Hitting the Golden TORget: Curcumin's Effects on mTOR Signaling

被引:37
作者
Beevers, Christopher S. [1 ]
Zhou, Hongyu [2 ]
Huang, Shile [3 ,4 ]
机构
[1] Ross Univ, Dept Pharmacol, Sch Med, Picard, Portsmouth, Dominica
[2] Chinese Acad Sci, Kunming Inst Bot, Kunming 650201, Yunnan Province, Peoples R China
[3] Louisiana State Univ, Hlth Sci Ctr, Dept Biochem & Mol Biol, Shreveport, LA 71105 USA
[4] Louisiana State Univ, Hlth Sci Ctr, Feist Weiller Canc Ctr, Shreveport, LA 71105 USA
关键词
Curcumin; mTOR; Akt; Cancer; Cell proliferation; Cell death; I CLINICAL-TRIAL; P70; S6; KINASE; MAMMALIAN TARGET; AMINO-ACID; TRANSLATION INITIATION; CELL-PROLIFERATION; AKT ACTIVATION; RAPAMYCIN; PHOSPHORYLATION; PROTEIN;
D O I
10.2174/1871520611313070004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The polyphenol natural product curcumin possesses a plethora of biological and pharmacological properties. For years, much interest has been placed in the development and use of curcumin and its derivatives for the prevention and treatment of cardiovascular, diabetic, and neurodegenerative diseases, as well as cancer. Increasing evidence suggests that curcumin displays amazing molecular versatility, and the number of its proposed cellular targets grows as the research continues. The mammalian target of rapamycin ( mTOR) is a master kinase, regulating cell growth/proliferation, survival, and motility. Dysregulated mTOR signaling occurs frequently in cancer, and targeting mTOR signaling is a promising strategy for cancer therapy. Recent studies have identified mTOR as a novel target of curcumin. Here we focus on reviewing current knowledge regarding the effects of curcumin on mTOR signaling for better understanding the anticancer mechanism of curcumin. The emerging studies of mTOR signaling and clinical studies on curcumin with cancer patients are also discussed here.
引用
收藏
页码:988 / 994
页数:7
相关论文
共 100 条
[1]  
Aggarwal BB, 2003, ANTICANCER RES, V23, P363
[2]   Bioavailability of curcumin: Problems and promises [J].
Anand, Preetha ;
Kunnumakkara, Ajaikumar B. ;
Newman, Robert A. ;
Aggarwal, Bharat B. .
MOLECULAR PHARMACEUTICS, 2007, 4 (06) :807-818
[3]   Evidence that curcumin suppresses the growth of malignant gliomas in vitro and in vivo through induction of autophagy: Role of Akt and extracellular signal-regulated kinase signaling pathways [J].
Aoki, Hiroshi ;
Takada, Yasunari ;
Kondo, Seiji ;
Sawaya, Raymond ;
Aggarwal, Bharat B. ;
Kondo, Yasuko .
MOLECULAR PHARMACOLOGY, 2007, 72 (01) :29-39
[4]   Curcumin: An Anti-Inflammatory Molecule from a Curry Spice on the Path to Cancer Treatment [J].
Basnet, Purusotam ;
Skalko-Basnet, Natasa .
MOLECULES, 2011, 16 (06) :4567-4598
[5]  
Beevers C.S., 2011, Botanics: Targets and Therapy, V1, P5, DOI DOI 10.2147/BTAT.S17244
[6]   Curcumin inhibits the mammalian target of rapamycin-mediated signaling pathways in cancer cells [J].
Beevers, Christopher S. ;
Li, Fengjun ;
Liu, Lei ;
Huang, Shile .
INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (04) :757-764
[7]   Curcumin Disrupts the Mammalian Target of Rapamycin-Raptor Complex [J].
Beevers, Christopher S. ;
Chen, Long ;
Liu, Lei ;
Luo, Yan ;
Webster, Nicholas J. G. ;
Huang, Shile .
CANCER RESEARCH, 2009, 69 (03) :1000-1008
[8]   SHIP inhibits Akt activation in B cells through regulation of Akt membrane localization [J].
Carver, DJ ;
Aman, MJ ;
Ravichandran, KS .
BLOOD, 2000, 96 (04) :1449-1456
[9]   Rapamycin and other longevity-promoting compounds enhance the generation of mouse induced pluripotent stem cells [J].
Chen, Taotao ;
Shen, Li ;
Yu, Jie ;
Wan, Hongjiang ;
Guo, Ao ;
Chen, Jiekai ;
Long, Yuan ;
Zhao, Jian ;
Pei, Gang .
AGING CELL, 2011, 10 (05) :908-911
[10]  
Cheng AL, 2001, ANTICANCER RES, V21, P2895