TY - JOUR
T1 - Cudratricusxanthone G inhibits human colorectal carcinoma cell invasion by MMP-2 down-regulation through suppressing activator protein-1 activity
AU - Kuang, Lisha
AU - Wang, Lei
AU - Wang, Qian
AU - Zhao, Qufei
AU - Du, Bing
AU - Li, Dali
AU - Luo, Jian
AU - Liu, Mingyao
AU - Hou, Aijun
AU - Qian, Min
PY - 2011/5/15
Y1 - 2011/5/15
N2 - Cudratricusxanthone G (CTXG), a natural bioactive cudratricusxanthone extracted from C. tricuspidata, has shown anti-cancer properties. However, the function and mechanism of CTXG in tumor invasion have not been elucidated to date. In this study, we investigated the inhibitory effect of CTXG on the proliferation, migration and invasion of SW620 cells. We found that MMP-2, a pivotal factor in tumor invasion, was suppressed in both expression and activation by CTXG in a dose-dependent manner. The suppression of MMP-2 expression by CTXG led to an inhibition of SW620 cells invasion and migration by inactivating Rac1 and Cdc42 but not RhoA GTPase. Furthermore, CTXG also inhibited the transcriptional activity of AP-1 (activator protein-1). In conclusion, our data demonstrate that CTXG exerted anti-invasion action in SW620 cells by targeting MMP-2 though regulating the activities of Rac1, Cdc42 and their downstream transcriptional factor AP-1. These results are the first to reveal the novel functions of CTXG in cancer cell invasion and its molecular basis for the anti-cancer action.
AB - Cudratricusxanthone G (CTXG), a natural bioactive cudratricusxanthone extracted from C. tricuspidata, has shown anti-cancer properties. However, the function and mechanism of CTXG in tumor invasion have not been elucidated to date. In this study, we investigated the inhibitory effect of CTXG on the proliferation, migration and invasion of SW620 cells. We found that MMP-2, a pivotal factor in tumor invasion, was suppressed in both expression and activation by CTXG in a dose-dependent manner. The suppression of MMP-2 expression by CTXG led to an inhibition of SW620 cells invasion and migration by inactivating Rac1 and Cdc42 but not RhoA GTPase. Furthermore, CTXG also inhibited the transcriptional activity of AP-1 (activator protein-1). In conclusion, our data demonstrate that CTXG exerted anti-invasion action in SW620 cells by targeting MMP-2 though regulating the activities of Rac1, Cdc42 and their downstream transcriptional factor AP-1. These results are the first to reveal the novel functions of CTXG in cancer cell invasion and its molecular basis for the anti-cancer action.
KW - AP-1
KW - Cudratricusxanthone G (CTXG)
KW - Invasion
KW - MMP-2
KW - Rac1
UR - https://www.scopus.com/pages/publications/79955476024
U2 - 10.1016/j.bcp.2011.02.017
DO - 10.1016/j.bcp.2011.02.017
M3 - 文章
C2 - 21377450
AN - SCOPUS:79955476024
SN - 0006-2952
VL - 81
SP - 1192
EP - 1200
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 10
ER -