Schwarz M, Peres G, Beer D G, Maor M, Buchmann A, Kunz W, Pitot H C
Cancer Res. 1986 Nov;46(11):5903-12.
The process of chemical hepatocarcinogenesis is characterized by the appearance of preneoplastic lesions showing changes in the expression of various marker enzymes. We have analyzed the phenotype of small preneoplastic foci and expansively growing nodules in liver sections obtained from rats treated with various carcinogens. Changes within the lesions in canalicular adenosine triphosphatase, gamma-glutamyl transpeptidase, NADPH-(cytochrome P-450) reductase, cytochrome P-450 PB2, epoxide hydrolase, and glycogen content were detected by means of enzyme histochemical and immunohistochemical staining procedures. In parallel sections the expression of albumin messenger RNA was investigated by in situ hybridization using a 35S-labeled albumin specific complementary DNA probe. In general, small preneoplastic lesions showed unchanged levels of albumin messenger RNA. In contrast, the expression of albumin messenger RNA was found to be reduced to varying degrees in large hepatic nodules. An expression of alpha-fetoprotein messenger RNA could not be detected in any of the nodules. No direct correlation between the enzyme phenotype of the lesions and the degree in reduction of albumin messenger RNA could be established except that the reduction was most pronounced in nodules which had lost their ability to store glycogen. Since the synthesis and excretion of albumin is a typical function of the differentiated hepatocyte in the adult animal, the observed decrease in albumin messenger RNA expression in large hepatic nodules is in accordance with the hypothesis of a gradual dedifferentiation or retrodifferentiation of the cell population during carcinogenesis. Hyperplastic nodules produced by continuous treatment of rats with 4-dimethylaminoazobenzene showed increased rather than decreased albumin levels. The analysis of albumin messenger RNA expression might therefore be used as a tool to discriminate between nodules of differing biological nature and fate.
化学性肝癌发生过程的特征是出现癌前病变,这些病变表现为各种标记酶表达的变化。我们分析了用各种致癌物处理的大鼠肝脏切片中微小癌前病灶和扩展性生长结节的表型。通过酶组织化学和免疫组织化学染色程序检测了胆小管三磷酸腺苷酶、γ-谷氨酰转肽酶、NADPH-(细胞色素P-450)还原酶、细胞色素P-450 PB2、环氧化物水解酶和糖原含量在病变内的变化。在平行切片中,使用35S标记的白蛋白特异性互补DNA探针通过原位杂交研究白蛋白信使RNA的表达。一般来说,微小癌前病变的白蛋白信使RNA水平未发生变化。相比之下,在大的肝结节中发现白蛋白信使RNA的表达不同程度地降低。在任何结节中均未检测到甲胎蛋白信使RNA的表达。除了在已失去储存糖原能力的结节中白蛋白信使RNA的降低最为明显外,病变的酶表型与白蛋白信使RNA的降低程度之间未建立直接相关性。由于白蛋白的合成和分泌是成年动物分化肝细胞的典型功能,因此在大的肝结节中观察到的白蛋白信使RNA表达降低与癌变过程中细胞群体逐渐去分化或逆分化的假说是一致的。用4-二甲基氨基偶氮苯持续处理大鼠产生的增生性结节显示白蛋白水平升高而非降低。因此,白蛋白信使RNA表达的分析可作为区分具有不同生物学性质和命运的结节的一种工具。