More targets, more pathways and more clues for mutant p53

• Published in: Oncogenesis (New York, NY) Vol. 2; no. 7; p. e54
• Main Authors: Garritano, S, Inga, A, Gemignani, F, Landi, S
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01-07-2013; Nature Publishing Group
• Subjects: 631/208/737; 631/67/2327; 631/67/581; Apoptosis; Cell Biology; Human Genetics; Internal Medicine; Medicine; Medicine & Public Health; Oncology; Review; target genes; microarray; p53
• ISSN: 2157-9024; 2157-9024
• DOI: 10.1038/oncsis.2013.15

Mutations in the transcription factor p53 are among the most common genetic alterations in human cancer, and missense p53 mutations in cancer cells can lead to aggressive phenotypes. So far, only few studies investigated transcriptional reprogramming under mutant p53 expression as a means to identify deregulated targets and pathways. A review of the literature was carried out focusing on mutant p53-dependent transcriptome changes with the aims of (i) verifying whether different p53 mutations can be equivalent for their effects, or whether there is a mutation-specific transcriptional reprogramming of target genes, (ii) understanding what is the main mechanism at the basis of upregulation or downregulation of gene expression under the p53 mutant background, (iii) identifying novel candidate target genes of WT and/or mutant p53 and (iv) defining cellular pathways affected by the mutant p53-dependent gene expression reprogramming. Nearly 600 genes were consistently found upregulated or downregulated upon ectopic expression of mutant p53, regardless of the specific p53 mutation studied. Promoter analysis and the use of ChIP-seq data indicate that, for most genes, the expression changes could be ascribed to a loss both of WT p53 transcriptional activation and repressor functions. Pathway analysis indicated changes in the metabolism/catabolism of amino acids such as aspartate, glutamate, arginine and proline. Novel p53 candidate target genes were also identified, including
ARID3B
,
ARNT2
,
CLMN
,
FADS1
,
FTH1
,
KPNA2
,
LPHN2
,
PARD6B
,
PDE4C
,
PIAS2
,
PRPF40A
,
PYGL
and
RHOBTB2
, involved in the metabolism, xenobiotic responses and cell differentiation.