| Literature DB >> 15729694 |
Rachel G Berkson1, Jonathan J Hollick, Nicholas J Westwood, Julie A Woods, David P Lane, Sonia Lain.
Abstract
Activation of the p53 tumour suppressor is predicted to have therapeutically beneficial effects. Many current anti-cancer therapies activate the p53 response via DNA damage. Non-genotoxic activation of the p53 pathway would open the way to long-term and possibly prophylactic treatments. We have established a simple protocol to screen small compound libraries for activators of p53-dependent transcription, and to select and characterise the most interesting hits, which include non-genotoxic activators. These compounds or their derivatives are of potential clinical interest. This approach may also lead to the identification of novel p53-activating compound families and possibly to the description of novel molecular pathways regulating p53 activity. (c) 2005 Wiley-Liss, Inc.Entities:
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Year: 2005 PMID: 15729694 DOI: 10.1002/ijc.20968
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396