Targeting cancer with sesterterpenoids: the new potential antitumor drugs

被引:26
|
作者
Zhang, Caiguo [1 ]
Liu, Yan [2 ]
机构
[1] Univ Colorado, Sch Med, Dept Biochem & Mol Genet, Aurora, CO 80045 USA
[2] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Photochem & Plant Resources West Ch, Kunming 650201, Peoples R China
基金
中国国家自然科学基金;
关键词
Terpenoids; Sesterterpenoids; Cancer therapy; Structure-activity relationship; SPONGE RHABDASTRELLA-GLOBOSTELLATA; MARINE SPONGE; CYTOTOXIC SESTERTERPENES; BIOACTIVE SESTERTERPENES; MANOALIDE DERIVATIVES; HASLEA-OSTREARIA; NATURAL-PRODUCTS; DNA-POLYMERASES; GENUS FUSARIUM; HYRTIOS-ERECTA;
D O I
10.1007/s11418-015-0911-y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cancer remains a major cause of death in the world to date. A variety of anticancer drugs have been used in clinical chemotherapy, acting on the particular oncogenic abnormalities that are responsible for malignant transformation and progression. Interestingly, some of these anticancer drugs are developed from natural sources such as plants, marine organisms, and microorganisms. Over the past decades, a family of naturally occuring molecules, namely sesterterpenoids, has been isolated from different organisms and they exhibit significant potential in the inhibition of tumor cells in vitro, while the molecular targets of these compounds and their functional mechanisms are still obscure. In this review, we summarize and discuss the functions of these sesterterpenoids in the inhibition of cancer cells. Moreover, we also highlight and discuss chemical structure-activity relationships of some compounds, demonstrating their pervasiveness and importance in cancer therapy.
引用
收藏
页码:255 / 266
页数:12
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