Polager Shirley, Ginsberg Doron
The Mina and Everard Goodman Faculty of Life Science, Bar Ilan University, Ramat Gan 52900, Israel.
Trends Cell Biol. 2008 Nov;18(11):528-35. doi: 10.1016/j.tcb.2008.08.003. Epub 2008 Sep 18.
The retinoblastoma tumor suppressor, pRb, restricts cell-cycle progression mainly by regulating members of the E2F-transcription-factor family. The Rb pathway is often inactivated in human tumors, resulting in deregulated-E2F activity that promotes proliferation or cell death, depending on the cellular context. Specifically, the outcome of deregulated-E2F activity is determined by integration of signals coming from the cellular DNA and the external environment. Alterations in cell proliferation and cell-death pathways are key features of transformed cells and, therefore, an understanding of the variables that determine the outcome of E2F activation is pivotal for cancer research and treatment. In this review, we discuss recent studies that have elucidated some of the signals affecting E2F activity and that have revealed additional E2F targets and functions, thereby enriching the understanding of this versatile transcription-factor family.
视网膜母细胞瘤肿瘤抑制因子pRb主要通过调节E2F转录因子家族成员来限制细胞周期进程。Rb通路在人类肿瘤中常常失活,导致E2F活性失调,这会促进细胞增殖或细胞死亡,具体取决于细胞环境。具体而言,E2F活性失调的结果由来自细胞DNA和外部环境的信号整合决定。细胞增殖和细胞死亡途径的改变是转化细胞的关键特征,因此,了解决定E2F激活结果的变量对于癌症研究和治疗至关重要。在本综述中,我们讨论了最近的研究,这些研究阐明了一些影响E2F活性的信号,并揭示了额外的E2F靶点和功能,从而丰富了对这个多功能转录因子家族的理解。