Abstract

Continuation of a very important investigation sharply focused on the isolation, characterization and structural elucidation of new and potentially useful cancer chemotherapeutic drugs from marine animals has been proposed. Approval would allow continued isolation and characterization of novel anticancer substances from confirmed active extracts of marine invertebrates, and marine vertebrates. Maximum effort would be devoted to marine animal species yielding extracts with outstanding confirmed level activity (T/C greater than 150) in the National Cancer Institute's murine P388 lymphocytic leukemia system. As each problem is solved (or placed in a lower priority due to decreasing or lost activity during fractionation guided by bioassay) it would be replaced by another (of high priority) from a current collection of nearly 400 marine animal species giving extracts with a confirmed level of activity. The lower animals represent an exceedingly productive source of new cancer chemotherapeutic drugs and all effort will be directed at making such new substances available to the Division of Cancer Treatment, National Cancer Institute.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA016049-11
Application #
3164333
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Project Start
1978-07-01
Project End
1991-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
11
Fiscal Year
1987
Total Cost
Indirect Cost

  Institution

Name
Arizona State University-Tempe Campus
Department
Type
Schools of Arts and Sciences
DUNS #
188435911
City
Tempe
State
AZ
Country
United States
Zip Code
85287

  Publications

Pettit, George R; Meng, Yanhui; Gearing, R Patrick et al. (2004) Antineoplastic agents. 522. Hernandia peltata (Malaysia) and Hernandia nymphaeifolia (Republic of Maldives). J Nat Prod 67:214-20
Pettit, G R; Numata, A; Cragg, G M et al. (2000) Isolation and structures of schleicherastatins 1-7 and schleicheols 1 and 2 from the teak forest medicinal tree Schleichera oleosa. J Nat Prod 63:72-8
Pettit, G R; McNulty, J; Herald, D L et al. (1997) Antineoplastic agents. 362. Isolation and X-ray crystal structure of dibromophakellstatin from the Indian ocean sponge Phakellia mauritiana. J Nat Prod 60:180-3
McBain, J A; Eastman, A; Simmons, D L et al. (1996) Phorbol ester augments butyrate-induced apoptosis of colon cancer cells. Int J Cancer 67:715-23
Pettit, G R; Singh, S B; Boyd, M R et al. (1995) Antineoplastic agents. 291. Isolation and synthesis of combretastatins A-4, A-5, and A-6(1a) J Med Chem 38:1666-72
Pettit, G R; Freeman, S; Simpson, M J et al. (1995) Antineoplastic agents 320: synthesis of a practical pancratistatin prodrug. Anticancer Drug Des 10:243-50
Pettit, G R; Pettit 3rd, G R; Backhaus, R A et al. (1995) Antineoplastic agents, 294. Variations in the formation of pancratistatin and related isocarbostyrils in Hymenocallis littoralis. J Nat Prod 58:37-43
Pettit, G R; Pettit 3rd, G R; Groszek, G et al. (1995) Antineoplastic agents, 301. An investigation of the Amaryllidaceae genus Hymenocallis. J Nat Prod 58:756-9
Pettit, G R; Xu, J P; Williams, M D et al. (1994) Isolation and structure of cephalostatins 10 and 11. J Nat Prod 57:52-63
Stanwell, C; Gescher, A; Bradshaw, T D et al. (1994) The role of protein kinase C isoenzymes in the growth inhibition caused by bryostatin 1 in human A549 lung and MCF-7 breast carcinoma cells. Int J Cancer 56:585-92

Showing the most recent 10 out of 54 publications