%0 Journal Article
%T Temporally distinct roles for tumor suppressor pathways in cell cycle arrest and cellular senescence in Cyclin D1-driven tumor
%A Hasan Zalzali
%A Mohammad Harajly
%A Lina Abdul-Latif
%A Nader El Chaar
%A Ghassan Dbaibo
%A Stephen X Skapek
%A Raya Saab
%J Molecular Cancer
%D 2012
%I BioMed Central
%R 10.1186/1476-4598-11-28
%X Senescence evolved over a period of weeks, with initial hyperproliferation followed by cell cycle arrest due to ROS production leading to activation of a DNA damage response and the p53 pathway. Interestingly, cell cycle exit was associated with repression of the Cyclin-dependent kinase Cdk2. This was followed days later by formation of heterochromatin foci correlating with RB protein hypophosphorylation. In the absence of the Cdk4-inhibitor p18Ink4c, cell cycle exit was delayed but most cells eventually showed a senescent phenotype. However, tumors later arose from this premalignant, largely senescent lesion. We found that the p53 pathway was intact in tumors arising in a p18Ink4c-/- background, indicating that the two genes represent distinct tumor suppressor pathways. Upon tumor progression, both p18Ink4c-/- and p53-/- tumors showed increased Cdk2 expression. Inhibition of Cdk2 in cultured pre-tumorigenic and tumor cells of both backgrounds resulted in decreased proliferation and evidence of senescence.Our findings indicate that the p53 and the RB pathways play temporally distinct roles in senescence induction in Cyclin D1-expressing cells, and that Cdk2 inhibition plays a role in tumor suppression, and may be a useful therapeutic target.
%K p18Ink4c
%K Cyclin D1
%K Senescence
%K p53
%K Rb
%K Cdk2
%K Tumor
%K Reactive oxygen species
%U http://www.molecular-cancer.com/content/11/1/28/abstract