Summaryp63 and p73 are functionally and structurally related to the tumor suppressor p53. However, their own role in tumor suppression is unclear. Given the p53-like properties of p63 and p73, we tested whether they are involved in tumor suppression by aging mice heterozygous for mutations in all p53 family genes and scored for spontaneous tumors. We show here that p63+/−;p73+/− mice develop spontaneous tumors. Loss of p63 and p73 can also cooperate with loss of p53 in tumor development. Mice heterozygous for mutations in both p53 and p63 or p53 and p73 displayed higher tumor burden and metastasis compared to p53+/− mice. These findings provide evidence for a broader role for the p53 family than has been previously reported
AbstractTP53 belongs to a small gene family that includes, in mammals, two additional paralogs, TP63...
p73 is a tumor suppressor belonging to the p53 family of transcription factors. Distinct isoforms ar...
The p53 gene is the most frequently mutated gene in human cancer. The identification of two homologu...
Homology between p63 and p53 has suggested that these proteins might function similarly. However, th...
The p53 tumor suppressor gene is the most frequent target for genetic alterations in human cancers, ...
p73 and p63 are two homologs of the tumor suppressive transcription factor p53. Given the high degre...
AbstractWhile p53 family members have distinct nonoverlapping functions, the involvement of p63 and ...
p53 is the most frequently inactivated tumor suppressor gene in human cancer, whereas its homologue,...
p73 (ref. 1) has high homology with the tumour suppressor p53 (refs 2-4), as well as with p63, a gen...
Many cancers express mutant p53 proteins that have lost wild-type tumor suppressor activity and, in ...
Mutations in the TP53 gene commonly result in the expression of a full-length protein that drives ca...
p53, the original member of the family of genes now known to include p63 and p73, was first heralded...
The transcription factor and tumour suppressor p53 and its two homologues p63 and p73 form a family ...
p63, a member of the p53 gene family, known to play a role in development, has more recently also be...
International audienceThe p53 protein is related by sequence homology and function to the products o...
AbstractTP53 belongs to a small gene family that includes, in mammals, two additional paralogs, TP63...
p73 is a tumor suppressor belonging to the p53 family of transcription factors. Distinct isoforms ar...
The p53 gene is the most frequently mutated gene in human cancer. The identification of two homologu...
Homology between p63 and p53 has suggested that these proteins might function similarly. However, th...
The p53 tumor suppressor gene is the most frequent target for genetic alterations in human cancers, ...
p73 and p63 are two homologs of the tumor suppressive transcription factor p53. Given the high degre...
AbstractWhile p53 family members have distinct nonoverlapping functions, the involvement of p63 and ...
p53 is the most frequently inactivated tumor suppressor gene in human cancer, whereas its homologue,...
p73 (ref. 1) has high homology with the tumour suppressor p53 (refs 2-4), as well as with p63, a gen...
Many cancers express mutant p53 proteins that have lost wild-type tumor suppressor activity and, in ...
Mutations in the TP53 gene commonly result in the expression of a full-length protein that drives ca...
p53, the original member of the family of genes now known to include p63 and p73, was first heralded...
The transcription factor and tumour suppressor p53 and its two homologues p63 and p73 form a family ...
p63, a member of the p53 gene family, known to play a role in development, has more recently also be...
International audienceThe p53 protein is related by sequence homology and function to the products o...
AbstractTP53 belongs to a small gene family that includes, in mammals, two additional paralogs, TP63...
p73 is a tumor suppressor belonging to the p53 family of transcription factors. Distinct isoforms ar...
The p53 gene is the most frequently mutated gene in human cancer. The identification of two homologu...