β-lonone and its analogs as promising anticancer agents

被引:82
作者
Ansari, Mahsa [1 ]
Emami, Saeed [2 ,3 ]
机构
[1] Mazandaran Univ Med Sci, Fac Pharm, Pharmaceut Sci Res Ctr, Student Res Comm, Sari, Iran
[2] Mazandaran Univ Med Sci, Fac Pharm, Dept Med Chem, Sari, Iran
[3] Mazandaran Univ Med Sci, Fac Pharm, Pharmaceut Sci Res Ctr, Sari, Iran
关键词
beta-lonone; Terpenoid derivatives; Anticancer agents; Anti-proliferative activity; Apoptosis; Drug design; NF-KAPPA-B; IONONE DERIVED CHALCONES; CHROMENE-BASED CHALCONES; CARCINOMA CANCER-CELLS; IN-VITRO CYTOTOXICITY; BIOLOGICAL EVALUATION; PROSTATE-CANCER; MAMMARY CARCINOGENESIS; PRENEOPLASTIC LESIONS; HISTONE DEACETYLASE;
D O I
10.1016/j.ejmech.2016.07.037
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
beta-lonone is an end-ring analog of beta-carotenoids which widely distributed in fruit and vegetables. Recent studies have demonstrated anti-proliferative, anti-metastatic and apoptosis induction properties of beta-ionone in vitro and in vivo. Also, the studies have focused on investigating the beta-ionone action on different types of malignant cells and the possible mechanisms of action. Moreover, the quest of new synthetic beta-ionone-based compounds possessing anti-proliferative, anti-metastatic and apoptosis induction activities may enable the discovery of compounds which can be used in combination regimes thus overcoming tumor resistance to conventional anticancer agents. These new agents will also be useful for targeting distinct signaling pathways, to activate selectively mechanisms for apoptosis in cancer cells but devoid of undesirable side effects. In this paper, we reviewed the potentialities of beta-ionone and related compounds in cancer prevention and chemotherapy. (C) 2016 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:141 / 154
页数:14
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