Title of article
Targeting p73 in cancer
Author/Authors
Maas ، نويسنده , , Anna-Maria and Bretz، نويسنده , , Anne Catherine and Mack، نويسنده , , Elisabeth and Stiewe، نويسنده , , Thorsten، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2013
Pages
8
From page
229
To page
236
Abstract
p73 is a member of the p53 family of tumor suppressors. Transactivating isoforms of p73 (TAp73) have p53-like, anti-proliferative and pro-apoptotic activities that are crucial for an efficient chemotherapy response. In line with this, genetic studies in mice have confirmed that TAp73 acts as a tumor suppressor. However, in contrast to p53, which is commonly inactivated in human cancer by point mutations, the TP73 gene is almost never mutated. Instead, the tumor suppressor activity of TAp73 is inhibited through a variety of mechanisms including epigenetic silencing and complex formation with inhibitory proteins. All these mechanisms have in common that they are in principle reversible and therefore amenable to therapeutic intervention. Here, we will review how tumor cells control the tumor suppressor activity of TAp73 and discuss possible strategies targeting p73 for reactivation.
Keywords
p53 , Molecular therapy , Tumor Suppressor Genes , p73
Journal title
Cancer Letters
Serial Year
2013
Journal title
Cancer Letters
Record number
1822635
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