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Updated: Jul 14, 2026

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
[wt-p53 gene repair for p53 mutations of salivary pleomorphic adenoma cells]
Xu Wang1, Jie Wang, Fu-sheng Dong
1Department of Oral Pathology, College of Stomatology, Hebei Medical University, Shijiazhuang 050017, China.
Objective:
To analyze the original mutated codon of p53 gene of salivary pleomorphic adenoma (SPA) and to evaluate the repair effects of wt-p53 on SPA cells.
Methods:
Four cases of SPA were obtained from clinical fresh samples and SPA cells were separated and cultured, and then the cells were transduced by Ad-wt-p53. The cells and the corresponding tumor tissue DNA were extracted, PCR and single strand conformational polymorphism (SSCP) and DNA sequencing analysis were performed.
Results:
PCR-SSCP analysis showed 3 out of 4 SPA with abnormal exon 8 and abnormal exon 6. DNA sequencing analysis showed that exon 6 point mutation was found at codon 203 (GTG-->GCG), poly-codon mutations were found in exon 8 at codon 272 (GTG-->GT square), 275 (TGT-->T square T), 276 (GCC--> square CC) and at codon 290 (CGC-->CGCC). After transduced by Ad-wt-p53, all of the mutated codons were repaired.
Conclusions:
p53 gene mutation involved many codons that occurred frequently in the tumorigenesis of SPA. Exogenous wt-p53 could compensate and repair all the mutated p53 codons of SPA cells. SPA cells transduced by Ad-wt-p53 showed the typical apoptosis.
Insights
p53 gene mutations are common in salivary pleomorphic adenoma (SPA). Introducing wild-type p53 (wt-p53) successfully repaired these mutations and induced apoptosis in SPA cells.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Context:
- Salivary pleomorphic adenoma (SPA) is a common salivary gland tumor.
- The p53 tumor suppressor gene plays a critical role in cancer development.
- Understanding p53 mutations in SPA is crucial for therapeutic strategies.
Purpose:
- To identify specific p53 gene mutations in SPA.
- To assess the efficacy of wild-type p53 (wt-p53) gene therapy in repairing these mutations.
- To investigate the effect of wt-p53 on SPA cell apoptosis.
Summary:
- Analysis of four SPA cases revealed mutations in exons 6 and 8 of the p53 gene.
- Specific mutations identified include point mutations at codon 203 and multiple codon mutations in exon 8.
- Transduction with Ad-wt-p53 effectively repaired all identified p53 mutations in SPA cells.
- SPA cells treated with Ad-wt-p53 exhibited characteristic apoptosis.
Impact:
- This study demonstrates that p53 gene mutations are frequent in SPA tumorigenesis.
- Exogenous wt-p53 can effectively compensate for and repair mutated p53 codons in SPA cells.
- The findings suggest a potential therapeutic strategy for SPA using wt-p53 gene delivery to induce apoptosis.
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