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. 1980 Mar;191(3):316–322. doi: 10.1097/00000658-198003000-00010

Tumor growth in experimental animals: nutritional manipulation and chemotherapeutic response in the rat.

J M Daly, H M Reynolds, B J Rowlands, S J Dudrick, E M Copeland 3rd
PMCID: PMC1344702  PMID: 7362297

Abstract

The effects of nutritional manipulation on host body weight dynamics, tumor growth patterns and host-tumor responses to chemotherapy were studied in Sprague-Dawley rats with Walker-256 carcinosarcomas. Group I maintained throughout on a regular diet (RD) gained carcass weight steadily. Group II lost carcass weight while fed a protein-free diet (PFD) but rapidly gained weight after switching to RD on day 15. Mean tumor volume increased 105% in Group I from day 15 to 21, 218% in Group II and 77% in Group III (continued on PFD p less than 0.05). From day 21 to day 33 tumor growth patterns were similar in Groups I and II, while mean tumor volume eventually plateaued in Group III. In Study B, Group II animals were given Methotrexate (MTX-20 mg/kg) two days and six days after switching from PFD to RD. The mean change in tumor volume in the MTX-treated rats was 1.31 +/- 0.1 cm3 compared with 8.14 +/- 0.1 cm3 (p less than 0.001) in the saline-treated control rats. MTX did not significantly affect tumor growth patterns in Group III (PFD) rats. In Study A, protein-calorie malnutrition resulted in host carcass weight loss and tumor growth retardation while nutritional repletion restored host carcass weight and stimulated tumor growth. In Study B, MTX was maximally effective in tumor-bearing rats that were switched from PFD to RD demonstrating that nutritional manipulation can improve host nutritional status and increase tumor response to chemotherapy.

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Selected References

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  1. Cameron I. L., Ackley W. J., Rogers W. Responses of hepatoma-bearing rats to total parenteral hyperalimentation and to ad libitum feeding. J Surg Res. 1977 Sep;23(3):189–195. doi: 10.1016/0022-4804(77)90020-8. [DOI] [PubMed] [Google Scholar]
  2. Cameron I. L., Pavlat W. A. Stimulation of growth of a transplantable hepatoma in rats by parenteral nutrition. J Natl Cancer Inst. 1976 Mar;56(3):597–602. doi: 10.1093/jnci/56.3.597. [DOI] [PubMed] [Google Scholar]
  3. Cameron I. L., Rogers W. Total intravenous hyperalimentation and hydroxyurea chemotherapy in hepatoma-bearing rats. J Surg Res. 1977 Oct;23(4):279–288. doi: 10.1016/0022-4804(77)90177-9. [DOI] [PubMed] [Google Scholar]
  4. Copeland E. M., Macfayden B. V., Jr, Dudrick S. J. Intravenous hyperalimentation in cancer patients. J Surg Res. 1974 Mar;16(3):241–247. doi: 10.1016/0022-4804(74)90038-9. [DOI] [PubMed] [Google Scholar]
  5. DEVIK F., ELSON L. A., KOLLER P. C., LAMERTON L. F. The influence of diet on the Walker rat carcinoma 256, and its response to x-radiation; cytological and histological investigations. Br J Cancer. 1950 Sep;4(3):298–314. doi: 10.1038/bjc.1950.28. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Daly J. M., Copeland E. M., Dudrick S. J. Effects of intravenous nutrition on tumor growth and host immunocompetence in malnourished animals. Surgery. 1978 Nov;84(5):655–658. [PubMed] [Google Scholar]
  7. Hill B. T., Baserga R. The cell cycle and its significance for cancer treatment. Cancer Treat Rev. 1975 Sep;2(3):159–175. doi: 10.1016/s0305-7372(75)80001-6. [DOI] [PubMed] [Google Scholar]
  8. Meyer J. A. Potentiation of solid-tumor chemotherapy by metabolic alteration. Ann Surg. 1974 Jan;179(1):88–93. doi: 10.1097/00000658-197401000-00017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Morrison S. D. Limited capacity for motor activity as a cause for declining food intake in cancer. J Natl Cancer Inst. 1973 Nov;51(5):1535–1539. doi: 10.1093/jnci/51.5.1535. [DOI] [PubMed] [Google Scholar]
  10. Oram-Smith J. C., Stein T. P., Wallace H. W., Mullen J. L. Intravenous nutrition and tumor host protein metabolism. J Surg Res. 1977 May;22(5):499–503. doi: 10.1016/0022-4804(77)90032-4. [DOI] [PubMed] [Google Scholar]
  11. Ota D. M., Copeland E. M., 3rd, Strobel H. W., Jr, Daly J., Gum E. T., Guinn E., Dudrick S. J. The effect of protein nutrition on host and tumor metabolism. J Surg Res. 1977 Mar;22(3):181–188. doi: 10.1016/0022-4804(77)90132-9. [DOI] [PubMed] [Google Scholar]
  12. Reilly J. J., Goodgame J. T., Jones D. C., Brennan M. F. DNA synthesis in rat sarcoma and liver: the effect of starvation. J Surg Res. 1977 Mar;22(3):281–286. doi: 10.1016/0022-4804(77)90144-5. [DOI] [PubMed] [Google Scholar]
  13. Souchon E. A., Copeland E. M., Watson P., Dudrick S. J. Intravenous hyperalimentation as an adjunct to cancer chemotherapy with 5-fluorouracil. J Surg Res. 1975 Apr;18(4):451–454. doi: 10.1016/0022-4804(75)90108-0. [DOI] [PubMed] [Google Scholar]
  14. Steiger E., Oram-Smith J., Miller E., Kuo L., Vars H. M. Effects of nutrition on tumor growth and tolerance to chemotherapy. J Surg Res. 1975 Apr;18(4):455–466. doi: 10.1016/0022-4804(75)90109-2. [DOI] [PubMed] [Google Scholar]
  15. TANNENBAUM A., SILVERSTONE H. Nutrition in relation to cancer. Adv Cancer Res. 1953;1:451–501. doi: 10.1016/s0065-230x(08)60009-3. [DOI] [PubMed] [Google Scholar]
  16. TEREPKA A. R., WATERHOUSE C. Metabolic observations during the forced feeding of patients with cancer. Am J Med. 1956 Feb;20(2):225–238. doi: 10.1016/0002-9343(56)90193-0. [DOI] [PubMed] [Google Scholar]

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