The overall aim of this research is to obtain new marine natural products with bioactivity against solid tumors, especially colon, breast, prostate, and lung cancers. These are the tumors that are resistant to most of the known anticancer drugs and are responsible for 67 percent of the annual cancer deaths in the US. The work will be carried out through a collaboration between the University of California, Santa Cruz (UCSC) Marine Natural Products team and the Experimental Therapeutics Investigators, moving in January 1999 from Wayne Sate University (WSU) Cancer Center to the Henry Ford Cancer Center (HFCC) (Detroit).
The specific aims of this grant are: (a) To use bioassay-guided isolations in the discovery of new marine natural product anticancer candidates. (b) To employ an in vitro mammalian cell assay in order to focus on agents with """"""""cellular selectivity"""""""" for solid tumors. (c) To investigate under-explored sponge taxonomic orders such as the Choristida, Dendroceratida, Hadromerida, Haplosclerida, Lithistida, Poeciloslcerida, and Spirophorida. (d) To develop a library of marine sponge-derived fungal cultures whose saltwater fermentation products will be explored for their potential to act as selective cytotoxic agents. (e) To continue work on leads obtained from prior research involving potent tumor selective alkaloids and oxygen heterocycles which include: sponge compounds-cyclocinamide A (6), ethyldidehydroplakortide Z (22), milnamide B (31), reticulatine A (41c), methylnuapapuanoate A (44), and a sponge-fungal derived metabolite-tenuazonic acid (50). (f) To continue, but on a limited basis, the study of sponge taxa (especially Theonella and Stellata) which might have a broadened scope of natural products owing to the presence of symbionts. (g) To complete the structure elucidation of active compounds. (h) To preliminarily develop new anticancer leads for future clinical trials by using in vivo evaluation in mouse models to examine the in vitro active compounds. Lead compounds will be identified by a multistaged process. Indo-Pacific sponges will be explored. The leads (above) from past research will be examined by scale-up isolation to complete in vivo studies and analogs will also be sought from other extracts. There are 32 extracts on hand which are solid tumor selective that will be pursued to isolate their active constituents. Annual expeditions will generate more than 100 new organisms for study which should provide five to ten new compounds for investigation. Sponge-derived fungi will be grown in saltwater culture and those with solid tumor selective extracts will be candidates for isolation work. An adjunct to the HFCC in vitro mammalian cell assays will be """"""""bench-top assays"""""""" carried out at UCSC.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA047135-13
Application #
6375798
Study Section
Special Emphasis Panel (ZRG1-MCHA (01))
Project Start
1989-04-01
Project End
2003-04-30
Budget Start
2001-05-01
Budget End
2002-04-30
Support Year
13
Fiscal Year
2001
Total Cost
$343,035
Indirect Cost
Name
University of California Santa Cruz
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
City
Santa Cruz
State
CA
Country
United States
Zip Code
95064
Lorig-Roach, Nicholas; Hamkins-Indik, Frances; Johnson, Tyler A et al. (2018) The potential of achiral sponge-derived and synthetic bromoindoles as selective cytotoxins against PANC-1 tumor cells. Tetrahedron 74:217-223
Cooper, Jason K; Li, Kelin; Aubé, Jeffrey et al. (2018) Application of the DP4 Probability Method to Flexible Cyclic Peptides with Multiple Independent Stereocenters: The True Structure of Cyclocinamide A. Org Lett 20:4314-4317
Lorig-Roach, Nicholas; Still, Patrick C; Coppage, David et al. (2017) Evaluating Nitrogen-Containing Biosynthetic Products Produced by Saltwater Culturing of Several California Littoral Zone Gram-Negative Bacteria. J Nat Prod 80:2304-2310
Fraley, Amy E; Garcia-Borràs, Marc; Tripathi, Ashootosh et al. (2017) Function and Structure of MalA/MalA', Iterative Halogenases for Late-Stage C-H Functionalization of Indole Alkaloids. J Am Chem Soc 139:12060-12068
Sabry, Omar M M; Goeger, Douglas E; Valeriote, Frederick A et al. (2017) Cytotoxic halogenated monoterpenes from Plocamium cartilagineum. Nat Prod Res 31:261-267
Zhang, Huawei; Dong, Menglian; Chen, Jianwei et al. (2017) Bioactive Secondary Metabolites from the Marine Sponge Genus Agelas. Mar Drugs 15:
Zhang, Huawei; Crews, Phillip; Tenney, Karen et al. (2017) Cytotoxic Phyllactone Analogs from the Marine Sponge Phyllospongia papyrecea. Med Chem 13:295-300
Lin, Sheng; McCauley, Erin P; Lorig-Roach, Nicholas et al. (2017) Another Look at Pyrroloiminoquinone Alkaloids-Perspectives on Their Therapeutic Potential from Known Structures and Semisynthetic Analogues. Mar Drugs 15:
Johnson, Tyler A; Milan-Lobo, Laura; Che, Tao et al. (2017) Identification of the First Marine-Derived Opioid Receptor ""Balanced"" Agonist with a Signaling Profile That Resembles the Endorphins. ACS Chem Neurosci 8:473-485
Zhang, Huawei; Loveridge, Steven T; Tenney, Karen et al. (2016) A new 3-alkylpyridine alkaloid from the marine sponge Haliclona sp. and its cytotoxic activity. Nat Prod Res 30:1262-5

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