The neem limonoids azadirachtin and nimbolide inhibit hamster cheek pouch carcinogenesis by modulating xenobiotic-metabolizing enzymes, DNA damage, antioxidants, invasion and angiogenesis

被引:79
作者
Priyadarsini, Ramamurthi Vidya [1 ]
Manikandan, Palrasu [1 ]
Kumar, Gurram Harish [1 ]
Nagini, Siddavaram [1 ]
机构
[1] Annamalai Univ, Dept Biochem & Biotechnol, Fac Sci, Annamalainagar 608002, Tamil Nadu, India
关键词
Angiogenesis; antioxidants; azadirachtin; DMBA; invasion; neem; nimbolide; xenobiotic-metabolizing enzymes; EXPERIMENTAL ORAL CARCINOGENESIS; ENDOTHELIAL GROWTH-FACTOR; BLACK TEA POLYPHENOLS; CANCER-THERAPY; LEAF EXTRACT; CHEMICAL CARCINOGENESIS; GLUTATHIONE PEROXIDASE; CELL-LINES; IN-VIVO; INDICA;
D O I
10.1080/10715760902870637
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The neem tree has attracted considerable research attention as a rich source of limonoids that have potent antioxidant and anti-cancer properties. The present study was designed to evaluate the chemopreventive potential of the neem limonoids azadirachtin and nimbolide based on in vitro antioxidant assays and in vivo inhibitory effects on 7,12-dimethylbenz[a]anthracene (DMBA)-induced hamster buccal pouch (HBP) carcinogenesis. Both azadirachtin and nimbolide exhibited concentration-dependent anti-radical scavenging activity and reductive potential in the order: nimbolide azadirachtin ascorbate. Administration of both azadirachtin and nimbolide inhibited the development of DMBA-induced HBP carcinomas by influencing multiple mechanisms including prevention of procarcinogen activation and oxidative DNA damage, upregulation of antioxidant and carcinogen detoxification enzymes and inhibition of tumour invasion and angiogenesis. On a comparative basis, nimbolide was found to be a more potent antioxidant and chemopreventive agent and offers promise as a candidate agent in multitargeted prevention and treatment of cancer.
引用
收藏
页码:492 / 504
页数:13
相关论文
共 53 条
[1]
Cytotoxicity of azadirachtin A in human glioblastoma cell lines [J].
Akudugu, J ;
Gäde, G ;
Böhm, L .
LIFE SCIENCES, 2001, 68 (10) :1153-1160
[2]
CARCINOGENS ARE MUTAGENS - SIMPLE TEST SYSTEM COMBINING LIVER HOMOGENATES FOR ACTIVATION AND BACTERIA FOR DETECTION [J].
AMES, BN ;
DURSTON, WE ;
YAMASAKI, E ;
LEE, FD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (08) :2281-2285
[3]
ANDERSON ME, 1985, METHOD ENZYMOL, V113, P548
[4]
Role of PIGF in the intra- and intermolecular cross talk between the VEGF receptors Flt1 and Flk1 [J].
Autiero, M ;
Waltenberger, J ;
Communi, D ;
Kranz, A ;
Moons, L ;
Lambrechts, D ;
Kroll, J ;
Plaisance, S ;
De Mol, M ;
Bono, F ;
Kliche, S ;
Fellbrich, G ;
Ballmer-Hofer, K ;
Maglione, D ;
Mayr-Beyrle, U ;
Dewerchin, M ;
Dombrowski, S ;
Stanimirovic, D ;
Van Hummelen, P ;
Dehio, C ;
Hicklin, DJ ;
Persico, G ;
Herbert, JM ;
Communi, D ;
Shibuya, M ;
Collen, D ;
Conway, EM ;
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (07) :936-943
[5]
ANTIOXIDANT DETERMINATIONS BY THE USE OF A STABLE FREE RADICAL [J].
BLOIS, MS .
NATURE, 1958, 181 (4617) :1199-1200
[6]
Neem leaf preparation induces apoptosis of tumor cells by releasing cytotoxic Cytokines from human peripheral blood mononuclear cells [J].
Bose, Anamika ;
Haque, Enamul ;
Baral, Rathindranath .
PHYTOTHERAPY RESEARCH, 2007, 21 (10) :914-920
[7]
ETHOXYPHENOXAZONES, PENTOXYPHENOXAZONES, AND BENZYLOXYPHENOXAZONES AND HOMOLOGS - A SERIES OF SUBSTRATES TO DISTINGUISH BETWEEN DIFFERENT INDUCED CYTOCHROMES-P-450 [J].
BURKE, MD ;
THOMPSON, S ;
ELCOMBE, CR ;
HALPERT, J ;
HAAPARANTA, T ;
MAYER, RT .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (18) :3337-3345
[8]
Histone deacetylase inhibitors: Mechanisms of cell death and promise in combination cancer therapy [J].
Carew, Jennifer S. ;
Giles, Francis J. ;
Nawrocki, Steffan T. .
CANCER LETTERS, 2008, 269 (01) :7-17
[9]
CARLBERG I, 1985, METHOD ENZYMOL, V113, P484
[10]
Synergism between vascular endothelial growth factor and placental growth factor contributes to angiogenesis and plasma extravasation in pathological conditions [J].
Carmeliet, P ;
Moons, L ;
Luttun, A ;
Vincenti, V ;
Compernolle, V ;
De Mol, M ;
Wu, Y ;
Bon, F ;
Devy, L ;
Beck, H ;
Scholz, D ;
Acker, T ;
DiPalma, T ;
Dewerchin, M ;
Noel, A ;
Stalmans, I ;
Barra, A ;
Blacher, S ;
Vandendriessche, T ;
Ponten, A ;
Eriksson, U ;
Plate, KH ;
Foidart, JM ;
Schaper, W ;
Charnock-Jones, DS ;
Hicklin, DJ ;
Herbert, JM ;
Collen, D ;
Persico, MG .
NATURE MEDICINE, 2001, 7 (05) :575-583