Curcumin inhibits tumor growth and angiogenesis in glioblastoma xenografts

被引:163
作者
Perry, Marie-Claude [1 ]
Demeule, Michel [1 ]
Regina, Anthony [1 ]
Moumdjian, Robert [2 ]
Beliveau, Richard [1 ]
机构
[1] Univ Quebec, Hop St Justine, Mol Med Lab, Montreal, PQ H3C 3P8, Canada
[2] Hop Notre Dame de Bon Secours, Dept Neurochirurg, Montreal, PQ H2L 4K8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Anti-angiogenic; Anti-tumor; Blood-brain barrier; Curcumin; Glioblastoma; IN-VITRO; CELLS; EXPRESSION; MANAGEMENT; VIVO;
D O I
10.1002/mnfr.200900277
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
Among the natural products shown to possess chemopreventive and anticancer properties, curcumin is one of the most potent. In the current study, we investigated the effects of this natural product on the growth of human glioma U-87 cells xenografted into athymic mice. We show here that curcumin administration exerted significant anti-tumor effects on subcutaneous and intracerebral gliomas as demonstrated by the slower tumor growth rate and the increase of animal survival time. While investigating the mechanism of its action in vivo, we observed that curcumin decreased the gelatinolytic activities of matrix metalloproteinase-9. Furthermore, treatment with curcumin inhibited glioma-induced angiogenesis as indicated by the decrease of endothelial cell marker from newly formed vessels and by the diminution of the concentration of hemoglobin in curcumin-treaded tumors. We also demonstrate, using an in vitro model of blood-brain barrier, that curcumin can cross the blood-brain barrier to a high level. These are the first results showing that curcumin suppresses tumor growth of gliomas in xenograft models. The mechanisms of the anti-tumor effects of curcumin were related, at least partly, to the inhibition of glioma-induced angiogenesis.
引用
收藏
页码:1192 / 1201
页数:10
相关论文
共 29 条
[1]
Curcumin is an in vivo inhibitor of angiogenesis [J].
Arbiser, JL ;
Klauber, N ;
Rohan, R ;
van Leeuwen, R ;
Huang, MT ;
Fisher, C ;
Flynn, E ;
Byers, HR .
MOLECULAR MEDICINE, 1998, 4 (06) :376-383
[2]
Bian XW, 2000, ANAL QUANT CYTOL, V22, P267
[3]
In vitro model for evaluating drug transport across the blood-brain barrier [J].
Cecchelli, R ;
Dehouck, B ;
Descamps, L ;
Fenart, L ;
Buée-Scherrer, V ;
Duhem, C ;
Lundquist, S ;
Rentfel, M ;
Torpier, G ;
Dehouck, MP .
ADVANCED DRUG DELIVERY REVIEWS, 1999, 36 (2-3) :165-178
[4]
Cheng AL, 2001, ANTICANCER RES, V21, P2895
[5]
Matrix metalloproteinases and their biological function in human gliomas [J].
Chintala, SK ;
Tonn, JC ;
Rao, JS .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 1999, 17 (5-6) :495-502
[6]
de Vries Nienke A, 2006, Expert Rev Neurother, V6, P1199, DOI 10.1586/14737175.6.8.1199
[7]
Matrix metalloproteinase inhibition by green tea catechins [J].
Demeule, M ;
Brossard, M ;
Pagé, M ;
Gingras, D ;
Béliveau, R .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1478 (01) :51-60
[8]
Chemopreventive and therapeutic effects of curcumin [J].
Duvoix, A ;
Blasius, R ;
Delhalle, S ;
Schnekenburger, M ;
Morceau, F ;
Henry, E ;
Dicato, M ;
Diederich, M .
CANCER LETTERS, 2005, 223 (02) :181-190
[9]
Elattar TMA, 2000, ANTICANCER RES, V20, P1733
[10]
ElHafny B, 1996, J CELL PHYSIOL, V167, P451, DOI 10.1002/(SICI)1097-4652(199606)167:3<451::AID-JCP9>3.0.CO