Authors:
A Chicas, X Wang, C Zhang, M McCurrach, Z Zhao, O Mert, RA Dickins, M Narita, M Zhang, SW Lowe
Journal name: 
Cancer Cell
Citation info: 
17(4):376-387
Abstract: 
The RB protein family (RB, p107, and p130) has overlapping and compensatory functions in cell-cycle control. However, cancer-associated mutations are almost exclusively found in RB, implying that RB has a nonredundant role in tumor suppression. We demonstrate that RB preferentially associates with E2F target genes involved in DNA replication and is uniquely required to repress these genes during senescence but not other growth states. Consequently, RB loss leads to inappropriate DNA synthesis following a senescence trigger and, together with disruption of a p21-mediated cell-cycle checkpoint, enables extensive proliferation and rampant genomic instability. Our results identify a nonredundant RB effector function that may contribute to tumor suppression and reveal how loss of RB and p53 cooperate to bypass senescence.
DOI: 
http://doi.org/10.1016/j.ccr.2010.01.023
Research group: 
Narita Group
E-pub date: 
13 Apr 2010