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| Content Provider | Springer Nature Link |
|---|---|
| Author | Vilgelm, A. E. Zaika, A. I. Prassolov, V. S. |
| Copyright Year | 2011 |
| Abstract | For the first time, p53 was found in complex with the viral large T-antigen in cells transformed with the small DNA virus SV40. p53 cDNA was cloned in the early 1980s, and the full-length p53 gene was cloned soon afterwards. The p53 family is comprised of three genes—TP53, TP63, and TP73—each of which is expressed as a set of structurally and functionally different isoforms. All of them intensely interact with each other, forming a united functional network of proteins. The review discusses the evolution of the p53 family and the significance of all its members in embryo development, reproduction, regeneration, regulation of aging and lifespan, and defense against cancer. Special attention is paid to the role of poorly studied members of the p53 family, p63 and p73, in carcinogenesis and tumor progression. Different isoforms of these proteins might exert opposite effects on these processes. |
| Starting Page | 156 |
| Ending Page | 171 |
| Page Count | 16 |
| File Format | |
| ISSN | 00268933 |
| Journal | Molecular Biology |
| Volume Number | 45 |
| Issue Number | 1 |
| e-ISSN | 16083245 |
| Language | English |
| Publisher | SP MAIK Nauka/Interperiodica |
| Publisher Date | 2011-02-22 |
| Publisher Place | Dordrecht |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | tumor suppressors p53 p63 p73 genetic stability apoptosis carcinogenesis aging cell growth regulation Human Genetics Biochemistry Life Sciences |
| Content Type | Text |
| Resource Type | Article |
| Subject | Structural Biology Biophysics |
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