Wei Xiaolong, Xu Hai, Kufe Donald
Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
Cancer Cell. 2005 Feb;7(2):167-78. doi: 10.1016/j.ccr.2005.01.008.
The MUC1 oncoprotein is aberrantly overexpressed by most human carcinomas. The present work demonstrates that MUC1 associates with the p53 tumor suppressor, and that this interaction is increased by genotoxic stress. The MUC1 cytoplasmic domain binds directly to p53 regulatory domain. Chromatin immunoprecipitation assays demonstrate that MUC1 coprecipitates with p53 on the p53-responsive elements of the p21 gene promoter and coactivates p21 gene transcription. Conversely, MUC1 attenuates activation of Bax transcription. In concert with these results, MUC1 promotes selection of the p53-dependent growth arrest response and suppresses the p53-dependent apoptotic response to DNA damage. These findings indicate that MUC1 regulates p53-responsive genes and thereby cell fate in the genotoxic stress response.
大多数人类癌症中MUC1癌蛋白异常过表达。目前的研究表明,MUC1与p53肿瘤抑制因子相关联,并且这种相互作用在基因毒性应激下会增强。MUC1胞质结构域直接与p53调节结构域结合。染色质免疫沉淀分析表明,MUC1与p53在p21基因启动子的p53反应元件上共沉淀,并共同激活p21基因转录。相反,MUC1减弱Bax转录的激活。与这些结果一致,MUC1促进p53依赖的生长停滞反应的选择,并抑制p53依赖的对DNA损伤的凋亡反应。这些发现表明,MUC1调节p53反应基因,从而在基因毒性应激反应中决定细胞命运。