Ginkgo biloba extracts and cancer:: a research area in its infancy

被引:170
作者
DeFeudis, FV
Papadopoulos, V
Drieu, K
机构
[1] Inst Biosci, Westborough, MA USA
[2] Georgetown Univ, Med Ctr, Div Hormone Res, Dept Cell Biol, Washington, DC USA
[3] Georgetown Univ, Med Ctr, Div Hormone Res, Dept Pharmacol, Washington, DC USA
[4] Georgetown Univ, Med Ctr, Lombardi Canc Ctr, Washington, DC USA
[5] Beafour IPSEN Pharma, Paris, France
关键词
antioxidant; cancer; chemoprevention; gene expression; Ginkgo biloba; ginkgolide;
D O I
10.1046/j.1472-8206.2003.00156.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recent studies conducted with various molecular, cellular and whole animal models have revealed that leaf extracts of Ginkgo biloba may have anticancer (chemopreventive) properties that are related to their antioxidant, anti-angiogenic and gene-regulatory actions. The antioxidant and associated anti-lipoperoxidative effects of Ginkgo extracts appear to involve both their flavonoid and terpenoid constituents. The anti-angiogenic activity of the extracts may involve their antioxidant activity and their ability to inhibit both inducible and endothelial forms of nitric oxide synthase. With regard to gene expression, a Ginkgo extract and one of its terpenoid constituents, ginkgolide B, inhibited the proliferation of a highly aggressive human breast cancer cell line and xenografts of this cell line in nude mice. cDNA microarray analyses have shown that exposure of human breast cancer cells to a Ginkgo extract altered the expression of genes that are involved in the regulation of cell proliferation, cell differentiation or apoptosis, and that exposure of human bladder cancer cells to a Ginkgo extract produced an adaptive transcriptional response that augments antioxidant status and inhibits DNA damage. In humans, Ginkgo extracts inhibit the formation of radiation-induced (chromosome-damaging) clastogenic factors and ultraviolet light-induced oxidative stress - effects that may also be associated with anticancer activity. Flavonoid and terpenoid constituents of Ginkgo extracts may act in a complementary manner to inhibit several carcinogenesis-related processes, and therefore the total extracts may be required for producing optimal effects.
引用
收藏
页码:405 / 417
页数:13
相关论文
共 110 条
[1]  
Agha AM, 2001, J EXP CLIN CANC RES, V20, P39
[2]  
[Anonymous], 1998, GINKGO BILOBA EXTRAC
[3]   Inhibition of caspase proteases by CrmA enhances the resistance of human leukemic cells to multiple chemotherapeutic agents [J].
Antoku, K ;
Liu, Z ;
Johnson, DE .
LEUKEMIA, 1997, 11 (10) :1665-1672
[4]   PARP-mediated proteasome activation: a co-ordination of DNA repair and protein degradation? [J].
Arnold, J ;
Grune, T .
BIOESSAYS, 2002, 24 (11) :1060-1065
[5]  
Batra S, 1998, INT J ONCOL, V12, P1295
[6]   IMAGING OF HUMAN-BRAIN LESIONS WITH AN OMEGA-3 SITE RADIOLIGAND [J].
BENAVIDES, J ;
CORNU, P ;
DENNIS, T ;
DUBOIS, A ;
HAUW, JJ ;
MACKENZIE, ET ;
SAZDOVITCH, V ;
SCATTON, B .
ANNALS OF NEUROLOGY, 1988, 24 (06) :708-712
[7]   The role of mast cell tryptase in neoangiogenesis of premalignant and malignant lesions of the uterine cervix [J].
Benítez-Bribiesca, L ;
Wong, A ;
Utrera, D ;
Castellanos, E .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2001, 49 (08) :1061-1062
[8]   MAP kinases and hypoxia in the control of VEGF expression [J].
Berra, E ;
Pagès, G ;
Pouysségur, J .
CANCER AND METASTASIS REVIEWS, 2000, 19 (1-2) :139-145
[9]   CHEMOPREVENTIVE EFFICACY OF A BETEL LEAF EXTRACT AGAINST BENZO[A]PYRENE-INDUCED FORESTOMACH TUMORS IN MICE [J].
BHIDE, SV ;
ZARIWALA, MBA ;
AMONKAR, AJ ;
AZUINE, MA .
JOURNAL OF ETHNOPHARMACOLOGY, 1991, 34 (2-3) :207-213
[10]   Location-dependent role of the human glioma cell peripheral-type benzodiazepine receptor in proliferation and steroid biosynthesis [J].
Brown, RC ;
Degenhardt, B ;
Kotoula, M ;
Papadopoulous, V .
CANCER LETTERS, 2000, 156 (02) :125-132