A renewal project is proposed to continue to develop marine microorganisms as a new source for antitumor-antibiotics. The project continues as a collaboration between marine natural products chemists and microbiologists at the Scripps Institution of Oceanography (UC-San Diego) and the Oncology Drug Discovery Group at the Bristol-Myers Squibb (BMS), Pharmaceutical Research Institute, in Princeton, NJ. The new project period would emphasize the following collaborative activities aimed at the discovery and development of new agents for the treatment of cancer: - The isolation, cultivation and screening of approximately 1,000 diverse marine microorganisms per year, focusing on marine actinomycetes, Gram- positive unicellular bacteria, gliding bacteria (both cytophaga-like forms and myxobacteria), and, in collaboration with an expert mycologist, to study fungi forming specific associations with marine plants and crustaceans. - The isolation of new bioactive agents, mainly antitumor agents, from cultured marine microorganisms, using a variety of targeted drug discovery screens, including inhibition of topoisomerase I, inhibition of microtubule polymerization and depolymerization, an in vitro cell differentiation assay, an epidermal growth factor (EGF) agonist and antagonist assay and in vitro cytotoxicity testing using drug resistant cell lines. These primary screens will be followed by evaluation in several in vivo murine models, developed in response to the specific biochemistries of these targeted screens. - To continue to develop new understanding of the locations and nutrient adaptations of marine microorganisms as a prerequisite to comprehensive evaluation of chemically-rich taxa found in marine environments. - To continue to create a large, cryopreserved marine microorganism collection, composed of diverse taxonomic groups, to serve as a basis for expanded investigation of this developing resource.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA044848-11
Application #
2376809
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Project Start
1987-04-15
Project End
1999-02-28
Budget Start
1997-03-01
Budget End
1998-02-28
Support Year
11
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Zoology
Type
Schools of Earth Sciences/Natur
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Beuzer, Paolo; Axelrod, Joshua; Trzoss, Lynnie et al. (2016) Single dish gradient screening of small molecule localization. Org Biomol Chem 14:8241-5
Cheng, Yuan-Bin; Jensen, Paul R; Fenical, William (2013) Cytotoxic and Antimicrobial Napyradiomycins from Two Marine-Derived, MAR 4 Streptomyces Strains. European J Org Chem 2013:
Lane, Amy L; Nam, Sang-Jip; Fukuda, Takashi et al. (2013) Structures and comparative characterization of biosynthetic gene clusters for cyanosporasides, enediyne-derived natural products from marine actinomycetes. J Am Chem Soc 135:4171-4
Nam, Sang-Jip; Kauffman, Christopher A; Paul, Lauren A et al. (2013) Actinoranone, a cytotoxic meroterpenoid of unprecedented structure from a marine adapted Streptomyces sp. Org Lett 15:5400-3
Park, Eun-Jung; Pezzuto, John M; Jang, Kyoung Hwa et al. (2012) Suppression of nitric oxide synthase by thienodolin in lipopolysaccharide-stimulated RAW 264.7 murine macrophage cells. Nat Prod Commun 7:789-94
Kondratyuk, Tamara P; Park, Eun-Jung; Yu, Rui et al. (2012) Novel marine phenazines as potential cancer chemopreventive and anti-inflammatory agents. Mar Drugs 10:451-64
Xu, Ying; Kersten, Roland D; Nam, Sang-Jip et al. (2012) Bacterial biosynthesis and maturation of the didemnin anti-cancer agents. J Am Chem Soc 134:8625-32
Kaysser, Leonard; Bernhardt, Peter; Nam, Sang-Jip et al. (2012) Merochlorins A-D, cyclic meroterpenoid antibiotics biosynthesized in divergent pathways with vanadium-dependent chloroperoxidases. J Am Chem Soc 134:11988-91
Eustaquio, Alessandra S; Nam, Sang-Jip; Penn, Kevin et al. (2011) The discovery of salinosporamide K from the marine bacterium ""Salinispora pacifica"" by genome mining gives insight into pathway evolution. Chembiochem 12:61-4
Nam, Sang-Jip; Kauffman, Christopher A; Jensen, Paul R et al. (2011) Isolation and Characterization of Actinoramides A-C, Highly Modified Peptides from a Marine Streptomyces sp. Tetrahedron 67:6707-6712

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