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Updated: Aug 20, 2025

Identifying DNA Mutations in Purified Hematopoietic Stem/Progenitor Cells
Published on: February 24, 2014
Genotoxicity, DNA damage and sperm defects induced by vinblastine
Maha A Fahmy1, Entesar E Hassan2, Ayman A Farghaly1
1Department of Genetics and Cytology, National Research Centre (NRC), Dokki, Giza, Egypt.
Background:
The treatment with chemotherapy may develop secondary tumors as a result of chemo genotoxicity. Sperm defects is another complication associated with chemo treatment. In this study the genotoxicity of vinblastine (VB) was estimated in both somatic and germ cells.
Materials:
85 mice were taken. Four single doses of VB at 3, 4.5, 6 and 10 mg/kg and three successive doses at 3, 4.5 and 6 mg/kg were taken for estimation of chromosomal aberrations (CAs). Four single doses of VB were involved in estimating the DNA fragmentation, and comet assay. For sperm abnormalities mice were injected with three successive doses of VB at 3, 4.5, and 6 mg/kg.
Results:
The results demonstrated a significant frequency of DNA fragmentation in spleen cells and in the percentage of CAs in bone marrow. Numerical and structural aberrations were recorded with a pronounced number of polyploidy metaphases which reached (11.60%) after treatment with 6 mg/kg for three successive days vs zero for control. VB also induced a significant percentage of CAs in spermatocytes in the form of univalent. Sperm defects in the form of coiled tail, absence of acrosome and shapeless head and a significant DNA damage in the testes were recorded. The frequency of sperm abnormalities reached 11.06 ± 0.14 after treatment with highest tested dose (6 mg/kg) vs 3.04 ± 0.19 for control.
Conclusion:
VB is genotoxic in somatic and germ cells. Sperm defects induced by VB are of serious concern to future generations and may affect the fertility of cancer survivors.
Insights
Vinblastine (VB) causes DNA damage in mice's somatic and germ cells. This chemotherapy drug induces sperm defects, raising concerns for cancer survivors' fertility and future generations.
Area of Science:
- Toxicology
- Genetics
- Reproductive Biology
Background:
- Chemotherapy can lead to secondary tumors due to genotoxicity.
- Sperm defects are a known complication of chemotherapy treatment.
- This study investigates the genotoxicity of vinblastine (VB) in somatic and germ cells.
Purpose of the Study:
- To assess the genotoxic effects of vinblastine (VB) on somatic and germ cells in a mouse model.
- To evaluate DNA damage and chromosomal aberrations induced by VB.
- To determine the impact of VB on sperm morphology and quality.
Main Methods:
- Mice were administered single or successive doses of vinblastine (VB) at varying concentrations (3-10 mg/kg).
- Chromosomal aberrations (CAs), DNA fragmentation (comet assay), and sperm abnormalities were analyzed.
- Somatic cells (bone marrow, spleen) and germ cells (spermatocytes, testes) were examined.
Main Results:
- Vinblastine significantly increased DNA fragmentation in spleen cells and CAs in bone marrow.
- Polyploidy metaphases reached 11.60% at the highest dose, indicating significant chromosomal damage.
- VB induced significant CAs in spermatocytes, sperm defects (coiled tail, absent acrosome), and DNA damage in testes.
Conclusions:
- Vinblastine exhibits genotoxicity in both somatic and germ cells.
- VB-induced sperm defects pose a serious risk to the fertility of cancer survivors.
- The findings highlight potential long-term reproductive health concerns for individuals treated with vinblastine.
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