Marine pharmacology in 2001-2: antitumour and cytotoxic compounds

被引:92
作者
Mayer, AMS
Gustafson, KR
机构
[1] Midwestern Univ, Chicago Coll Osteopath Med, Dept Pharmacol, Downers Grove, IL 60515 USA
[2] NCI, Ctr Canc Res, Mol Targets Dev Program, Frederick, MD 21702 USA
关键词
marine; antitumour; cytotoxicity; anticancer; antineoplastic; agents; preclinical; clinical; pharmacology; review;
D O I
10.1016/j.ejca.2004.09.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
During 2001 and 2002, marine antitumour pharmacology research aimed at the discovery of novel antitumour agents was published in 175 peer-reviewed articles. The purpose of this paper is to present a structured Review of the antitumour and cytotoxic properties of 97 marine natural products, many of them novel compounds that belong to diverse structural classes, including polyketides, terpenes, steroids, and peptides. The organisms yielding these bioactive compounds comprise a taxonomically diverse group of marine invertebrate animals, algae, fungi and bacteria. Antitumour pharmacological studies were conducted with 30 structurally characterised natural marine products in a number of experimental and clinical models which further defined their mechanisms of action. Particularly potent in vitro cytotoxicity data generated with murine and human turnout cell lines was reported for 67 novel marine chemicals with as yet undetermined mechanisms of action. Noteworthy, is the fact that marine anticancer research was sustained by a collaborative effort, involving researchers from Australia, Brazil, Canada, Denmark, Egypt, France, Germany, Italy, Japan, Netherlands, New Zealand, the Phillipines, Russia, Singapore, South Korea, Thailand, Taiwan, Turkey, Spain, Switzerland, Taiwan, Thailand, Turkey, and the United States. Finally, this 2001-2 overview of the marine pharmacology literature highlights the fact that the discovery of novel marine antitumour agents has continued at the same pace as during 1998, 1999 and 2000. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2676 / 2704
页数:29
相关论文
共 176 条
[21]   Effects of marine sponge extracts on mitogen-activated protein kinase (MAPK/ERK1,2) activity in SW-13 human adrenal carcinoma cells [J].
Brown, JW ;
Kesler, CT ;
Neary, JT ;
Fishman, LM .
TOXICON, 2001, 39 (12) :1835-1839
[22]   Junceol A, a new sesquiterpenoid from the sea pen Virgularia juncea [J].
Chen, SP ;
Sung, PJ ;
Duh, CY ;
Dai, CF ;
Sheu, JH .
JOURNAL OF NATURAL PRODUCTS, 2001, 64 (09) :1241-1242
[23]   Reversal of drug resistance mediated by multidrug resistance protein (MRP) 1 by dual effects of agosterol A on MRP1 function [J].
Chen, ZS ;
Aoki, S ;
Komatsu, M ;
Ueda, K ;
Sumizawa, T ;
Furukawa, T ;
Okumura, H ;
Ren, XQ ;
Belinsky, MG ;
Lee, K ;
Kruh, GD ;
Kobayashi, M ;
Akiyama, S .
INTERNATIONAL JOURNAL OF CANCER, 2001, 93 (01) :107-113
[24]   Bryostatin/ionomycin-activated T cells mediate regression of established tumors [J].
Chin, CS ;
Graham, LJ ;
Hamad, GG ;
George, KR ;
Bear, HD .
JOURNAL OF SURGICAL RESEARCH, 2001, 98 (02) :108-115
[25]   Induction of apoptosis and CD10/neutral endopeptidase expression by jaspamide in HL-60 line cells [J].
Cioca, DP ;
Kitano, K .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (08) :1377-1387
[26]  
Cragg LH, 2002, CLIN CANCER RES, V8, P2123
[27]   Novel sesterterpenoid and norsesterterpenoid RCE-protease inhibitors isolated from the marine sponge Hippospongia sp. [J].
Craig, KS ;
Williams, DE ;
Hollander, I ;
Frommer, E ;
Mallon, R ;
Collins, K ;
Wojciechowicz, D ;
Tahir, A ;
Van Soest, R ;
Andersen, RJ .
TETRAHEDRON LETTERS, 2002, 43 (27) :4801-4804
[28]   Bryostatin-1 and IL-2 synergize to induce IFN-γ expression in human peripheral blood T cells:: Implications for cancer immunotherapy [J].
Curiel, RE ;
Garcia, CS ;
Farooq, L ;
Aguero, MF ;
Espinoza-Delgado, I .
JOURNAL OF IMMUNOLOGY, 2001, 167 (09) :4828-4837
[29]   Editorial comment on "In vitro toxicity of ET-743 and Aplidine, two marine-derived antineoplastics, on human bone marrow haematopoietic progenitors:: comparison with the clinical results" by Albella and colleagues [J].
D'Incalci, M .
EUROPEAN JOURNAL OF CANCER, 2002, 38 (10) :1297-1297
[30]   Unique pattern of ET-743 activity in different cellular systems with defined deficiencies in DNA-repair pathways [J].
Damia, G ;
Silvestri, S ;
Carrassa, L ;
Filiberti, L ;
Faircloth, GT ;
Liberi, G ;
Foiani, M ;
D'Incalci, M .
INTERNATIONAL JOURNAL OF CANCER, 2001, 92 (04) :583-588