Studies with animal-tumor models have shown that tumor growth is enhanced by nutritional regimens that replenish the malnourished host. However, clinical observations based upon x-rays and physical examination have not detected changes in tumor growth. These methods for detecting tumor growth are insensitive to subtle changes in tumor growth on the molecular level. The purpose of this proposal is to evaluate the effects of preoperative intravenous hyperalimentation (IVH) on tumor growth parameters as measured by cell kinetic analysis. Patients who have a biopsy proven rectal cancer and who require at least seven days of preoperative IVH will be eligible for this study. Rectal cancer has been selected for this study because adequate tissue sampling of the tumor can be easily obtained through a proctoscope. Rectal tumor biopsies will be obtained before IVH is started, during IVH and at the completion of preoperative IVH just before the surgical resection is done. All tumor sampling will be accomplished by the proctoscope to insure uniform conditions for tissue sampling. Tumor tissue and adjacent normal rectal mucosa will be analyzed for growth fraction, percent cells in S-phase and DNA, RNA and protein content as measured by flow cytometry. The initial tumor cell kinetic parameters will be compared with the subsequent kinetics parameters for each tumor.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA034465-03
Application #
3172176
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1983-06-01
Project End
1986-05-31
Budget Start
1985-06-01
Budget End
1986-05-31
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Type
Hospitals
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Grossie Jr, V B; Yick, J; Alpeter, M et al. (1993) Glutamine stability in biological tissues evaluated by fluorometric analysis. Clin Chem 39:1059-63
Grossie Jr, V B; Nishioka, K; Ajani, J A et al. (1992) Substituting ornithine for arginine in total parenteral nutrition eliminates enhanced tumor growth. J Surg Oncol 50:161-7
Nishioka, K; Grossie, V B; Chang, T H et al. (1991) Colorectal ornithine decarboxylase activity in human mucosa and tumors: elevation of enzymatic activity in distal mucosa. J Surg Oncol 47:117-20
Grossie Jr, V B; Ota, D M; Ajani, J A et al. (1991) Amelioration of thrombocytopenia with concomitant ornithine in sarcoma-bearing rats receiving high dose difluoromethylornithine. Invest New Drugs 9:321-6
Ajani, J A; Ota, D M; Grossie Jr, V B et al. (1990) Evaluation of continuous-infusion alpha-difluoromethylornithine therapy for colorectal carcinoma. Cancer Chemother Pharmacol 26:223-6
Ajani, J A; Ota, D M; Grossie Jr, V B et al. (1989) Alterations in polyamine metabolism during continuous intravenous infusion of alpha-difluoromethylornithine showing correlation of thrombocytopenia with alpha-difluoromethylornithine plasma levels. Cancer Res 49:5761-5
Grossie Jr, V B; Nishioka, K; Chang, T H et al. (1989) Differential effects of parenteral nutrition on tumor growth and erythrocyte polyamine levels in the rat. JPEN J Parenter Enteral Nutr 13:590-5
Grossie Jr, V B; Ota, D M; Ajani, J A et al. (1989) Reduction of difluoromethylornithine-induced thrombocytopenia in rats with ornithine while maintaining antitumor activity. Cancer Res 49:4159-62
Grossie Jr, V B; Ota, D M; Ajani, J A et al. (1988) Influence of total parenteral nutrition on tumor growth and polyamine biosynthesis of fibrosarcoma-bearing rats after induced cachexia. JPEN J Parenter Enteral Nutr 12:441-4
Nishioka, K; Grossie Jr, V B; Ajani, J A et al. (1988) Polyamine-directed preferential nutritional repletion of normal tissues in tumor-bearing hosts. Int J Cancer 42:744-7

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