Tetramer formation of tumor suppressor protein p53: Structure, function, and applications
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Updated: Mar 30, 2026

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
Rui Kamada1, Yu Toguchi1, Takao Nomura2
1Laboratory of Biological Chemistry, Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo, 060-0810, Japan.
Abstract:
Tetramer formation of p53 is essential for its tumor suppressor function. p53 not only acts as a tumor suppressor protein by inducing cell cycle arrest and apoptosis in response to genotoxic stress, but it also regulates other cellular processes, including autophagy, stem cell self-renewal, and reprogramming of differentiated cells into stem cells, immune system, and metastasis. More than 50% of human tumors have TP53 gene mutations, and most of them are missense mutations that presumably reduce tumor suppressor activity of p53. This review focuses on the role of the tetramerization (oligomerization), which is modulated by the protein concentration of p53, posttranslational modifications, and/or interactions with its binding proteins, in regulating the tumor suppressor function of p53. Functional control of p53 by stabilizing or inhibiting oligomer formation and its bio-applications are also discussed. © 2015 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 106: 598-612, 2016.
Insights
Tetramer formation of the p53 protein is crucial for its tumor suppressor activity. This review explores how p53 oligomerization, influenced by various factors, regulates its function and potential therapeutic applications.
Area of Science:
- Molecular Biology
- Biochemistry
- Cancer Research
Background:
- The p53 protein is a critical tumor suppressor involved in cell cycle arrest and apoptosis.
- Mutations in the TP53 gene are common in human cancers, often impairing p53's tumor suppressor function.
- p53 also regulates diverse cellular processes like autophagy, stem cell renewal, and metastasis.
Purpose of the Study:
- To review the essential role of p53 tetramerization in its tumor suppressor function.
- To discuss factors modulating p53 oligomerization, including protein concentration, posttranslational modifications, and binding proteins.
- To explore strategies for functional control of p53 via oligomer formation and its bio-applications.
Main Methods:
- Literature review focusing on p53 tetramerization and its functional implications.
- Analysis of how protein concentration, posttranslational modifications, and protein interactions affect p53 oligomerization.
- Discussion of methods to stabilize or inhibit p53 oligomer formation for therapeutic purposes.
Main Results:
- Tetramer formation is a key determinant of p53's tumor suppressor activity.
- p53 oligomerization is dynamically regulated by cellular conditions and molecular interactions.
- Dysregulation of p53 tetramerization is linked to its loss of function in cancer.
Conclusions:
- Modulating p53 tetramerization offers a potential strategy for cancer therapy.
- Understanding p53 oligomerization is vital for developing novel therapeutic interventions.
- Targeting p53 oligomerization could restore its tumor suppressor function in various cancers.
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