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鱼油和他莫昔芬对 N-甲基-N-亚硝脲诱导的大鼠乳腺癌发生早期前瘤病变发展和氧化应激生物标志物的影响。

Effects of fish oil and Tamoxifen on preneoplastic lesion development and biomarkers of oxidative stress in the early stages of N-methyl-N-nitrosourea-induced rat mammary carcinogenesis.

机构信息

Division of Endocrinology, H044, Hershey Medical Center, Hershey, PA 17033, USA.

出版信息

Int J Oncol. 2011 Nov;39(5):1153-64. doi: 10.3892/ijo.2011.1133. Epub 2011 Jul 20.

Abstract

Epidemiologic studies on the protective role of omega-3 fatty acids (n:3) on breast cancer prevention remain inconclusive but studies in preclinical models provide more positive outcome. However, the mechanisms accounting for the protective effect of n:3 are not defined. In the present study, conducted in the N-methyl-N-nitrosourea-induced rat mammary carcinogenesis model, we examined the effects of n:3 individually and in combination with the anti-estrogen Tamoxifen (Tam) on a comprehensive panel of systemic and preneoplastic mammary gland restricted biomarkers which may be critical in the progression to invasive cancer. We observed that fish oil (FO) rich diets significantly reduced Ki67 expression in hyperplastic lesions, while cleaved caspase-3 expression was not affected. Dietary FO and/or Tam did not have major effects on systemic oxidative stress biomarkers, based on oxidative damage to DNA measured as 8-hydroxy-2-deoxyguanosine (8-OH-dG) and lipid peroxidation assessed as thiobarbituric acid reactive substances (TBARS). Tissue levels of 8-isoprostane, on the other hand, were markedly reduced (p<0.0001) in FO-fed rats, possibly as a result of FO-induced depletion of arachidonic acid in the mammary gland. These results suggest that the protective effect of n:3 in this experimental system is not mediated by changes in the levels of oxidative stress but may result from suppression of arachidonic acid-specific pathways.

摘要

关于 ω-3 脂肪酸(n:3)对乳腺癌预防的保护作用的流行病学研究仍不确定,但临床前模型研究提供了更积极的结果。然而,n:3 保护作用的机制尚未确定。在本研究中,我们在 N-甲基-N-亚硝脲诱导的大鼠乳腺致癌模型中,检查了 n:3 单独和与抗雌激素他莫昔芬(Tam)联合使用对系统和乳腺前病变限制生物标志物的全面研究,这些标志物在进展为侵袭性癌症中可能是关键的。我们观察到,富含鱼油(FO)的饮食显著降低了增生性病变中的 Ki67 表达,而裂解的 caspase-3 表达不受影响。基于 8-羟基-2-脱氧鸟苷(8-OH-dG)测量的 DNA 氧化损伤和作为硫代巴比妥酸反应物质(TBARS)评估的脂质过氧化,膳食 FO 和/或 Tam 对系统氧化应激生物标志物没有重大影响。另一方面,组织水平的 8-异前列腺素明显降低(p<0.0001)在 FO 喂养的大鼠中,这可能是由于 FO 诱导的乳腺中花生四烯酸耗竭所致。这些结果表明,n:3 在该实验系统中的保护作用不是通过改变氧化应激水平介导的,而是可能源于对花生四烯酸特异性途径的抑制。

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