Sabourin C L, Wang Q S, Ralston S L, Evans J, Coate J, Herzog C R, Jones S L, Weghorst C M, Kelloff G J, Lubet R A, You M, Stoner G D
Division of Environmental Health Sciences, School of Public Health, Ohio State University, Columbus, USA.
Exp Lung Res. 1998 Jul-Aug;24(4):499-521. doi: 10.3109/01902149809087383.
Cyclin D1 dysregulation and differential inactivation of p16INK4a and Rb have been observed in human lung cancer. In chemically induced mouse lung tumors, the p16INK4a gene is a target of inactivation, and Rb is reduced at the mRNA level (Northern blot) although similar at the protein level (Western blot) when compared to normal lung tissues. The expression of cyclin D1, cdk4, p16INK4a, and Rb protein was examined by immunohistochemistry in 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced mouse lung tumors. Immunohistochemical staining revealed exclusive nuclear staining of both cyclin D1 and cdk4 that was light to moderate in normal mouse lung tissues, but intense in lung adenomas and adenocarcinomas. Western blot analysis confirmed the increased expression of cyclin D1 and cdk4 in lung tumors compared to normal lung. Immunohistochemical analyses of lung tumors showed focal areas which lacked p16INK4a staining. Expression of p16INK4a, as determined by RT-PCR, was variable in lung tumors. Mutations in p16INK4a were not found by SSCP analysis. Immunohistochemical analyses of normal lung tissues showed intense staining for Rb protein in alveolar epithelial cells and in other lung cell types; however, in the lung tumors the staining intensity was reduced and the distribution was altered. Expression of Rb was detected in normal lung tissues but was barely detectable by Northern blot hybridization in lung tumors. Western blot analysis indicated the presence of both hypophosphorylated and hyperphosphorylated Rb protein in lung tumors and in normal lung tissues. These results suggest that alterations in the cell cycle proteins, cyclin D1, cdk4, p16INK4a, and Rb, may play a role in the acquisition of autonomous growth by adenomas. Furthermore, they demonstrate the importance of immunohistochemical studies to examine expression in tissues that contain multiple cell types, such as the lung, and in tumors that by nature are heterogeneous.
在人类肺癌中已观察到细胞周期蛋白D1失调以及p16INK4a和Rb的差异性失活。在化学诱导的小鼠肺肿瘤中,p16INK4a基因是失活的靶点,与正常肺组织相比,Rb在mRNA水平降低(Northern印迹法),尽管在蛋白质水平相似(Western印迹法)。通过免疫组织化学检测了4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮(NNK)诱导的小鼠肺肿瘤中细胞周期蛋白D1、细胞周期蛋白依赖性激酶4(cdk4)、p16INK4a和Rb蛋白的表达。免疫组织化学染色显示细胞周期蛋白D1和cdk4均为细胞核染色,在正常小鼠肺组织中为轻度至中度,但在肺腺瘤和腺癌中强烈。Western印迹分析证实与正常肺相比,肺肿瘤中细胞周期蛋白D1和cdk4的表达增加。肺肿瘤的免疫组织化学分析显示存在缺乏p16INK4a染色的局灶区域。通过逆转录聚合酶链反应(RT-PCR)测定,肺肿瘤中p16INK4a的表达是可变的。单链构象多态性(SSCP)分析未发现p16INK4a的突变。正常肺组织的免疫组织化学分析显示肺泡上皮细胞和其他肺细胞类型中Rb蛋白染色强烈;然而,在肺肿瘤中,染色强度降低且分布改变。在正常肺组织中检测到Rb的表达,但在肺肿瘤中通过Northern印迹杂交几乎检测不到。Western印迹分析表明肺肿瘤和正常肺组织中均存在低磷酸化和高磷酸化的Rb蛋白。这些结果表明细胞周期蛋白D1、cdk4、p16INK4a和Rb等细胞周期蛋白的改变可能在腺瘤自主生长的获得中起作用。此外,它们证明了免疫组织化学研究在检查包含多种细胞类型的组织(如肺)以及本质上异质性的肿瘤中的表达的重要性。