Anticancer compounds derived from fungal endophytes: their importance and future challenges

被引:365
作者
Kharwar, Ravindra N. [1 ]
Mishra, Ashish [1 ]
Gond, Surendra K. [1 ]
Stierle, Andrea [2 ]
Stierle, Donald [2 ]
机构
[1] Banaras Hindu Univ, Dept Bot, Mycopathol & Microbial Technol Lab, Varanasi 221005, Uttar Pradesh, India
[2] Univ Montana, Skaggs Sch Pharm, Dept Biomed & Pharmaceut Sci, Missoula, MT 59812 USA
基金
美国国家卫生研究院;
关键词
TOPOISOMERASE-I INHIBITORS; PLANT ANTITUMOR AGENTS; SECALONIC ACID D; SECONDARY METABOLITES; CHAETOMIUM-GLOBOSUM; CYTOTOXIC METABOLITES; NOTHAPODYTES-FOETIDA; HYPERICUM-PERFORATUM; CATHARANTHUS-ROSEUS; NATURAL-PRODUCTS;
D O I
10.1039/c1np00008j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This is a review of anticancer agents isolated from endophytic fungi from 1990-2010. Endophytic fungi are defined as fungi that live asymptomatically within the tissues of higher plants. The designation 'anticancer' is based on the assessment of the authors of the paper of the cytotoxicity of each compound against specific cancer cell lines. Many of the compounds reported here were isolated exclusively from endophytes in culture, while other compounds had been previously reported as chemical constituents of higher plants. The uniqueness of the endophytic community of fungi is stressed as a promising source of novel compounds with anticancer activity, or as an alternative source of compounds originally isolated from higher plants. Endophytes represent a dependable source of specific secondary metabolites, and can be manipulated both physicochemically and genetically to increase yields of desired metabolites and to produce novel analogues of active metabolites.
引用
收藏
页码:1208 / 1228
页数:21
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