p53 family isoforms

被引:54
作者
Bourdon, Jean-Christophe [1 ,2 ]
机构
[1] Univ Dundee, Ninewells Hosp, Dept Surg, CR UK Cell Transformat Res Grp, Dundee DD1 4HN, Scotland
[2] Univ Dundee, Ninewells Hosp, Dept Mol Oncol, Dundee DD1 4HN, Scotland
关键词
splice; promoter; tumour; transcription; apoptosis; mutation; cell cycle;
D O I
10.2174/138920107783018444
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p63, p73 and p53 are transcription factors members of the p53 gene family involved in development, differentiation and cell response to stress. p53 gene is mutated in 50% of human cancer. Moreover, when p53 gene is not mutated then its tumour suppressor pathway is lost through interaction with abnormally expressed cellular protein or viral protein. Therefore p53 pathway inactivation is a common denominator to cancer. However, it is still difficult to associate in the clinic p53 status to cancer prognosis and diagnosis. Recent publications may have a profound impact on our understanding of p53 tumour suppressor activity. p63, p73 and p53 genes have a dual gene structure conserved in drosophila, zebrafish and man. They encode for multiple p63, p73 or p53 proteins containing different protein domains (isoforms) due to multiple splicing, alternative promoter and alternative initiation of translation. The interplay between p53, p63 and p73 isoforms are likely to be fundamental to our understanding of tumour formation.
引用
收藏
页码:332 / 336
页数:5
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