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Updated: Jul 16, 2026

Clonogenic Assay: Adherent Cells
Published on: March 13, 2011
Evaluation of the clastogenicity and anticlastogenicity of vitamin B6 in human lymphocyte cultures
Paula Lumy Takeuchi1, Lusânia Maria Greggi Antunes, Catarina Satie Takahashi
1Departamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto (SP), Brazil. paulinha_lumyt@hotmail.com
Abstract:
Insufficient intakes of many micronutrients found in fruits and vegetables, such as folic acid, vitamins C and B6 may lead to DNA damage, cancer, and degenerative disease. The investigation of dietary antioxidants is a field of great interest for elucidating mechanisms of mutagenesis/carcinogenesis. The present study was undertaken to investigate the effects of vitamin B6 on the induction of chromosomal aberrations in cultured human lymphocytes and to examine the possible anticlastogenic effect of this vitamin on chromosomal damage induced by the antitumor drug doxorubicin. The results showed that when the cultures treated with vitamin B6 were compared with the untreated control in terms of total chromosomal damage and abnormal metaphases, pre- and simultaneous treatment with this vitamin showed no significant differences. In the post-treatment, average and above average concentrations of vitamin B6 alone showed a clastogenic effect. In the simultaneous protocol, this vitamin (15, 90 and 120 microg/mL) was effective in inhibiting chromosomal aberrations induced by doxorubicin (p<0.05), with a reduction of 33.1% with the highest concentration tested. However, in the post-treatment, the associations of vitamin B6 and doxorubicin exerted a more evident clastogenic effect than that observed in the cultures exposed only to the antitumor drug. In the present investigation, the inability of vitamin B6 to decrease chromosomal damage induced by doxorubicin in the pre- and post-treatments could be justified by the instability of this vitamin as a free radical scavenger. In conclusion, the results from this study confirmed that vitamin B6 is protective against chromosomal damage induced by doxorubicin in cultured human lymphocytes, but that the effects depend on concentration and form of treatment.
Insights
Vitamin B6 demonstrated protective effects against chromosomal damage induced by doxorubicin in human lymphocytes. However, its efficacy as an antioxidant depends on the treatment concentration and timing.
Area of Science:
- Biochemistry
- Genetics
- Nutritional Science
Background:
- Micronutrient deficiencies, including vitamin B6, are linked to DNA damage, cancer, and degenerative diseases.
- Dietary antioxidants are crucial for understanding mutagenesis and carcinogenesis.
- Vitamin B6's role in preventing chromosomal damage requires further investigation.
Purpose of the Study:
- To assess the effects of vitamin B6 on inducing chromosomal aberrations in human lymphocytes.
- To evaluate vitamin B6's potential to prevent chromosomal damage caused by the chemotherapy drug doxorubicin.
Main Methods:
- Cultured human lymphocytes were treated with varying concentrations of vitamin B6.
- Cells were exposed to doxorubicin, with vitamin B6 administered before, during, or after doxorubicin treatment.
- Chromosomal aberrations and abnormal metaphases were analyzed to assess damage and protection.
Main Results:
- Vitamin B6 alone at higher concentrations exhibited a clastogenic effect in post-treatment.
- Simultaneous treatment with vitamin B6 inhibited doxorubicin-induced chromosomal aberrations, with significant reduction at 120 microg/mL.
- Vitamin B6 did not prevent damage in pre- or post-treatment protocols, possibly due to its instability as a free radical scavenger.
Conclusions:
- Vitamin B6 offers protection against doxorubicin-induced chromosomal damage in human lymphocytes, but this effect is concentration-dependent.
- The timing of vitamin B6 administration is critical for its protective or detrimental effects.
- Further research is needed to understand the mechanisms underlying vitamin B6's variable effects on chromosomal integrity.
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