TY - JOUR
T1 - Anti-angiogenic activity of acalycixenolide E, a novel marine natural product from Acalycigorgia inermis
AU - Kwon, H. J.
AU - Kim, J. H.
AU - Jung, H. J.
AU - Kwon, Y. G.
AU - Kim, M. Y.
AU - Rho, J. R.
AU - Shin, J.
PY - 2001
Y1 - 2001
N2 - Angiogenesis is known as a crucial process in the growth and spreading of tumor cells. Accordingly, the effective inhibition of this process would appear to be a promising way to cure angiogenesis-related diseases, including cancer. This study demonstrates that acalycixenolide E (AX-E) from the marine organism Acalycigorgia inermis exhibits a potent anti-angiogenic activity both in vitro and in vivo. AX-E inhibits the bFGF-induced proliferation of HUVECs in a dose dependent manner, along with the bFGF-induced migration, invasion, and tube formation of HUVECs. Moreover, AX-E potently inhibits the in vivo neovascularization of the chorioallantoic membranes (CAMs) of growing chick embryos. Interestingly, AX-E suppresses the expression of metalloproteases 2 and 9, yet shows no effect on their activities. The novel chemical structure and potent anti-angiogenic activity of AX-E will be of great value in elucidating the molecular mechanism of angiogenesis as well as in the development of a novel anti-angiogenic drug.
AB - Angiogenesis is known as a crucial process in the growth and spreading of tumor cells. Accordingly, the effective inhibition of this process would appear to be a promising way to cure angiogenesis-related diseases, including cancer. This study demonstrates that acalycixenolide E (AX-E) from the marine organism Acalycigorgia inermis exhibits a potent anti-angiogenic activity both in vitro and in vivo. AX-E inhibits the bFGF-induced proliferation of HUVECs in a dose dependent manner, along with the bFGF-induced migration, invasion, and tube formation of HUVECs. Moreover, AX-E potently inhibits the in vivo neovascularization of the chorioallantoic membranes (CAMs) of growing chick embryos. Interestingly, AX-E suppresses the expression of metalloproteases 2 and 9, yet shows no effect on their activities. The novel chemical structure and potent anti-angiogenic activity of AX-E will be of great value in elucidating the molecular mechanism of angiogenesis as well as in the development of a novel anti-angiogenic drug.
UR - http://www.scopus.com/inward/record.url?scp=0034802235&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034802235&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0034802235
SN - 1017-7825
VL - 11
SP - 656
EP - 662
JO - Journal of microbiology and biotechnology
JF - Journal of microbiology and biotechnology
IS - 4
ER -