Editorials: Cell Cycle Features
Too much or too little: Harnessing senescence to control oncogene-driven cancer
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Volume 11, Issue 17 September 1, 2012
Pages 3147 - 3148
http://dx.doi.org/10.4161/cc.21588
Authors: Katherine M. Hannan and Richard B. Pearson
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- Katherine M. Hannan
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Oncogenic Signalling and Growth Control Program; Peter MacCallum Cancer Centre; Melbourne, VIC Australia; Sir Peter MacCallum Department of Oncology; The University of Melbourne; Parkville, VIC Australia
- Richard B. Pearson
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Corresponding author: rick.pearson@petermac.org
Oncogenic Signalling and Growth Control Program; Peter MacCallum Cancer Centre; Melbourne, VIC Australia; Sir Peter MacCallum Department of Oncology; The University of Melbourne; Parkville, VIC Australia; Department of Biochemistry and Molecular Biology; University of Melbourne; Parkville, VIC Australia
Abstract:
Comment on: Astle MV, et al. Oncogene 2012; 31:1949-62.
Editorials: Cell Cycle Features to:
MV Astle, KM Hannan, PY Ng, RS Lee, AJ George, AK Hsu, Y Haupt, RD Hannan, RB Pearson. AKT induces senescence in human cells via mTORC1 and p53 in the absence of DNA damage: implications for targeting mTOR during malignancy. Oncogene 2012; 31: 1949-62
PMID: 21909130 DOI: 10.1038/onc.2011.394
Received: June 20, 2012; Accepted: June 25, 2012; Published Online: August 16, 2012
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