Nakano H, Hatayama I, Satoh K, Suzuki S, Sato K, Tsuchida S
Second Department of Biochemistry, Hirosaki University School of Medicine, Japan.
Carcinogenesis. 1994 Sep;15(9):1853-7. doi: 10.1093/carcin/15.9.1853.
Expression of the oncogene product c-Jun was examined and compared with that of class pi glutathione S-transferase (GST-II) during chemical hepatocarcinogenesis in female and male mice. A single i.p. injection of diethylnitrosamine (DEN) (10 mg/kg) was administered to B6C3F1 mice and livers were immunohistochemically investigated with anti-c-Jun and anti-GST-II antibodies at various time points thereafter. In females, almost all foci detected by hematoxylin and eosin staining were positive for c-Jun 3, 6, 9 and 11 months after the DEN administration. Seventy-one and 82% of c-Jun-positive foci at 9 and 11 months respectively, were also positive for GST-II, while this was the case for only 15% at 6 months. In males almost all foci were also positive for c-Jun at 3 and 6 months, but 23% of foci were negative at 9 months. Unlike the foci in females, 96 and 79% of those in males expressing c-Jun were negative for GST-II at 6 and 9 months respectively. Both GST-II expression in foci of females and its lack in those of males were highly correlated with c-Jun expression. Furthermore, single cells expressing c-Jun were also observed in both sexes at 3 months and thereafter, but not at 2 or 4 weeks. Alterations in the numbers of c-Jun-positive single cells, minifoci and foci followed sequentially revealed the number of such single cells to decrease, while foci increased, the sum being relatively constant. On the other hand, while a large number of GST-II-positive single cells were detected in female livers 2 and 4 weeks after the DEN administration, they markedly decreased thereafter, suggesting that the majority were unlikely to give rise to foci. Thus, c-Jun may be a better positive marker not only for preneoplastic foci, but also putative precursor single cells in both female and male mice and therefore be useful for analysis of hepatocarcinogenic processes.
在雌性和雄性小鼠化学性肝癌发生过程中,对癌基因产物c-Jun的表达进行了检测,并与π类谷胱甘肽S-转移酶(GST-II)的表达进行了比较。给B6C3F1小鼠腹腔注射一次二乙基亚硝胺(DEN)(10 mg/kg),此后在不同时间点用抗c-Jun和抗GST-II抗体对肝脏进行免疫组织化学研究。在雌性小鼠中,苏木精和伊红染色检测到的几乎所有病灶在给予DEN后3、6、9和11个月时c-Jun呈阳性。在9个月和11个月时,分别有71%和82%的c-Jun阳性病灶GST-II也呈阳性,而在6个月时只有15%的病灶如此。在雄性小鼠中,几乎所有病灶在3个月和6个月时c-Jun也呈阳性,但在9个月时有23%的病灶呈阴性。与雌性小鼠的病灶不同,雄性小鼠中表达c-Jun的病灶在6个月和9个月时分别有96%和79%的GST-II呈阴性。雌性小鼠病灶中GST-II的表达及其在雄性小鼠病灶中的缺失均与c-Jun的表达高度相关。此外,在3个月及之后,在两性中均观察到表达c-Jun的单个细胞,但在2周或4周时未观察到。c-Jun阳性单个细胞、微小病灶和病灶数量的变化依次显示,此类单个细胞数量减少,而病灶数量增加,总数相对恒定。另一方面,在给予DEN后2周和4周,在雌性小鼠肝脏中检测到大量GST-II阳性单个细胞,但此后它们明显减少,这表明大多数此类细胞不太可能形成病灶。因此,c-Jun不仅可能是肿瘤前病灶的更好阳性标志物,也是雌性和雄性小鼠中假定的前体单个细胞的更好阳性标志物,因此可用于分析肝癌发生过程。