Beet root juice protects against doxorubicin toxicity in cardiomyocytes while enhancing apoptosis in breast cancer cells

被引:24
作者
Das, Sayantanee [1 ,4 ]
Filippone, Scott M. [1 ]
Williams, Denise S. [2 ]
Das, Anindita [1 ]
Kukreja, Rakesh C. [1 ,3 ]
机构
[1] Virginia Commonwealth Univ, Pauley Heart Ctr, Div Cardiol, Dept Internal Med, Richmond, VA 23298 USA
[2] Mills Edwin Godwin High Sch, Ctr Sci Math & Technol, Richmond, VA 23238 USA
[3] Virginia Commonwealth Univ, Pauley Heart Ctr, Div Cardiol, 1101 East Marshall St,Room 7020D, Richmond, VA 23298 USA
[4] Duke Univ, Durham, NC 27708 USA
基金
美国国家卫生研究院;
关键词
Apoptosis; Beet root juice; Breast cancer cells; Cardiomyocytes; Doxorubicin; Reactive oxygen species; BETA-VULGARIS L; ISCHEMIA-REPERFUSION INJURY; CARDIAC-MUSCLE-CELLS; GROWTH-FACTOR I; POLY(ADP-RIBOSE) POLYMERASE; INDUCED CARDIOTOXICITY; OXIDATIVE STRESS; PHOSPHODIESTERASE-5; INHIBITOR; INDUCED CARDIOMYOPATHY; MEDIATED APOPTOSIS;
D O I
10.1007/s11010-016-2789-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Doxorubicin (DOX, Adriamycin) is a broad-spectrum chemotherapeutic drug used to treat a variety of cancers, although its clinical use is restricted by irreversible cardiotoxicity. Earlier studies show that beet root juice (BRJ), a natural and safe herbal product with high levels of nitrate and antioxidants, is a potent chemopreventive agent; however, its cardioprotective function is yet to be established. The goal of this study was to determine the protective effect of BRJ against DOX-induced cardiotoxicity, and its effect on DOX-induced cytotoxicity in MDA-MB-231 breast cancer cells. Adult rat cardiomyocytes and MDA-MB-231 cells were exposed to different concentrations of BRJ (0.5, 5, 50, 250, and 500 A mu g/ml) with or without DOX. Cell death, measured by trypan blue staining, was significantly reduced in cardiomyocytes but increased in MDA-MB-231 following 24 h of co-treatment with BRJ and DOX. Cell viability was also significantly reduced after BRJ and DOX co-treatment in MDA-MB-231 cells. Similarly, DOX-induced apoptosis, as determined by TUNEL assay, was significantly reduced following treatment with BRJ for 48 h in cardiomyocytes. In contrast, BRJ significantly increased DOX-mediated apoptosis in cancer cells with activation of poly(ADP-ribose) polymerase (PARP) and increased the Bax:Bcl-2 ratio. DOX-induced generation of reactive oxygen species (ROS) was reduced following co-treatment with BRJ in cardiomyocytes but increased dose-dependently with BRJ in MDA-MB-231 cells. In conclusion, lower concentrations of BRJ with DOX represented the most effective combination of cardioprotection and chemoprevention. These findings provide insight into the possible cardioprotective ability of BRJ in cancer patients treated with anthracycline chemotherapeutic drugs.
引用
收藏
页码:89 / 101
页数:13
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