Impact of Natural Products on Developing New Anti-Cancer Agents

被引:1048
作者
Cragg, Gordon M. [1 ]
Grothaus, Paul G. [1 ]
Newman, David J. [1 ]
机构
[1] NCI, Nat Prod Branch, Dev Therapeut Program, Div Canc Treatment & Diag,Fairview Ctr, Frederick, MD 21702 USA
关键词
DIVERSITY-ORIENTED SYNTHESIS; PROTEIN-STRUCTURE SIMILARITY; SOLID-PHASE SYNTHESIS; HISTONE DEACETYLASE INHIBITORS; ARYL-HYDROCARBON RECEPTOR; UNCULTIVATED BACTERIAL SYMBIONTS; COMPOUND LIBRARY DEVELOPMENT; PHORBOL ESTER PHARMACOPHORE; TYROSINE KINASE INHIBITORS; BIOSYNTHETIC GENE-CLUSTER;
D O I
10.1021/cr900019j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Plants have a long history of use in the treatment of cancer, and above 3,000 plant species have been identified that can be used against cancer. The first plant-derived agents to advance into clinical use was vinca alkaloids vinblastine and vincristine that were isolated from the Madagascar. Plants and sessile marine organisms release toxic substances that suppress the growth of neighboring species. The cell-to-cell signaling mechanism, known as quorum-sensing, exerted by bacteria to control their density of population growth and biofilm formation, involves the excretion of so-called quorum-sensing compounds. The toxic metabolite, rhizoxin,originally isolated from a rhizopus fungus contaminating rice seedlings, has actually been found to be produced by the endo-symbiotic bacterial species. It has significant implications in development of agents with improved pharmacological properties. Waldmann has developed a new concept for the design of combinatorial libraries based on natural products that is called BIOS.
引用
收藏
页码:3012 / 3043
页数:32
相关论文
共 343 条
[1]   The biotechnological potential of piezophiles [J].
Abe, F ;
Horikoshi, K .
TRENDS IN BIOTECHNOLOGY, 2001, 19 (03) :102-108
[2]   Indirubin and indigo are potent aryl hydrocarbon receptor ligands present in human urine [J].
Adachi, J ;
Mori, Y ;
Matsui, S ;
Takigami, H ;
Fujino, J ;
Kitagawa, H ;
Miller, CA ;
Kato, T ;
Saeki, K ;
Matsuda, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (34) :31475-31478
[3]   The development of proteasome inhibitors as anticancer drugs [J].
Adams, J .
CANCER CELL, 2004, 5 (05) :417-421
[4]  
Alley MC, 2004, CANC DRUG DISC DEV, P125
[5]   The gorgeous inside stories of metal [J].
C and EN Washington .
Chem Eng News, 2006, 20 (14-18) :14-18
[6]   Bioreactor studies on the endophytic fungus Entrophospora infrequens for the production of an anticancer alkaloid camptothecin [J].
Amna, T ;
Puri, SC ;
Verma, V ;
Sharma, JP ;
Khajuria, RK ;
Musarrat, J ;
Spiteller, M ;
Qazi, GN .
CANADIAN JOURNAL OF MICROBIOLOGY, 2006, 52 (03) :189-196
[7]  
Andersen RJ, 2005, ANTICANCER AGENTS FROM NATURAL PRODUCTS, P267
[8]  
Arcamone FM, 2005, ANTICANCER AGENTS FROM NATURAL PRODUCTS, P299
[9]   Pyrrolo[2,3-d]pyrimidines containing an extended 5-substituent as potent and selective inhibitors of lck I [J].
Arnold, LD ;
Calderwood, DJ ;
Dixon, RW ;
Johnston, DN ;
Kamens, JS ;
Munschauer, R ;
Rafferty, P ;
Ratnofsky, SE .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (19) :2167-2170
[10]   Allelopathy and exotic plant invasion: From molecules and genes to species interactions [J].
Bais, HP ;
Vepachedu, R ;
Gilroy, S ;
Callaway, RM ;
Vivanco, JM .
SCIENCE, 2003, 301 (5638) :1377-1380