Antioxidant activities of novel resveratrol analogs in breast cancer

被引:23
作者
Chatterjee, Anwesha [1 ]
Ronghe, Amruta [1 ]
Padhye, Subhash B. [2 ]
Spade, David A. [3 ]
Bhat, Nimee K. [1 ]
Bhat, Hari K. [1 ]
机构
[1] Univ Missouri, Sch Pharm, Div Pharmacol & Toxicol, Kansas City, MO 64108 USA
[2] Univ Pune, Interdisciplinary Sci & Technol Res Acad, Dept Chem, Abeda Inamdar Senior Coll, Pune, Maharashtra, India
[3] Univ Missouri, Dept Math & Stat, Kansas City, MO 64110 USA
关键词
antioxidant properties; breast cancer; HPIMBD; oxidative stress; resveratrol; resveratrol analogs; TIMBD; OXIDATIVE DNA-DAMAGE; ELEMENT-MEDIATED EXPRESSION; SYRIAN-HAMSTERS; ESTROGEN; STRESS; INDUCTION; CARCINOGENESIS; INHIBITION; STATISTICS; MECHANISMS;
D O I
10.1002/jbt.21925
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The objective of the present study was to characterize the role of novel resveratrol (Res) analogs: 4-(E)-{(4-hydroxyphenylimino)-methylbenzene, 1, 2-diol} (HPIMBD) and 4-(E)-{(p-tolylimino)-methylbenzene-1,2-diol} (TIMBD) as potent antioxidants against breast cancer. Non-neoplastic breast epithelial cell lines MCF-10A and MCF-10F were treated with 17-estradiol (E2), Res, HPIMBD, and TIMBD for up to 72h. mRNA and protein levels of antioxidant genes, superoxide dismutase 3 (SOD3) and N-quinoneoxidoreductase-1 (NQO1) and transcription factors, nuclear factor erythroid 2-related factor (Nrf) 1, 2 and 3 were quantified after the above treatments. Generation of reactive oxygen species (ROS) was measured by CM-H2-DCFDA and oxidative-DNA damage was determined by measuring 8-hydroxy-2-deoxyguanosine (8-OHdG). HPIMBD and TIMBD scavenged cellular ROS production, attenuated oxidative DNA damage, increased mRNA and protein expression levels of SOD3 and NQO1 and activated Nrf signaling pathway. Our studies demonstrate that HPIMBD and TIMBD have the potential as novel antioxidants to prevent development of breast cancer.
引用
收藏
页数:9
相关论文
共 50 条
[1]  
[Anonymous], 1987, IARC Monographs, V7, P1
[2]   Nano- and micro-encapsulated systems for enhancing the delivery of resveratrol [J].
Augustin, Mary Ann ;
Sanguansri, Luz ;
Lockett, Trevor .
RESVERATROL AND HEALTH, 2013, 1290 :107-112
[3]   Quantitative analysis of total mitochondrial DNA: Competitive polymerase chain reaction versus real-time polymerase chain reaction [J].
Bhat, HK ;
Epelboym, I .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2004, 18 (04) :180-186
[4]  
BHAT HK, 1995, INT J ONCOL, V7, P527
[5]   REGULATION OF THE FORMATION OF THE MAJOR DIETHYLSTILBESTROL DNA ADDUCT AND SOME EVIDENCE OF ITS STRUCTURE [J].
BHAT, HK ;
HAN, XL ;
GLADEK, A ;
LIEHR, JG .
CARCINOGENESIS, 1994, 15 (10) :2137-2142
[6]   Critical role of oxidative stress in estrogen-induced carcinogenesis [J].
Bhat, HK ;
Calaf, G ;
Hei, TK ;
Loya, T ;
Vadgama, JV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3913-3918
[7]  
Bhat HK, 2002, INT J MOL MED, V9, P271
[8]   Role of Nrf1 in antioxidant response element-mediated gene expression and beyond [J].
Biswas, Madhurima ;
Chan, Jefferson Y. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2010, 244 (01) :16-20
[9]   Molecular origin of cancer: Catechol estrogen-3,4-quinones as endogenous tumor initiators [J].
Cavalieri, EL ;
Stack, DE ;
Devanesan, PD ;
Todorovic, R ;
Dwivedy, I ;
Higginbotham, S ;
Johansson, SL ;
Patil, KD ;
Gross, ML ;
Gooden, JK ;
Ramanathan, R ;
Cerny, RL ;
Rogan, EG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (20) :10937-10942
[10]   Catechol quinones of estrogens in the initiation of breast, prostate, and other human cancers - Keynote lecture [J].
Cavalieri, Ercole ;
Rogan, Eleanor .
ESTROGENS AND HUMAN DISEASES, 2006, 1089 :286-301