Oyaizu N, Morii S, Saito K, Katsuda Y, Matsumoto J
Jpn J Cancer Res. 1985 Aug;76(8):676-83.
The mechanism of growth enhancement of 7,12-dimethylbenz[a]anthracene (DMBA)-induced mammary tumors by high fat diet was investigated in 169 female Sprague-Dawley rats fed a semisynthetic diet containing 0, 8 or 40% corn oil by weight. The animals, most of which were intubated with 10 mg of DMBA twice during the 8th week of age, were fed an unsupplemented or fat-supplemented diet for 2 months from the 12th to the 21st week of age and finally killed during the 21st week of age. Compared to the rats fed a fat-free diet, a significantly increased yield of mammary adenocarcinoma with a shorter latency was observed in the rats fed a 40% corn oil diet. DNA synthesis of the biopsied mammary tumors more than 1 month after diet switch-over was estimated in terms of the rate of [3H]thymidine incorporation into the tissue. Significantly higher DNA synthesis of the mammary tumors biopsied from proestrous hosts was found, as compared with the tumors in similar hosts at other stages of the estrous cycle. The greatest enhancement of DNA synthesis in small and rapidly growing tumors was observed in the 40% corn oil diet group. Feeding with 40% corn oil diet always resulted in elevation of the weight percentage of linoleic acid in both simple lipids and phospholipids of the mammary tumors. These data indicate that the effects of dietary fat on mammary tumor growth might be mediated by the enhancement of tumor response to certain hormones, and that the enhanced responsiveness of tumors was associated with increased linoleic acid in tumor lipids.
在169只雌性斯普拉格-道利大鼠中研究了高脂饮食促进7,12-二甲基苯并[a]蒽(DMBA)诱导的乳腺肿瘤生长的机制,这些大鼠喂食含0%、8%或40%(重量)玉米油的半合成饮食。大多数动物在8周龄时两次经插管给予10mg DMBA,从12周龄到21周龄喂食未补充脂肪或补充脂肪的饮食,最后在21周龄时处死。与喂食无脂肪饮食的大鼠相比,喂食40%玉米油饮食的大鼠乳腺腺癌的产量显著增加,潜伏期缩短。根据[3H]胸腺嘧啶掺入组织的速率估计饮食转换1个月后活检乳腺肿瘤的DNA合成。与处于发情周期其他阶段的类似宿主中的肿瘤相比,发现从发情前期宿主活检的乳腺肿瘤的DNA合成显著更高。在40%玉米油饮食组中观察到小的快速生长肿瘤的DNA合成增强最大。喂食40%玉米油饮食总是导致乳腺肿瘤的简单脂质和磷脂中亚油酸的重量百分比升高。这些数据表明,饮食脂肪对乳腺肿瘤生长的影响可能是通过增强肿瘤对某些激素的反应来介导的,并且肿瘤反应性增强与肿瘤脂质中亚油酸增加有关。