This Program Project Grant is focussed on the development of more effective cancer therapies through integrated and yet diversified contributions of various laboratories of the Department of Experimental Therapeutics and Grace Cancer Drug Center (GCDC) at Roswell Park. New compounds and biologicals are obtained within this program or from outside sources. Emphasis is given on 1) development of therapeutic treatments based on differential sensitivity to differentiation factors of different tissues, 2) development of new inhibitors of protein kinase C, 3) evaluation of the therapeutic potential of intervention on folate polyglutamate metabolism, and 4) verification of therapeutic potential of combination treatments including biological response modifiers (BRM) and identification of BRM correlates of antitumor action. In this proposal, additional emphasis is given to opportunities to modify resistance towards therapeutic applications. The antitumor activity of treatment developed as indicated above obtained from RO-1 supported research in the GCDC is evaluated in vitro and in vivo tumor spectrum. The preclinical toxicology and pharmacology of treatments of interest are studies in different animal species prior to clinical trials. The development of new treatment is integrated closely with both basic progress in the biochemical pharmacology of anticancer drugs and fundamental studies on the regulation of cell metabolism carried out with other grant support in the GCDC: interactions among these approaches and sources of support provide an optimal background for the formulation of new ideas and implementation of studies leading to advances in the therapy of cancer. This Program Project is focused on the development of new treatments of cancer. During the current period of support, the main research emphasis has been on the development of new compounds and treatments developed as a part of this program. Other leads originated in GCDC in RPMI research supported by other funds, or were obtained from outside sources. In some cases the emphasis was on investigations of the biochemical and biological basis for the development of new treatment, in some it was concerned with actual treatment evaluation and development. During the five years of support requested herein, these two main approaches are expected to be continued with added emphasis on the problem of drug resistance and ways to overcome.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA013038-18
Application #
3092597
Study Section
Special Emphasis Panel (SRC (V1))
Project Start
1978-01-01
Project End
1995-01-31
Budget Start
1990-02-01
Budget End
1991-01-31
Support Year
18
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Roswell Park Cancer Institute Corp
Department
Type
DUNS #
City
Buffalo
State
NY
Country
United States
Zip Code
14263
Ojima, Iwao; Borella, Christopher P; Wu, Xinyuan et al. (2005) Design, synthesis and structure-activity relationships of novel taxane-based multidrug resistance reversal agents. J Med Chem 48:2218-28
Berleth, E S; Nadadur, S; Henn, A D et al. (1999) Identification, characterization, and cloning of TIP-B1, a novel protein inhibitor of tumor necrosis factor-induced lysis. Cancer Res 59:5497-506
Huang, B G; Bobek, M (1998) Synthesis and in vitro antitumor activity of some amino-deoxy 7-hexofuranosylpyrrolo[2,3-d]pyrimidines. Carbohydr Res 308:319-28
Ojima, I; Bounaud, P Y; Takeuchi, C et al. (1998) New taxanes as highly efficient reversal agents for multidrug resistance in cancer cells. Bioorg Med Chem Lett 8:189-94
Ehrke, M J; Verstovsek, S; Pocchiari, S K et al. (1998) Thymic anti-tumor effectors in mice cured of lymphoma by cyclophosphamide plus TNF-alpha therapy: phenotypic and functional characterization up to 20 months after initial tumor inoculation. Int J Cancer 76:579-86
Yin, M B; Guo, B; Voigt, W et al. (1998) Novel cellular determinants for reversal of multidrug resistance in cells expressing P170-glycoprotein. Biochim Biophys Acta 1401:265-76
Ehrke, M J; Verstovsek, S; Ujhazy, P et al. (1998) Doxorubicin plus tumor necrosis factor alpha combination treatments in EL4-lymphoma-bearing C57BL/6 mice. Cancer Immunol Immunother 45:287-98
Sharma, A; Glaves, D; Porter, C W et al. (1997) Antitumor efficacy of N1,N11-diethylnorspermine on a human bladder tumor xenograft in nude athymic mice. Clin Cancer Res 3:1239-44
Kramer, D L; Fogel-Petrovic, M; Diegelman, P et al. (1997) Effects of novel spermine analogues on cell cycle progression and apoptosis in MALME-3M human melanoma cells. Cancer Res 57:5521-7
Vanhoefer, U; Yin, M B; Harstrick, A et al. (1997) Carbamoylation of glutathione reductase by N,N-bis(2-chloroethyl)-N- nitrosourea associated with inhibition of multidrug resistance protein (MRP) function. Biochem Pharmacol 53:801-9

Showing the most recent 10 out of 135 publications