Induction of Cancer Cell Death by Isoflavone: The Role of Multiple Signaling Pathways

被引:53
作者
Li, Yiwei [1 ]
Kong, Dejuan [1 ]
Bao, Bin [1 ]
Ahmad, Aamir [1 ]
Sarkar, Fazlul H. [1 ]
机构
[1] Wayne State Univ, Sch Med, Hudson Webber Canc Res Ctr 740, Barbara Ann Karmanos Canc Inst,Dept Pathol, Detroit, MI 48201 USA
关键词
cell signaling; apoptosis; isoflavone; NF-KAPPA-B; PROSTATE-SPECIFIC ANTIGEN; MAMMARY EPITHELIAL-CELLS; CDNA MICROARRAY ANALYSIS; ANDROGEN RECEPTOR; BREAST-CANCER; DOWN-REGULATION; SOY ISOFLAVONE; UP-REGULATION; LUNG-CANCER;
D O I
10.3390/nu3100877
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Soy isoflavones have been documented as dietary nutrients broadly classified as "natural agents" which plays important roles in reducing the incidence of hormone-related cancers in Asian countries, and have shown inhibitory effects on cancer development and progression in vitro and in vivo, suggesting the cancer preventive or therapeutic activity of soy isoflavones against cancers. Emerging experimental evidence shows that isoflavones could induce cancer cell death by regulating multiple cellular signaling pathways including Akt, NF-kappa B, MAPK, Wnt, androgen receptor (AR), p53 and Notch signaling, all of which have been found to be deregulated in cancer cells. Therefore, homeostatic regulation of these important cellular signaling pathways by isoflavones could be useful for the activation of cell death signaling, which could result in the induction of apoptosis of both pre-cancerous and/or cancerous cells without affecting normal cells. In this article, we have attempted to summarize the current state-of-our-knowledge regarding the induction of cancer cell death pathways by isoflavones, which is believed to be mediated through the regulation of multiple cellular signaling pathways. The knowledge gained from this article will provide a comprehensive view on the molecular mechanism(s) by which soy isoflavones may exert their effects on the prevention of tumor progression and/or treatment of human malignancies, which would also aid in stimulating further in-depth mechanistic research and foster the initiation of novel clinical trials.
引用
收藏
页码:877 / 896
页数:20
相关论文
共 128 条
[1]   Soy Isoflavones in Conjunction With Radiation Therapy in Patients With Prostate Cancer [J].
Ahmad, Iftekhar U. ;
Forman, Jeffrey D. ;
Sarkar, Fazlul H. ;
Hillman, Gilda G. ;
Heath, Elisabeth ;
Vaishampayan, Ulka ;
Cher, Michael L. ;
Andic, Fundagul ;
Rossi, Peter J. ;
Kucuk, Omer .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2010, 62 (07) :996-1000
[2]   Mechanism of activation of protein kinase B by insulin and IGF-1 [J].
Alessi, DR ;
Andjelkovic, M ;
Caudwell, B ;
Cron, P ;
Morrice, N ;
Cohen, P ;
Hemmings, BA .
EMBO JOURNAL, 1996, 15 (23) :6541-6551
[3]  
Alhasan SA, 2001, CLIN CANCER RES, V7, P4174
[4]   Wnt proteins prevent apoptosis of both uncommitted osteoblast progenitors and differentiated osteoblasts by β-catenin-dependent and -independent signaling cascades involving Src/ERK and phosphatidylinositol 3-kinase/AKT [J].
Almeida, M ;
Han, L ;
Bellido, T ;
Manolagas, SC ;
Kousteni, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (50) :41342-41351
[5]   Proximal events in Wnt signal transduction [J].
Angers, Stephane ;
Moon, Randall T. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (07) :468-477
[6]   Inhibition of NF-κB sensitizes human pancreatic carcinoma cells to apoptosis induced by etoposide (VP16) or doxorubicin [J].
Arlt, A ;
Vorndamm, J ;
Breitenbroich, M ;
Fölsch, UR ;
Kalthoff, H ;
Schmidt, WE ;
Schäfer, H .
ONCOGENE, 2001, 20 (07) :859-868
[7]   Mining the Wnt pathway for cancer therapeutics [J].
Barker, Nick ;
Clevers, Hans .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (12) :997-1014
[8]   Genistein reduces NF-κB in T lymphoma cells via a caspase-mediated cleavage of IκBα [J].
Baxa, DM ;
Yoshimura, FK .
BIOCHEMICAL PHARMACOLOGY, 2003, 66 (06) :1009-1018
[9]  
Behrens J, 2000, ANN NY ACAD SCI, V910, P21
[10]   Role of poly(ADP-ribose) polymerase (PARP) cleavage in apoptosis - Caspase 3-resistant PARP mutant increases rates of apoptosis in transfected cells [J].
Boulares, AH ;
Yakovlev, AG ;
Ivanova, V ;
Stoica, BA ;
Wang, GP ;
Iyer, S ;
Smulson, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (33) :22932-22940