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Updated: Jun 25, 2026

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
Antimutagenic efficacy of some natural compounds on cyclophosphamide-induced p53 alterations
Eman M Gouda1, Adel M Elbehairy, Magdy A Ghoneim
1Biochemistry Department and Biotechnology Center, Faculty of Veterinary Medicine, Cairo University, 12211 Giza, Egypt. emanmgouda@hotmail.com
Abstract:
Mutations in the p53 tumour suppressor gene have been associated with chemical carcinogens. Natural antimutagens are promising modulators for reducing the cancer risk. The present study was carried out to assess the protective efficacy of some natural antimutagens against p53 alterations. We investigated the ability of curcumin (100 mg/kg BW) and chlorophyllin (3 mg/kg BW) pretreatment, for three times per week for three successive weeks, to inhibit mutations induced by intraperitoneal injection of a single dose of 40 mg/kg BW of cyclophosphamide (CP). Forty male albino rats were assigned into four groups: control nontreated group, CP-treated group, curcumin-CP-treated group, and chlorophyllin-CP-treated group. Liver samples were collected for DNA isolation two days after CP injection. The isolated DNA was used in single-strand conformational polymorphism (SSCP) analysis of polymerase chain reaction (PCR)-amplified products of four regions: two in exon 5, one in exon 6, and one in exon 7. The amplified products of p53 different regions were found to be in the expected molecular size of the designed primers. SSCP analysis of these amplified products showed that CP-induced mutation in the p53 gene was found only in exon 7 shifting its electrophoretic mobility. Chlorophyllin treatment prior to CP injection had a more potent protective efficacy (80%) than that with curcumin (33.3%).
Insights
Natural antimutagens like chlorophyllin and curcumin show promise in preventing p53 gene mutations caused by the chemical carcinogen cyclophosphamide (CP). Chlorophyllin demonstrated a higher protective efficacy against these p53 alterations.
Area of Science:
- Biochemistry
- Molecular Biology
- Toxicology
Background:
- Mutations in the p53 tumor suppressor gene are linked to chemical carcinogens.
- Natural antimutagens offer potential strategies for cancer risk reduction.
- Assessing natural compounds' efficacy against p53 alterations is crucial for cancer prevention.
Purpose of the Study:
- To evaluate the protective effects of curcumin and chlorophyllin against p53 gene mutations induced by cyclophosphamide (CP).
- To investigate the modulation of p53 alterations by natural antimutagens in a rat model.
Main Methods:
- Rats were pretreated with curcumin or chlorophyllin before CP injection.
- DNA was isolated from liver samples for analysis.
- Single-strand conformational polymorphism (SSCP) analysis was performed on PCR-amplified p53 gene regions (exons 5, 6, and 7).
Main Results:
- Cyclophosphamide (CP) induced a mutation in exon 7 of the p53 gene, indicated by a shift in electrophoretic mobility.
- Chlorophyllin pretreatment exhibited a significant protective efficacy of 80% against CP-induced p53 mutations.
- Curcumin pretreatment showed a lower protective efficacy of 33.3%.
Conclusions:
- Chlorophyllin is a potent natural antimutagen effective in preventing cyclophosphamide-induced p53 gene mutations.
- Curcumin also offers some protection but to a lesser extent than chlorophyllin.
- These findings support the potential of natural antimutagens in chemoprevention strategies against carcinogen-induced DNA damage.
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