Phytochemicals: cancer chemoprevention and suppression of tumor onset and metastasis

被引:197
|
作者
Shu, Limin [1 ]
Cheung, Ka-Lung [1 ]
Khor, Tin Oo [1 ]
Chen, Chi [2 ]
Kong, Ah-Ng [1 ]
机构
[1] Rutgers State Univ, Ctr Canc Prevent Res, Dept Pharmaceut, Ernest Mario Sch Pharm, Piscataway, NJ 08854 USA
[2] Univ Minnesota, Dept Food Sci & Nutr, Coll Food Agr & Nat Resource Sci, St Paul, MN 55108 USA
基金
美国国家卫生研究院;
关键词
Phytochemicals; Herbs; Cancer chemoprevention; Metastasis; Molecular targets; NF-KAPPA-B; HUMAN PROSTATE-CANCER; EPITHELIAL-MESENCHYMAL TRANSITION; SQUAMOUS-CELL CARCINOMA; MATRIX-METALLOPROTEINASE INHIBITOR; TRANSACTIVATION DOMAIN ACTIVITY; ANTIOXIDANT-RESPONSIVE ELEMENT; APOPTOSIS-INDUCING LIGAND; HEPATOMA SK-HEP-1 CELLS; DNA-BINDING ACTIVITY;
D O I
10.1007/s10555-010-9239-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Carcinogenesis is a multi-step process which could be prevented by phytochemicals. Phytochemicals from dietary plants and other plant sources such as herbs are becoming increasingly important sources of anticancer drugs or compounds for cancer chemoprevention or adjuvant chemotherapy. Phytochemicals can prevent cancer initiation, promotion, and progression by exerting anti-inflammatory and anti-oxidative stress effects which are mediated by integrated Nrf2, NF-kappa B, and AP-1 signaling pathways. In addition, phytochemicals from herbal medicinal plants and/or some dietary plants developed in recent years have been shown to induce apoptosis in cancer cells and inhibition of tumor growth in vivo. In advanced tumors, a series of changes involving critical signaling molecules that would drive tumor cells undergoing epithelial-mesenchymal transition and becoming invasive. In this review, we will discuss the potential molecular targets and signaling pathways that mediate tumor onset and metastasis. In addition, we will shed light on some of the phytochemicals that are capable of targeting these signaling pathways which would make them potentially applicable to cancer chemoprevention, treatment and control of cancer progression.
引用
收藏
页码:483 / 502
页数:20
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