Wirth P J, Benjamin T, Schwartz D M, Thorgeirsson S S
Cancer Res. 1986 Jan;46(1):400-13.
Using the Solt-Farber hepatocarcinogenesis model, a large population of preneoplastic and neoplastic nodules were induced in male Fischer 344 rats. Total cellular polypeptides from normal liver and individual preneoplastic and neoplastic nodules were analyzed for both qualitative and quantitative changes using computer assisted high resolution two-dimensional electrophoresis. Approximately 800-1000 cytosolic and 1200-1400 membrane associated polypeptides were readily separated and detected using an ultrasensitive silver stain. The polypeptide patterns were remarkably similar for each tissue and only four qualitative polypeptide differences were noted. One cytosolic polypeptide, 6.8/57 (designated pl/Mr X 10(-3), and three membrane associated polypeptides, 6.25/41, 6.75/24, and 6.05/21, were expressed in both preneoplastic and neoplastic nodules but not in normal liver. No qualitative polypeptide differences were detected among the individual preneoplastic or individual neoplastic nodules or between preneoplastic and neoplastic nodules. Numerous quantitative changes in both known markers for hepatocarcinogenesis and in as yet unidentified polypeptides were noted. In particular, the Ya subunit of glutathione S-transferase B, the Yb subunit of glutathione S-transferase A, as well as the three isoelectric point variants of the Yp subunit of glutathione S-transferase P were increased 2-, 4-, and 7-fold, respectively, in preneoplastic and neoplastic nodules. Whereas DT-diaphorase was increased 2-3-fold in hyperplastic nodules as compared to normal liver, no differences in the expression of albumin were noted. Although no differences were observed in the expression of aldehyde dehydrogenase in preneoplastic and neoplastic nodules, polypeptide b (6.9/54) was shifted slightly toward the basic region in normal liver. alpha-Fetoprotein was not detected in either preneoplastic or neoplastic nodules. In addition to these changes in known markers, comparison of 500-800 cytosolic and 750-1000 membrane associated polypeptides showed that roughly 4-10% of the polypeptides were undergoing quantitative changes of at least 4-fold during these stages of hepatocarcinogenesis. Thirty (10 cytosolic and 20 membrane) polypeptides were significantly down-regulated while 22 (7 cytosolic and 15 membrane) polypeptides were up-regulated in both preneoplastic and neoplastic nodules. In all cases the direction and magnitude of change were the same in both preneoplastic and neoplastic nodules with the exception of three polypeptides.(ABSTRACT TRUNCATED AT 400 WORDS)
利用索尔 - 法伯肝癌发生模型,在雄性费希尔344大鼠中诱导产生了大量癌前结节和肿瘤结节。使用计算机辅助高分辨率二维电泳分析正常肝脏以及各个癌前结节和肿瘤结节中的总细胞多肽,以检测其定性和定量变化。使用超灵敏银染法可轻松分离并检测出约800 - 1000种胞质多肽和1200 - 1400种膜相关多肽。每个组织的多肽图谱非常相似,仅发现四个定性多肽差异。一种胞质多肽,6.8/57(指定为pI/Mr×10⁻³),以及三种膜相关多肽,6.25/41、6.75/24和6.05/21,在癌前结节和肿瘤结节中均有表达,但在正常肝脏中未表达。在各个癌前结节或各个肿瘤结节之间,以及癌前结节和肿瘤结节之间未检测到定性多肽差异。在肝癌发生的这些阶段,观察到许多已知肝癌发生标志物以及尚未鉴定的多肽存在大量定量变化。特别是,谷胱甘肽S - 转移酶B的Ya亚基、谷胱甘肽S - 转移酶A的Yb亚基以及谷胱甘肽S - 转移酶P的Yp亚基的三种等电点变体在癌前结节和肿瘤结节中分别增加了2倍、4倍和7倍。与正常肝脏相比,增生性结节中的DT - 黄递酶增加了2 - 3倍,而白蛋白表达未发现差异。尽管在癌前结节和肿瘤结节中醛脱氢酶的表达未观察到差异,但多肽b(6.9/54)在正常肝脏中略微向碱性区域偏移。在癌前结节或肿瘤结节中均未检测到甲胎蛋白。除了这些已知标志物的变化外,对500 - 800种胞质多肽和750 - 1000种膜相关多肽的比较表明,在肝癌发生的这些阶段,约4 - 10%的多肽经历了至少4倍的定量变化。在癌前结节和肿瘤结节中,有30种(10种胞质和20种膜相关)多肽显著下调,22种(7种胞质和15种膜相关)多肽上调。除了三种多肽外,在所有情况下,癌前结节和肿瘤结节中的变化方向和幅度均相同。(摘要截于400字)