Recommended Citation
Majumder M, House R, Palanisamy N, Qie S, Day TA, Neskey D, Diehl JA, and Palanisamy V. RNA-binding protein FXR1 regulates p21 and TERC RNA to bypass p53-mediated cellular senescence in OSCC. PLoS Genet 2016; 12(9):e1006306.
Document Type
Article
Publication Date
9-1-2016
Publication Title
PLoS Genet
Abstract
RNA-binding proteins (RBP) regulate numerous aspects of co- and post-transcriptional gene expression in cancer cells. Here, we demonstrate that RBP, fragile X-related protein 1 (FXR1), plays an essential role in cellular senescence by utilizing mRNA turnover pathway. We report that overexpressed FXR1 in head and neck squamous cell carcinoma targets (G-quadruplex (G4) RNA structure within) both mRNA encoding p21 (Cyclin-Dependent Kinase Inhibitor 1A (CDKN1A, Cip1) and the non-coding RNA Telomerase RNA Component (TERC), and regulates their turnover to avoid senescence. Silencing of FXR1 in cancer cells triggers the activation of Cyclin-Dependent Kinase Inhibitors, p53, increases DNA damage, and ultimately, cellular senescence. Overexpressed FXR1 binds and destabilizes p21 mRNA, subsequently reduces p21 protein expression in oral cancer cells. In addition, FXR1 also binds and stabilizes TERC RNA and suppresses the cellular senescence possibly through telomerase activity. Finally, we report that FXR1-regulated senescence is irreversible and FXR1-depleted cells fail to form colonies to re-enter cellular proliferation. Collectively, FXR1 displays a novel mechanism of controlling the expression of p21 through p53-dependent manner to bypass cellular senescence in oral cancer cells.
Medical Subject Headings
Carcinoma, Squamous Cell; Cell Line, Tumor; Cellular Senescence; Cyclin-Dependent Kinase Inhibitor p21; DNA Damage; Humans; Mouth Neoplasms; Protein Binding; RNA; RNA-Binding Proteins; Telomerase; Tumor Suppressor Protein p53
PubMed ID
27606879
Volume
12
Issue
9
First Page
e1006306
