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免疫组织化学法证实了葡萄糖-6-磷酸脱氢酶、γ-谷氨酰转肽酶、鸟氨酸脱羧酶和谷胱甘肽S-转移酶:在大鼠肝脏假定的癌前病变中与细胞增殖无直接相关性。

Immunohistochemically demonstrated glucose-6-phosphate dehydrogenase, gamma-glutamyl transpeptidase, ornithine decarboxylase and glutathione S-transferase enzymes: absence of direct correlation with cell proliferation in rat liver putative pre-neoplastic lesions.

作者信息

Moore M A, Nakamura T, Ito N

出版信息

Carcinogenesis. 1986 Sep;7(9):1419-24. doi: 10.1093/carcin/7.9.1419.

DOI:10.1093/carcin/7.9.1419
PMID:2874898
Abstract

Comparison of binding of specific antibodies to glucose-6-phosphate dehydrogenase (G6PD), gamma-glutamyl transpeptidase (GT), ornithine decarboxylase (ODC) and the glutathione S-transferase B and P forms (GST-B, P) was made in putative pre-neoplastic lesions during their induction and subsequent development using the Solt-Farber model. The earliest focal hepatocellular lesions were evident as single, or small groups of GST-P-positive hepatocytes in tissue taken at partial hepatectomy 3 weeks after initial application of diethylnitrosamine (DEN). With the onset of proliferation and increase in size the majority of the lesions expressed elevated levels of all of the enzyme proteins investigated with a correlation between strength of binding and morphology being apparent. While [3H]thymidine incorporation was limited during the period of acetylaminofluorene administration, to the hepatocytes demonstrating altered enzyme phenotype no direct link between proliferation rate within individual foci and level of G6PD expression could be discerned. Similarly, the elevated level of labelling characteristic of persisting nodular lesions at later stages also did not correlate with degree of G6PD alteration in individual cells. The results indicate that while changed enzyme phenotype appears as an ordered pattern suggestive of physiological adaptive nature, the degree of alteration is not directly related to proliferation kinetics under the rapid induction conditions characteristic of the Solt-Farber model.

摘要

利用索尔特-法伯模型,对特定抗体与葡萄糖-6-磷酸脱氢酶(G6PD)、γ-谷氨酰转肽酶(GT)、鸟氨酸脱羧酶(ODC)以及谷胱甘肽S-转移酶B和P型(GST-B、P)的结合情况进行了比较,研究对象为推定的癌前病变在诱导及后续发展过程中的情况。最早的局灶性肝细胞病变表现为在初次应用二乙基亚硝胺(DEN)3周后进行部分肝切除所取组织中单个或小群GST-P阳性肝细胞。随着增殖的开始和大小的增加,大多数病变表达了所有研究的酶蛋白的升高水平,结合强度与形态之间的相关性明显。虽然在给予乙酰氨基芴期间[3H]胸腺嘧啶核苷掺入仅限于表现出改变的酶表型的肝细胞,但在各个病灶内的增殖率与G6PD表达水平之间未发现直接联系。同样,后期持续存在的结节性病变的特征性标记升高水平也与单个细胞中G6PD改变程度无关。结果表明,虽然改变的酶表型呈现出一种有序模式,提示具有生理适应性,但在索尔特-法伯模型的快速诱导条件下,改变程度与增殖动力学没有直接关系。

相似文献

1
Immunohistochemically demonstrated glucose-6-phosphate dehydrogenase, gamma-glutamyl transpeptidase, ornithine decarboxylase and glutathione S-transferase enzymes: absence of direct correlation with cell proliferation in rat liver putative pre-neoplastic lesions.免疫组织化学法证实了葡萄糖-6-磷酸脱氢酶、γ-谷氨酰转肽酶、鸟氨酸脱羧酶和谷胱甘肽S-转移酶:在大鼠肝脏假定的癌前病变中与细胞增殖无直接相关性。
Carcinogenesis. 1986 Sep;7(9):1419-24. doi: 10.1093/carcin/7.9.1419.
2
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3
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引用本文的文献

1
Number of simultaneously expressed enzyme alterations correlates with progression of N-ethyl-N-hydroxyethylnitrosamine-induced hepatocarcinogenesis in rats.同时表达的酶改变数量与N-乙基-N-羟乙基亚硝胺诱导的大鼠肝癌发生进展相关。
Jpn J Cancer Res. 1993 Dec;84(12):1237-44. doi: 10.1111/j.1349-7006.1993.tb02828.x.
2
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.
3
MTrasT24, a metallothionein-ras fusion gene, modulates expression in cultured rat liver cells of two genes associated with in vivo liver cancer.
MTrasT24是一种金属硫蛋白-ras融合基因,可调节培养的大鼠肝细胞中与体内肝癌相关的两个基因的表达。
Proc Natl Acad Sci U S A. 1988 Jan;85(2):344-8. doi: 10.1073/pnas.85.2.344.
4
Enzymes of glutathione metabolism as biochemical markers during hepatocarcinogenesis.谷胱甘肽代谢酶作为肝癌发生过程中的生化标志物。
Cancer Metastasis Rev. 1987;6(2):155-78. doi: 10.1007/BF00052847.
5
Effects of modifying agents on conformity of enzyme phenotype and proliferative potential in focal preneoplastic and neoplastic liver cell lesions in rats.修饰剂对大鼠局灶性癌前和肿瘤性肝细胞病变中酶表型一致性及增殖潜能的影响。
Jpn J Cancer Res. 1992 Nov;83(11):1154-65. doi: 10.1111/j.1349-7006.1992.tb02739.x.