Related Experiment Video
Updated: Aug 4, 2025

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
Diverse rescue potencies of p53 mutations to ATO are predetermined by intrinsic mutational properties
Huaxin Song1, Jiale Wu1, Yigang Tang1
1Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Abstract:
Tumor suppressor p53 is inactivated by thousands of heterogeneous mutations in cancer, but their individual druggability remains largely elusive. Here, we evaluated 800 common p53 mutants for their rescue potencies by the representative generic rescue compound arsenic trioxide (ATO) in terms of transactivation activity, cell growth inhibition, and mouse tumor-suppressive activities. The rescue potencies were mainly determined by the solvent accessibility of the mutated residue, a key factor determining whether a mutation is a structural one, and the temperature sensitivity, the ability to reassemble the wild-type DNA binding surface at a low temperature, of the mutant protein. A total of 390 p53 mutants were rescued to varying degrees and thus were termed as type 1, type 2a, and type 2b mutations, depending on the degree to which they were rescued. The 33 type 1 mutations were rescued to amounts comparable to the wild type. In PDX mouse trials, ATO preferentially inhibited growth of tumors harboring type 1 and type 2a mutants. In an ATO clinical trial, we report the first-in-human mutant p53 reactivation in a patient harboring the type 1 V272M mutant. In 47 cell lines derived from 10 cancer types, ATO preferentially and effectively rescued type 1 and type 2a mutants, supporting the broad applicability of ATO in rescuing mutant p53. Our study provides the scientific and clinical communities with a resource of the druggabilities of numerous p53 mutations (www.rescuep53.net) and proposes a conceptual p53-targeting strategy based on individual mutant alleles rather than mutation type.
Insights
Arsenic trioxide (ATO) rescues numerous mutated tumor suppressor p53 proteins, with rescue effectiveness linked to mutation type and protein structure. This study identifies druggable p53 mutants and demonstrates clinical potential.
Area of Science:
- Oncology
- Molecular Biology
- Drug Discovery
Background:
- The tumor suppressor p53 is frequently mutated in cancer, leading to diverse mutations that complicate targeted therapies.
- Understanding the druggability of individual p53 mutants is crucial for developing effective cancer treatments.
Purpose of the Study:
- To evaluate the rescue potency of arsenic trioxide (ATO) across 800 common p53 mutants.
- To identify factors influencing p53 mutant rescue and assess ATO's therapeutic potential in preclinical and clinical settings.
Main Methods:
- Assessed p53 mutant rescue by ATO based on transactivation activity, cell growth inhibition, and tumor suppression in mice.
- Analyzed rescue potency in relation to solvent accessibility and temperature sensitivity of p53 mutants.
- Conducted patient-derived xenograft (PDX) mouse trials and a first-in-human clinical trial with ATO.
Main Results:
- 390 p53 mutants showed varying degrees of rescue by ATO, categorized into type 1, 2a, and 2b.
- Type 1 mutations (33 identified) were rescued to wild-type levels.
- ATO preferentially inhibited tumor growth in mice with type 1 and type 2a mutants and showed clinical efficacy in a patient with a type 1 V272M mutant.
Conclusions:
- ATO demonstrates broad applicability in rescuing various p53 mutants, particularly type 1 and 2a.
- Rescue potency is predictable based on mutation characteristics like solvent accessibility and temperature sensitivity.
- This research provides a valuable resource for p53 mutation druggability and supports allele-specific therapeutic strategies.
More Related Videos
09:32Procedure and Key Optimization Strategies for an Automated Capillary Electrophoretic-based Immunoassay Method
Published on: September 10, 2017
06:38High Sensitivity Measurement of Transcription Factor-DNA Binding Affinities by Competitive Titration Using Fluorescence Microscopy
Published on: February 7, 2019
Related Concept Videos
Abnormal Proliferation
DNA Damage can Stall the Cell Cycle
Spontaneous and Induced Mutations
Mutagenicity and Carcinogenicity
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Negative Regulator Molecules