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Tumor growth in experimental animals: nutritional manipulation and chemotherapeutic response in the rat.实验动物中的肿瘤生长:大鼠的营养调控与化疗反应
Ann Surg. 1980 Mar;191(3):316-22. doi: 10.1097/00000658-198003000-00010.
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Effects of nutritional repletion on host and tumor response to chemotherapy.营养补充对宿主及肿瘤化疗反应的影响。
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[Energy metabolism and experimental malignant tumor development].[能量代谢与实验性恶性肿瘤发展]
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Effect of diets with different protein levels on the growth of Walker 256 carcinosarcoma in rats.不同蛋白质水平的饮食对大鼠Walker 256癌肉瘤生长的影响。
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Effect of nutritional status on the hepatobiliary excretion of methotrexate in the rat.营养状况对大鼠甲氨蝶呤肝胆排泄的影响。
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31P NMR study of the impact of dietary manipulation on tumor metabolism and response to methotrexate.饮食调控对肿瘤代谢及甲氨蝶呤反应影响的31P核磁共振研究
NMR Biomed. 1989 Jun;2(1):12-8. doi: 10.1002/nbm.1940020104.
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Alterations in serum levels, anti-tumor activity and toxicity of methotrexate in rats after a short period of nutritional depletion.短期营养缺乏后大鼠血清中甲氨蝶呤水平、抗肿瘤活性及毒性的变化
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Host and tumor responses to varying rates of nitrogen infusion in the tumor-bearing rat.荷瘤大鼠对不同氮输注速率的宿主和肿瘤反应。
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Influence of reducing luxury calories in the treatment of experimental mammary carcinoma.减少奢侈热量摄入对实验性乳腺癌治疗的影响。
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本文引用的文献

1
The influence of diet on the Walker rat carcinoma 256, and its response to x-radiation; cytological and histological investigations.饮食对沃克大鼠癌256的影响及其对X射线的反应;细胞学和组织学研究。
Br J Cancer. 1950 Sep;4(3):298-314. doi: 10.1038/bjc.1950.28.
2
Metabolic observations during the forced feeding of patients with cancer.癌症患者强制喂食期间的代谢观察。
Am J Med. 1956 Feb;20(2):225-38. doi: 10.1016/0002-9343(56)90193-0.
3
Nutrition in relation to cancer.与癌症相关的营养
Adv Cancer Res. 1953;1:451-501. doi: 10.1016/s0065-230x(08)60009-3.
4
Potentiation of solid-tumor chemotherapy by metabolic alteration.通过代谢改变增强实体瘤化疗效果
Ann Surg. 1974 Jan;179(1):88-93. doi: 10.1097/00000658-197401000-00017.
5
Limited capacity for motor activity as a cause for declining food intake in cancer.运动能力受限作为癌症患者食物摄入量下降的一个原因。
J Natl Cancer Inst. 1973 Nov;51(5):1535-9. doi: 10.1093/jnci/51.5.1535.
6
Intravenous hyperalimentation in cancer patients.癌症患者的静脉高营养疗法
J Surg Res. 1974 Mar;16(3):241-7. doi: 10.1016/0022-4804(74)90038-9.
7
The cell cycle and its significance for cancer treatment.
Cancer Treat Rev. 1975 Sep;2(3):159-75. doi: 10.1016/s0305-7372(75)80001-6.
8
DNA synthesis in rat sarcoma and liver: the effect of starvation.大鼠肉瘤和肝脏中的DNA合成:饥饿的影响。
J Surg Res. 1977 Mar;22(3):281-6. doi: 10.1016/0022-4804(77)90144-5.
9
Effects of nutrition on tumor growth and tolerance to chemotherapy.营养对肿瘤生长及化疗耐受性的影响。
J Surg Res. 1975 Apr;18(4):455-66. doi: 10.1016/0022-4804(75)90109-2.
10
Intravenous hyperalimentation as an adjunct to cancer chemotherapy with 5-fluorouracil.静脉高营养作为5-氟尿嘧啶癌症化疗的辅助手段。
J Surg Res. 1975 Apr;18(4):451-4. doi: 10.1016/0022-4804(75)90108-0.

实验动物中的肿瘤生长:大鼠的营养调控与化疗反应

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

作者信息

Daly J M, Reynolds H M, Rowlands B J, Dudrick S J, Copeland E M

出版信息

Ann Surg. 1980 Mar;191(3):316-22. doi: 10.1097/00000658-198003000-00010.

DOI:10.1097/00000658-198003000-00010
PMID:7362297
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1344702/
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.

摘要

在患有Walker-256癌肉瘤的Sprague-Dawley大鼠中,研究了营养调控对宿主体重动态变化、肿瘤生长模式以及宿主-肿瘤对化疗反应的影响。第一组大鼠自始至终维持常规饮食(RD),其胴体重量稳步增加。第二组大鼠在喂食无蛋白饮食(PFD)期间胴体重量减轻,但在第15天改回RD后体重迅速增加。从第15天到21天,第一组大鼠的平均肿瘤体积增加了105%,第二组增加了218%,第三组增加了77%(继续喂食PFD,p<0.05)。从第21天到第33天,第一组和第二组大鼠的肿瘤生长模式相似,而第三组大鼠的平均肿瘤体积最终趋于平稳。在研究B中,第二组动物在从PFD改为RD后的第二天和第六天给予甲氨蝶呤(MTX-20mg/kg)。MTX处理大鼠的肿瘤体积平均变化为1.31±0.1cm³,而生理盐水处理的对照大鼠为8.14±0.1cm³(p<0.001)。MTX对第三组(PFD)大鼠的肿瘤生长模式没有显著影响。在研究A中,蛋白质-热量营养不良导致宿主胴体重量减轻和肿瘤生长迟缓,而营养补充恢复了宿主胴体重量并刺激了肿瘤生长。在研究B中,MTX对从PFD改为RD的荷瘤大鼠效果最佳,表明营养调控可以改善宿主营养状况并增强肿瘤对化疗的反应。