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大鼠肝脏短期系统中诱导产生的局灶性和结节性病变的表型不稳定性

Phenotypic instability in focal and nodular lesions induced in a short term system in the rat liver.

作者信息

Moore M A, Hacker H J, Bannasch P

出版信息

Carcinogenesis. 1983;4(5):595-603. doi: 10.1093/carcin/4.5.595.

DOI:10.1093/carcin/4.5.595
PMID:6850991
Abstract

A comparative morphologic, morphometric and enzyme histochemical investigation of lesions induced by short-term application of N-nitrosomorpholine (NNM) and subsequent so-called 'selection pressure' was carried out in order to assess the characteristics of the numbers of induced putative preneoplastic populations and to cast light on reversibility associated with this model. The glycogen storage foci, mixed cell foci and neoplastic nodules observed after 'selection pressure' were in principle similar to those seen after stop experiments, although alterations in morphology and enzyme phenotype of individual cells were usually far more pronounced after short-term induction. It was established that 75% of the lesions were no longer visible 11 weeks after withdrawal of induction stimuli and that a large proportion of these remaining demonstrated heterogeneity in morphological and histochemical markers indicative of reversion to normal phenotype. After a further 10 weeks a slight increase in number of foci associated with decrease in size and enhanced homogeneity in phenotypic markers was established. The behaviour of foci and nodules undergoing reversion was considered with respect to changes in basophilia and glycogen storage and activity of the enzymes glucose-6-phosphate dehydrogenase, glucose-6-phosphatase, glyceraldehyde 3-phosphate dehydrogenase, glycogen phosphorylase and synthase, acid phosphatase and gamma-glutamyl transpeptidase and correlated with location of altered cellular populations within the liver functional acinus.

摘要

为了评估诱导产生的假定癌前细胞群数量的特征,并阐明与该模型相关的可逆性,我们对短期应用N-亚硝基吗啉(NNM)及随后的所谓“选择压力”所诱导的病变进行了比较形态学、形态计量学和酶组织化学研究。“选择压力”后观察到的糖原储存灶、混合细胞灶和肿瘤结节原则上与停止实验后所见相似,尽管短期诱导后单个细胞的形态和酶表型改变通常更为明显。已确定在撤除诱导刺激11周后,75%的病变不再可见,并且这些剩余病变中有很大一部分在形态学和组织化学标记物方面表现出异质性,表明其向正常表型逆转。再过10周后,发现灶的数量略有增加,同时灶的大小减小,表型标记物的同质性增强。针对嗜碱性、糖原储存以及葡萄糖-6-磷酸脱氢酶、葡萄糖-6-磷酸酶、甘油醛-3-磷酸脱氢酶、糖原磷酸化酶和合成酶、酸性磷酸酶和γ-谷氨酰转肽酶的活性变化,对发生逆转的灶和结节的行为进行了研究,并将其与肝功能性腺泡内细胞群改变的位置相关联。

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Phenotypic instability in focal and nodular lesions induced in a short term system in the rat liver.大鼠肝脏短期系统中诱导产生的局灶性和结节性病变的表型不稳定性
Carcinogenesis. 1983;4(5):595-603. doi: 10.1093/carcin/4.5.595.
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引用本文的文献

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Letter.信件。
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Characteristic upregulation of glucose-regulated protein 78 in an early lesion negative for hitherto established cytochemical markers in rat hepatocarcinogenesis.在大鼠肝癌发生过程中,对于迄今已确立的细胞化学标志物呈阴性的早期病变中,葡萄糖调节蛋白78的特征性上调。
J Toxicol Pathol. 2009 Dec;22(4):281-8. doi: 10.1293/tox.22.281. Epub 2009 Dec 21.
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alpha(2)-Macroglobulin: a novel cytochemical marker characterizing preneoplastic and neoplastic rat liver lesions negative for hitherto established cytochemical markers.
α(2)-巨球蛋白:一种新型细胞化学标志物,用于表征对迄今已确立的细胞化学标志物呈阴性的大鼠肝肿瘤前病变和肿瘤性病变。
Am J Pathol. 2004 Nov;165(5):1479-88. doi: 10.1016/s0002-9440(10)63406-2.
4
Sequential cellular changes during chemical carcinogenesis.化学致癌过程中的细胞序列变化。
J Cancer Res Clin Oncol. 1984;108(1):11-22. doi: 10.1007/BF00390968.
5
Tumor promotion in the liver.肝脏中的肿瘤促进作用。
Arch Toxicol. 1985 Aug;57(3):147-58. doi: 10.1007/BF00290879.
6
Non-persisting early foci of altered hepatocytes induced in rats by N-nitrosomorpholine.由N-亚硝基吗啉诱导的大鼠肝脏中出现的非持续性早期肝细胞改变灶。
J Cancer Res Clin Oncol. 1988;114(1):30-4. doi: 10.1007/BF00390482.
7
Glutathione S-transferases and hepatocarcinogenesis.谷胱甘肽S-转移酶与肝癌发生
Jpn J Cancer Res. 1988 May;79(5):556-72. doi: 10.1111/j.1349-7006.1988.tb00022.x.
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Concentration-dependent inhibition of development of GGT positive foci in rat liver by the environmental contaminant di(2-ethylhexyl) phthalate.环境污染物邻苯二甲酸二(2-乙基己基)酯对大鼠肝脏中γ-谷氨酰转肽酶阳性病灶发展的浓度依赖性抑制作用。
Environ Health Perspect. 1985 May;60:381-5. doi: 10.1289/ehp.8560381.
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Environ Health Perspect. 1991 Jun;93:181-9. doi: 10.1289/ehp.9193181.