p73 tumor suppressor protein: a close relative of p53 not only in structure but also in anti-cancer approach?
Open accessAbstract
The discovery of the p53 tumor suppressor protein in 1979 shed new light on cancer cell biology and introduced a trend in cancer research focusing on p53-like proteins. This in turn led to the discovery of two homologous proteins of p53-p63 in 1998 and p73 in 1997. The p53 family members are mainly involved in apoptosis induction under cellular stress, but also in early embryonic developmental processes. The p63 and p73 proteins activate the transcription of a number of p53 target genes. The precise role of p63 in cancer cells is not fully revealed yet, unlike that of p53 and p73. The p53 tumor suppressor protein is found inactive in approximately 50% of human cancers. However, p73 is not as often inactivated in tumors. Of importance, transcriptionally active forms of p73 induce apoptosis in cancer cells independent of p53 status. Moreover, the regulatory mechanisms governing p73 stability in cells are well described. These features promoted the research concerning p73-targeted anti-cancer treatment. The p73 protein is subject to sophisticated activatory and inhibitory regulatory mechanisms. The up-to-date anti-cancer compounds targeting p73 protein in vitro inhibit its negative regulators, which leads to the activation of p73 pro-apoptotic function in cancer cells. In the current review we present the recent scientific findings on p73 regulation in cells and the newest anti-cancer strategies concerning its tumor suppressor function.
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p73α has functions similar to p53 but is regulated differently by Mdm2.
“The p53 family member p73α has functions similar to p53 (17, 18, 42, 43), but is regulated differently by Mdm2.”
From Potentiation of carboplatin-mediated DNA damage by the Mdm2 modulator Nutlin-3a in a humanized orthotopic breast-to-lung metastatic model (2015) · cites this paper as [42]
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- Authors
- Zawacka-Pankau, J., Kostecka, A., Sznarkowska, A., Hedström, E., & Kawiak, A.
- Venue
- Cell Cycle
- Publisher
- Informa UK Limited
- Published
- 2010-02-15
- Volume
- 9
- Issue
- 4
- Pages
- 720-728
- ISSN
- 1538-4101 (ISSN-L)
- 1551-4005
- OpenAlex
- W2075794624
- Cited by
- 67
- References
- 0
- Citations by year
- 2024: 2 · 2023: 1 · 2021: 1 · 2020: 3 · 2019: 3 · 2018: 4 · 2017: 3 · 2016: 2 · 2015: 5 · 2014: 8 · 2013: 11 · 2012: 10
- FWCI
- 5.53
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- Cell Cycle (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
- Keywords
- p73, p53 family, p63, tumor suppressor proteins, apoptosis, p53 target genes, embryonic development
- MeSH terms
- Tumor Protein p73, Antineoplastic Agents, DNA-Binding Proteins, Humans, Neoplasms, Nuclear Proteins, Photochemotherapy, Tumor Suppressor Protein p53, Apoptosis, Cyclin-Dependent Kinases, Tumor Suppressor Proteins
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