Duan Wenrui, Gao Li, Druhan Lawrence J, Zhu Wei-Guo, Morrison Carl, Otterson Gregory A, Villalona-Calero Miguel A
Comprehensive Cancer Center and Department of Internal Medicine, The Ohio State University College of Medicine and Public Health, Columbus 43210-1240, USA.
J Natl Cancer Inst. 2004 Nov 17;96(22):1718-21. doi: 10.1093/jnci/djh292.
Maintenance of p53 function is important for normal cell growth and development, and loss of p53 function contributes directly to malignant tumor development. The recently discovered Pirh2 protein is an ubiquitin-protein ligase that negatively regulates p53 through activity by targeting it for degradation. To determine how Pirh2 may mediate lung tumorigenesis, we evaluated Pirh2 expression in human and mouse lung tumor samples and paired normal lung tissues using immunoblot analysis and immunohistochemistry. Pirh2 protein expression was higher in 27 (84%) of 32 human lung neoplasms than in matched normal lung tissue and in 14 of 15 mouse lung tumors evaluated. In addition, p53 protein was more ubiquitinated in the mouse lung tumors than in normal tissue, and overall p53 expression was lower than that in normal tissue. These results are consistent with the hypothesis that increased Pirh2 expression affects lung tumorigenesis by reducing p53 activity. To our knowledge, this is the first description of altered Pirh2 expression in human and mouse tumors.
维持p53功能对于正常细胞生长和发育至关重要,而p53功能丧失直接促成恶性肿瘤的发展。最近发现的Pirh2蛋白是一种泛素蛋白连接酶,通过将p53靶向降解来负向调节其活性。为了确定Pirh2如何介导肺癌发生,我们使用免疫印迹分析和免疫组织化学评估了Pirh2在人及小鼠肺肿瘤样本和配对正常肺组织中的表达。在32例人类肺肿瘤中的27例(84%)中,Pirh2蛋白表达高于配对的正常肺组织,在评估的15例小鼠肺肿瘤中的14例中也是如此。此外,与正常组织相比,小鼠肺肿瘤中的p53蛋白泛素化程度更高,且总体p53表达低于正常组织。这些结果与以下假设一致,即Pirh2表达增加通过降低p53活性影响肺癌发生。据我们所知,这是首次描述人类和小鼠肿瘤中Pirh2表达的改变。