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饮食脂肪或他莫昔芬对甲基亚硝基脲处理的大鼠乳腺中携带Ha-ras癌基因的细胞扩增的影响。

Effect of dietary fat or tamoxifen on the expansion of cells harboring Ha-ras oncogenes in mammary glands from methylnitrosourea-treated rats.

作者信息

Hu Z, Chaulk J E, Lu S J, Xu Z, Archer M C

机构信息

Department of Medical Biophysics, University of Toronto, Canada.

出版信息

Carcinogenesis. 1995 Sep;16(9):2281-4. doi: 10.1093/carcin/16.9.2281.

Abstract

Diets containing high levels of fat enhance the formation of methylnitrosourea (MNU)-induced mammary gland adenocarcinomas in rats, while administration of the antiestrogen tamoxifen decreases the incidence of these tumors. It is not known, however, at what stage during tumor development the fat or tamoxifen exert their effects. Here we have used a PCR/liquid hybridization and gel retardation assay to determine the effects of dietary fat and tamoxifen on the growth rate of cells harboring an Ha-ras oncogene in the mammary glands of rats at various times following MNU administration. Glands from animals on a high-fat diet had significantly higher mutant cell fractions than those on a low-fat diet at both 30 and 75 days following MNU treatment. In contrast, there was no difference between the mutant cell fractions of tamoxifen-treated animals and controls at either 30 or 70 days. These results suggest that dietary fat promotes tumor formation early in carcinogenesis by stimulating the growth of cells harboring Ha-ras mutations, while tamoxifen delays the appearance of tumors either by acting as a tumoristatic or tumoricidal agent, or by acting to eliminate or retard the growth of preneoplastic cells just prior to the emergence of tumors.

摘要

高脂肪饮食会促进甲基亚硝基脲(MNU)诱导的大鼠乳腺腺癌的形成,而给予抗雌激素他莫昔芬会降低这些肿瘤的发生率。然而,尚不清楚脂肪或他莫昔芬在肿瘤发展的哪个阶段发挥作用。在此,我们使用聚合酶链反应/液相杂交和凝胶阻滞分析,来确定在给予MNU后的不同时间,饮食脂肪和他莫昔芬对大鼠乳腺中携带Ha-ras癌基因的细胞生长速率的影响。在MNU处理后的30天和75天,高脂饮食动物的腺体中突变细胞分数显著高于低脂饮食动物。相比之下,在30天或70天时,他莫昔芬处理动物与对照动物的突变细胞分数没有差异。这些结果表明,饮食脂肪通过刺激携带Ha-ras突变的细胞生长,在致癌早期促进肿瘤形成,而他莫昔芬通过作为肿瘤抑制或杀伤剂发挥作用,或者通过在肿瘤出现之前消除或延缓肿瘤前体细胞的生长来延迟肿瘤的出现。

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