Fischer S M, Leyton J, Lee M L, Locniskar M, Belury M A, Maldve R E, Slaga T J, Bechtel D H
University of Texas M.D. Anderson Cancer Center, Research Division, Smithville 78957.
Cancer Res. 1992 Apr 1;52(7 Suppl):2049s-2054s.
On the basis of reports of rat mammary- and pancreas-tumor models, we hypothesized that an increase in consumption of linoleic acid (LA) would also cause an enhancement in mouse skin-tumor promotion. SEN-CAR mice were placed on diets containing 0.8%, 2.2%, 3.5%, 4.5%, 5.6%, 7.0%, or 8.4% LA, 1 week after initiation with 7,12-dimethylbenz(a)anthracene and 3 weeks before starting promotion with 12-O-tetradecanoylphorbol-13-acetate. An inverse correlation (r = -0.92) was observed between papilloma number and level of LA; however, there was little difference in tumor incidence. A relationship between diet and carcinoma incidence was also found. The fatty acid composition of epidermal phospholipids reflected the dietary LA levels. 12-O-Tetradecanoylphorbol-13-acetate-induced epidermal prostaglandin E2 levels generally decreased with increasing dietary LA. To determine whether this inverse correlation between dietary LA and tumor yield was due to species differences or organ-model differences, a mammary carcinogenesis experiment was performed. SENCAR mice were fed the 0.8%, 4.5%, and 8.4% LA diets. All mice received 6 mg 7,12-dimethylbenz(a)anthracene, administered intragastrically at 1 mg/week. Tumor appearance was delayed in the 0.8% LA diet group, and a positive dose-response relationship between dietary LA and mammary-tumor incidence was observed. These studies suggest that the effect of dietary LA on tumor development is target tissue specific rather than species specific.
基于大鼠乳腺和胰腺肿瘤模型的报告,我们推测亚油酸(LA)摄入量的增加也会导致小鼠皮肤肿瘤促进作用增强。在用7,12-二甲基苯并(a)蒽启动1周后,以及在用12-O-十四烷酰佛波醇-13-乙酸酯开始促进前3周,将SEN-CAR小鼠置于含有0.8%、2.2%、3.5%、4.5%、5.6%、7.0%或8.4%LA的饮食中。观察到乳头状瘤数量与LA水平之间呈负相关(r = -0.92);然而,肿瘤发生率几乎没有差异。还发现了饮食与癌发生率之间的关系。表皮磷脂的脂肪酸组成反映了饮食中的LA水平。随着饮食中LA的增加,12-O-十四烷酰佛波醇-13-乙酸酯诱导的表皮前列腺素E2水平通常会降低。为了确定饮食中LA与肿瘤产量之间的这种负相关是由于物种差异还是器官模型差异,进行了一项乳腺癌发生实验。给SENCAR小鼠喂食0.8%、4.5%和8.4%LA的饮食。所有小鼠每周接受6毫克7,12-二甲基苯并(a)蒽,通过胃内给药,剂量为1毫克/周。在0.8%LA饮食组中肿瘤出现延迟,并且观察到饮食中LA与乳腺肿瘤发生率之间存在正剂量反应关系。这些研究表明,饮食中LA对肿瘤发展的影响是靶组织特异性的,而不是物种特异性的。