TY - JOUR
T1 - Dauricine induces apoptosis, inhibits proliferation and invasion through inhibiting NF-κB signaling pathway in colon cancer cells
AU - Yang, Zhengfeng
AU - Li, Chenghai
AU - Wang, Xiu
AU - Zhai, Chunyan
AU - Yi, Zhengfang
AU - Wang, Lei
AU - Liu, Bisheng
AU - Du, Bing
AU - Wu, Huihui
AU - Guo, Xizhi
AU - Liu, Mingyao
AU - Li, Dali
AU - Luo, Jian
PY - 2010/10
Y1 - 2010/10
N2 - Dauricine, a bioactive component of Asiatic Moonseed Rhizome, has been widely used to treat a large number of inflammatory diseases in traditional Chinese medicine. In our study, we demonstrated that dauricine inhibited colon cancer cell proliferation and invasion, and induced apoptosis by suppressing nuclear factor-kappaB (NF-κB) activation in a dose- and time-dependent manner. Addition of dauricine inhibited the phosphorylation and degradation of IκBα, and the phosphorylation and translocation of p65. Moreover, dauricine down-regulated the expression of various NF-κB-regulated genes, including genes involved cell proliferation (cyclinD1, COX2, and c-Myc), anti-apoptosis (survivin, Bcl-2, XIAP, and IAP1), invasion (MMP-9 and ICAM-1), and angiogenesis (VEGF). In athymic nu/nu mouse model, we further demonstrated that dauricine significantly suppressed colonic tumor growth. Taken together, our results demonstrated that dauricine inhibited colon cancer cell proliferation, invasion, and induced cell apoptosis by suppressing NF-κB activity and the expression profile of its downstream genes. These findings provide evidence for a novel role of dauricine in preventing or treating colon cancer through modulation of NF-κB singling pathway.
AB - Dauricine, a bioactive component of Asiatic Moonseed Rhizome, has been widely used to treat a large number of inflammatory diseases in traditional Chinese medicine. In our study, we demonstrated that dauricine inhibited colon cancer cell proliferation and invasion, and induced apoptosis by suppressing nuclear factor-kappaB (NF-κB) activation in a dose- and time-dependent manner. Addition of dauricine inhibited the phosphorylation and degradation of IκBα, and the phosphorylation and translocation of p65. Moreover, dauricine down-regulated the expression of various NF-κB-regulated genes, including genes involved cell proliferation (cyclinD1, COX2, and c-Myc), anti-apoptosis (survivin, Bcl-2, XIAP, and IAP1), invasion (MMP-9 and ICAM-1), and angiogenesis (VEGF). In athymic nu/nu mouse model, we further demonstrated that dauricine significantly suppressed colonic tumor growth. Taken together, our results demonstrated that dauricine inhibited colon cancer cell proliferation, invasion, and induced cell apoptosis by suppressing NF-κB activity and the expression profile of its downstream genes. These findings provide evidence for a novel role of dauricine in preventing or treating colon cancer through modulation of NF-κB singling pathway.
UR - https://www.scopus.com/pages/publications/77956501287
U2 - 10.1002/jcp.22261
DO - 10.1002/jcp.22261
M3 - 文章
C2 - 20509140
AN - SCOPUS:77956501287
SN - 0021-9541
VL - 225
SP - 266
EP - 275
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 1
ER -