Recent Advances in Ginsenosides as Potential Therapeutics Against Breast Cancer

被引:31
作者
Guo, Yu-Hang [1 ,2 ]
Kuruganti, Revathimadhubala [1 ]
Gao, Ying [1 ]
机构
[1] Middle Tennessee State Univ, Sch Agr, Int Ginseng Inst, Murfreesboro, TN 37132 USA
[2] Guangxi Univ Chinese Med, Fac Int Educ, Nanning 530001, Guangxi, Peoples R China
关键词
Panax ginseng; Panax quinquefolius; Panax notoginseng; Ginsenosides; Breast Cancer; Mechanism; PREDICT SUBCELLULAR-LOCALIZATION; DNA METHYLATION SITES; AMERICAN GINSENG; PANAX-GINSENG; MULTIDRUG-RESISTANCE; CELLULAR NETWORKING; MCF-7; CELLS; COMPOUND K; WEB SERVER; IN-VITRO;
D O I
10.2174/1568026619666191018100848
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The dried root of ginseng (Panax ginseng C. A. Meyer or Panax quinquefolius L.) is a traditional Chinese medicine widely used to manage cancer symptoms and chemotherapy side effects in Asia. The anti-cancer efficacy of ginseng is attributed mainly to the presence of saponins, which are commonly known as ginsenosides. Ginsenosides were first identified as key active ingredients in Panax ginseng and subsequently found in Panax quinquefolius, both of the same genus. To review the recent advances on anti-cancer effects of ginsenosides against breast cancer, we conducted a literature study of scientific articles published from 2010 through 2018 to date by searching the major databases including Pubmed, SciFinder, Science Direct, Springer, Google Scholar, and CNKI. A total of 50 articles authored in either English or Chinese related to the anti-breast cancer activity of ginsenosides have been reviewed, and the in vitro, in vivo, and clinical studies on ginsenosides are summarized. This review focuses on how ginsenosides exert their anti-breast cancer activities through various mechanisms of action such as modulation of cell growth, modulation of the cell cycle, modulation of cell death, inhibition of angiogenesis, inhibition of metastasis, inhibition of multidrug resistance, and cancer immunemodulation. In summary, recent advances in the evaluation of ginsenosides as therapeutic agents against breast cancer support further pre- clinical and clinical studies to treat primary and metastatic breast tumors.
引用
收藏
页码:2334 / 2347
页数:14
相关论文
共 131 条
[1]  
American Cancer Society, 2018, CANC J CLIN
[2]  
[Anonymous], 2008, CHIN J INTEGR MED, V14, P33, DOI [10.1007/s11655-007-9002, 10.1007/s11655-007-9002-6]
[3]  
[Anonymous], J GINSENG RES
[4]   Phytochemistry of wild populations of Panax quinquefolius L. (North American ginseng) [J].
Assinewe, VA ;
Baum, BR ;
Gagnon, D ;
Arnason, JT .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (16) :4549-4553
[5]  
BESSO H, 1982, CHEM PHARM BULL, V30, P2380
[6]  
Chen K., 2016, CONT MED, V22, P1
[7]   Predicting Drugs Side Effects Based on Chemical-Chemical Interactions and Protein-Chemical Interactions [J].
Chen, Lei ;
Huang, Tao ;
Zhang, Jian ;
Zheng, Ming-Yue ;
Feng, Kai-Yan ;
Cai, Yu-Dong ;
Chou, Kuo-Chen .
BIOMED RESEARCH INTERNATIONAL, 2013, 2013
[8]   Pseudo nucleotide composition or PseKNC: an effective formulation for analyzing genomic sequences [J].
Chen, Wei ;
Lin, Hao ;
Chou, Kuo-Chen .
MOLECULAR BIOSYSTEMS, 2015, 11 (10) :2620-2634
[9]   PseKNC: A flexible web server for generating pseudo K-tuple nucleotide composition [J].
Chen, Wei ;
Lei, Tian-Yu ;
Jin, Dian-Chuan ;
Lin, Hao ;
Chou, Kuo-Chen .
ANALYTICAL BIOCHEMISTRY, 2014, 456 :53-60
[10]   Ginsenoside Rg3 inhibits CXCR4 expression and related migrations in a breast cancer cell line [J].
Chen, Xiao-ping ;
Qian, Lin-lin ;
Jiang, Hong ;
Chen, Jiang-hua .
INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, 2011, 16 (05) :519-523