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在喂食缺乏胆碱饮食的雄性费希尔大鼠的肝脏DNA以及由此产生的肿瘤DNA中,内源性DNA修饰(I-化合物)水平持续降低。

Persistent reduction of indigenous DNA modification (I-compound) levels in liver DNA from male Fischer rats fed choline-devoid diet and in DNA of resulting neoplasms.

作者信息

Li D H, Xu D C, Chandar N, Lombardi B, Randerath K

机构信息

Department of Pharmacology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Cancer Res. 1990 Dec 1;50(23):7577-80.

PMID:2253208
Abstract

Reduced levels of putative indigenous DNA modifications (I-compounds) in liver DNA of male Fischer 344 rats fed a hepatocarcinogenic choline-devoid (CD) diet for up to 7 mo have been previously reported. To investigate the persistence of this effect and possible relationships between I-compounds and hepatocarcinogenesis, liver DNA modifications of tumor-free male rats fed a CD diet for 3, 6, 9, or 12 mo, followed by a choline-supplemented (CS) diet to 16 mo, were compared with those in rats fed exclusively the CD or CS diet for 16 mo by a 32P-postlabeling assay. In addition, DNA from nontumorous and tumorous tissues of rats fed the CD diet similarly for 12 or 16 mo was analyzed. It was found that total I-compound levels in male rats consecutively fed CD and CS diets for various lengths of time were similar to those in rats fed the CD diet only and significantly lower than those in rats fed the CS diet only. I-compound levels of nontumorous regions from tumor-bearing livers were 73% of those in tumor-free livers from the same treatment group. I-compound levels were further reduced, some to undetectable levels, in tumor tissues and exhibited an inverse relationship with tumor incidence. The patterns and levels of I-compounds in liver DNA of CD diet-fed female rats, which were not susceptible to CD diet-induced hepatocarcinogenesis, on the other hand, were not significantly different from those of controls. Thus, reduction of I-compound levels by feeding a CD diet lasted for many months after changing from the CD to the CS diet. Whether this persistent DNA alteration contributes to carcinogenesis remains to be determined.

摘要

先前有报道称,给雄性Fischer 344大鼠喂食致肝癌的无胆碱(CD)饮食长达7个月,其肝脏DNA中假定的内源性DNA修饰(I-化合物)水平会降低。为了研究这种效应的持续性以及I-化合物与肝癌发生之间的可能关系,通过32P后标记分析法,将喂食CD饮食3、6、9或12个月,随后喂食补充胆碱(CS)饮食至16个月的无肿瘤雄性大鼠的肝脏DNA修饰,与仅喂食CD或CS饮食16个月的大鼠进行了比较。此外,还分析了同样喂食CD饮食12或16个月的大鼠非肿瘤组织和肿瘤组织的DNA。结果发现,连续喂食不同时长的CD和CS饮食的雄性大鼠中,I-化合物的总水平与仅喂食CD饮食的大鼠相似,且显著低于仅喂食CS饮食的大鼠。荷瘤肝脏非肿瘤区域的I-化合物水平是同一治疗组无肿瘤肝脏I-化合物水平的73%。I-化合物水平在肿瘤组织中进一步降低,有些降至检测不到的水平,并且与肿瘤发生率呈负相关。另一方面,不易受到CD饮食诱导肝癌发生影响的喂食CD饮食的雌性大鼠肝脏DNA中I-化合物的模式和水平与对照组无显著差异。因此,从CD饮食改为CS饮食后,通过喂食CD饮食降低I-化合物水平的情况会持续数月。这种持续的DNA改变是否会导致癌症发生仍有待确定。

相似文献

1
Persistent reduction of indigenous DNA modification (I-compound) levels in liver DNA from male Fischer rats fed choline-devoid diet and in DNA of resulting neoplasms.在喂食缺乏胆碱饮食的雄性费希尔大鼠的肝脏DNA以及由此产生的肿瘤DNA中,内源性DNA修饰(I-化合物)水平持续降低。
Cancer Res. 1990 Dec 1;50(23):7577-80.
2
Stimulation of DNA synthesis and cell proliferation in the liver of rats fed a choline-devoid diet and their suppression by phenobarbital.喂食缺乏胆碱饮食的大鼠肝脏中DNA合成和细胞增殖的刺激作用以及苯巴比妥对其的抑制作用。
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Enhancement of DL-ethionine-induced liver carcinogenesis in rats fed a choline-devoid diet.在喂食缺乏胆碱饮食的大鼠中,DL-乙硫氨酸诱导的肝癌发生增强。
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Nuclear DNA content of altered hepatic foci in a rat liver carcinogenesis model.大鼠肝癌发生模型中肝脏改变灶的核DNA含量
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Endogenous hepatic growth-modulating factors and effects of a choline-devoid diet and of phenobarbital on hepatocarcinogenesis in the rat.内源性肝脏生长调节因子以及缺乏胆碱饮食和苯巴比妥对大鼠肝癌发生的影响。
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Early histological and functional alterations of ethionine liver carcinogenesis in rats fed a choline-deficient diet.在喂食胆碱缺乏饮食的大鼠中,乙硫氨酸诱导肝癌发生的早期组织学和功能改变。
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No enhancement by phenobarbital of the hepatocarcinogenicity of a choline-devoid diet in the rat.苯巴比妥对大鼠缺乏胆碱饮食所致肝癌致癌性无增强作用。
Res Commun Chem Pathol Pharmacol. 1990 Aug;69(2):197-207.

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