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EARLY EVENTS IN CHEMICALLY INDUCED RAT HEPATOCARCINOGENESIS

EARLY EVENTS IN CHEMICALLY INDUCED RAT HEPATOCARCINOGENESIS
化学诱导的大鼠肝癌的早期事件
批准号:
3963468
负责人:
P J WIRTH
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至

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中文摘要
翻译
该项目的启动是为了研究化学过程中的事件顺序, 使用啮齿类动物肝癌模型联合 定量双向凝胶电泳(2D-PAGE)。 结果 迄今为止获得的结果包括:(1)分析 正常大鼠肝脏和肿瘤前和肿瘤结节产生, Solt-Farber方案(“抗性肝细胞”模型)或通过 喂食过氧化物酶体增殖的非遗传毒性诱导剂,环丙贝特, 揭示了很少的定性但大量的定量多肽差异; (2)个体肿瘤前和肿瘤中的多肽表达 通过Solt-Farber方案或环丙贝特诱导的结节非常 类似,表明一个显着的“同质性”,而不是“异质性”的 多肽表达的早期病变;(3)所有Solt-Farber 生成的结节对γ-谷氨酰转肽酶和 (GGT)活性和胎盘型谷胱甘肽-S-转移酶 (GST-P),而在环丙贝特诱导的结节中,GGT的表达 与对照组相比,sGST-P无显著性差异; 在Solt-Farber诱导的细胞中观察到四种定性多肽差异, 与正常肝脏相比。 其中两种,多肽B(pI pI 6.75/24 kDa)和C(pI 6.25/41 kDa)在两种细胞中均有表达。 环丙贝特诱导的和Solt-Farber产生的癌前病变和肿瘤 结节 此外,五种膜相关蛋白(5.25/59 kDa,5/30/33 kDa, 5.25/27 kDa、6.82/23.5 kDa和6.75/21 kDa)和四种细胞溶质 多肽(6.20/45 kDa,5/85/36 kDa,5.06/34 kDa,6.00/24 kDa)是 在肿瘤前和肿瘤结节中协调表达, 环丙贝特和Solt-Farber肝癌发生模型。
英文摘要
The project was initiated to study the sequence of events during chemically induced neoplasia using the rodent hepatoma model in combination with quantitative two-dimensional gel electrophoresis (2D-PAGE). Results obtained to date include: (1) analysis of polypeptide differences between normal rat liver and preneoplastic and neoplastic nodules generated using either the Solt-Farber regimen ("resistant hepatocyte" model) or via feeding the nongenotoxic inducer of peroxisome proliferation, ciprofibrate, revealed few qualitative but numerous quantitative polypeptide differences; (2) polypeptide expression in individual preneoplastic and neoplastic nodules induced via the Solt-Farber protocol or with ciprofibrate was very similar, suggesting a marked "homogeneity" rather than "heterogeneity" of polypeptide expression among the early lesions; (3) all Solt-Farber generated nodules stained strongly both for gamma-gutamyltranspeptidase (GGT) activity and for the placental form of glutathione-S-transferase (GST-P), while in the ciprofibrate induced nodules the expression of GGT and s GST-P was not significantly different than control liver levels; (4) four qualitative polypeptide differnces were noted in Solt-Farber-induced nodules as compared to normal liver. Two of these, polypeptides B (pI 6.25/41 kDa) and C (pI 6.75/24 kDa) were expressed in both ciprofibrate-induced and Solt-Farber-generated preneoplastic and neoplastic nodules. In addition five membrane-associated (5.25/59 kDa, 5/30/33 kDa, 5.25/27 kDa, 6.82/23.5 kDa, and 6.75/21 kDa) and four cytosolic polypeptides (6.20/45 kDa, 5/85/36 kDa, 5.06/34 kDa, 6.00/24 kDa) were coordinately expressed in both preneoplassic and neoplastic nodules from both ciprofibrate and Solt-Farber hepatocarcinogenesis models.
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