Niwa S, Ueno S, Shirasu R
Graduate School of Dentistry, First Department of Oral and Maxillofacial Surgery, Osaka Dental University, 8-1 Kuzuhahanazono-cho, Hirakata-shi Osaka 573-1121, Japan.
Oral Oncol. 2001 Oct;37(7):579-85. doi: 10.1016/s1368-8375(00)00141-x.
We investigated the immunohistochemical expression of Rb protein (pRb), which plays an important role in the regulation of the cell cycle, in rat tongue carcinoma induced by 4-nitroquinoline 1-oxide. In addition, we made an immunohistochemical investigation of cyclin D1 and cdk4, which are involved in the Rb pathway. The labeling index of pRb expression in cases with carcinoma was significantly decreased compared with that in cases with a premalignant lesion (P<0.01), while the labeling index of cyclin D1 and cdk4 increased gradually during the course of carcinogenesis. We analyzed the phosphorylation of pRb by immunoblotting using G3-245 monoclonal antibody, which recognizes both the phosphorylated and unphosphorylated forms of pRb. Although expression of the phosphorylated pRb band was notably increased in dysplastic membrane compared with the control membrane, it almost disappeared in cases with carcinoma. Unphosphorylated pRb bands were also expressed in control membrane and dysplastic membrane but not in cases with carcinoma. In conclusion, a decrease of pRb and an increase of cdk4 and cyclin D1 were shown to occur during the premalignant stage. The decrease of pRb in quantity and the increase of its phosphorylation may prevent G1 arrest and consequently accelerate proliferation of the chemically injured cells contributing to the initiation of carcinogenesis.
我们研究了在4-硝基喹啉-1-氧化物诱导的大鼠舌癌中,对细胞周期调控起重要作用的Rb蛋白(pRb)的免疫组化表达。此外,我们还对参与Rb通路的细胞周期蛋白D1和细胞周期蛋白依赖性激酶4进行了免疫组化研究。癌组织中pRb表达的标记指数与癌前病变组织相比显著降低(P<0.01),而细胞周期蛋白D1和细胞周期蛋白依赖性激酶4的标记指数在致癌过程中逐渐升高。我们使用能识别pRb磷酸化和非磷酸化形式的G3-245单克隆抗体,通过免疫印迹分析pRb的磷酸化情况。虽然与对照膜相比,发育异常膜中磷酸化pRb条带的表达明显增加,但在癌组织中几乎消失。非磷酸化pRb条带在对照膜和发育异常膜中也有表达,但在癌组织中未表达。总之,在癌前阶段显示出pRb减少,细胞周期蛋白依赖性激酶4和细胞周期蛋白D1增加。pRb数量的减少及其磷酸化的增加可能会阻止G1期停滞,从而加速化学损伤细胞的增殖,促进致癌作用的起始。