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- Title
- Structure and apoptotic function of p73
- Author(s)
- Mi Kyung Yoon; Ji Hyang Ha; Min Sung Lee; Seung-Wook Chi
- Bibliographic Citation
- BMB Reports, vol. 48, no. 2, pp. 81-90
- Publication Year
- 2015
- Abstract
- p73 is a structural and functional homologue of the p53 tumor suppressor protein. Like p53, p73 induces apoptosis and cell cycle arrest and transactivates p53-responsive genes, conferring its tumor suppressive activity. In addition, p73 has unique roles in neuronal development and differentiation. The importance of p73-induced apoptosis lies in its capability to substitute the pro-apoptotic activity of p53 in various human cancer cells in which p53 is mutated or inactive. Despite the great importance of p73-induced apoptosis in cancer therapy, little is known about the molecular basis of p73-induced apoptosis. In this review, we discuss the p73 structures reported to date, detailed structural comparisons between p73 and p53, and current understanding of the transcription-dependent and -independent mechanisms of p73-induced apoptosis.
- Keyword
- ApoptosisCancer therapyp53 protein familyp73Structure
- ISSN
- 1225-8687
- Publisher
- Korea Soc-Assoc-Inst
- Full Text Link
- http://dx.doi.org/10.5483/BMBRep.2015.48.2.255
- Type
- Article
- Appears in Collections:
- Division of A.I. & Biomedical Research > 1. Journal Articles
- Files in This Item:
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