murine colon cancer C26. Deltonin had more cytotoxic effect on C26 cells than 5-fluorouracil had, promoting dramatic G2-M phase arrest and apoptosis in C26 cells in a concentration-dependent manner; oral administration of deltonin significantly inhibited the tumor growth and prolonged survival of the tumor bearing mice. The deltonin treatment caused a noticeable apoptosis in tumor tissue, which associated with increased levels of Bax, activated caspase-3, caspase-9, and cleaved poly (ADPribose) polymerase, decreased pro-caspase-8, pro-caspase-9, Bcl-2 expression levels and extracellular signal regulated kinase-1/2 activity; and dose-dependently inhibit angiogenesis. In conclusion, the findings in this study demonstrated that deltonin is an effective natural agent for cancer therapy, which may be mediated, in part, by induction of apoptosis, as well as involve mitogen-activated protein kinase pathways, and inhibition of angiogenesis. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:233 / 242
页数:10
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