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lüll Mechanism targeted discovery of antitumor marine natural products Nagle DG; Zhou YD; Mora FD; Mohammed KA; Kim YPCurr Med Chem 2004[Jul]; 11 (13): 1725-56Antitumor drug discovery programs aim to identify chemical entities for use in the treatment of cancer. Many strategies have been used to achieve this objective. Natural products have always played a major role in anticancer medicine and the unique metabolites produced by marine organisms have increasingly become major players in antitumor drug discovery. Rapid advances have occurred in the understanding of tumor biology and molecular medicine. New insights into mechanisms responsible for neoplastic disease are significantly changing the general philosophical approach towards cancer treatment. Recently identified molecular targets have created exciting new means for disrupting tumor-specific cell signaling, cell division, energy metabolism, gene expression, drug resistance and blood supply. Such tumor-specific treatments could someday decrease our reliance on traditional cytotoxicity-based chemotherapy and provide new less toxic treatment options with significantly fewer side effects. Novel molecular targets and state-of-the-art, molecular mechanism-based screening methods have revitalized antitumor research and these changes are becoming an ever-increasing component of modern antitumor marine natural products research. This review describes marine natural products identified using tumor-specific mechanism-based assays for regulators of angiogenesis, apoptosis, cell cycle, macromolecule synthesis, mitochondrial respiration, mitosis, multidrug efflux and signal transduction. Special emphasis is placed on natural products directly discovered using molecular mechanism-based screening.|*Seawater[MESH]|Angiogenesis Inhibitors/chemistry/isolation & purification/pharmacology[MESH]|Animals[MESH]|Antineoplastic Agents/*chemistry/isolation & purification/pharmacology[MESH]|Biological Products/*chemistry/isolation & purification/pharmacology[MESH]|Drug Industry[MESH]|Drug Resistance, Multiple[MESH]|Humans[MESH]|Mitochondria/drug effects[MESH]|Neoplasms/drug therapy[MESH]|Signal Transduction[MESH] |