A common carcinogen benzo[a]pyrene causes p53 overexpression in mouse cervix via DNA damage

. [Display omitted] • The results showed that benzo[a]pyrene induced a significant and dose-dependent increase in the number of DNA damaged cells and the tail length as well as tail moment in cervical tissue. • The expression level of p53 protein and mRNA is significantly increased in cervical tissue of benzo[a]pyrene treated mice. • The increase in the expression of the p53 gene may be due to the DNA damage induced by benzo[a]pyrene in cervical tissue. Benzo[a]pyrene (BaP) is cytotoxic and/or genotoxic to lung, stomach and skin tissue in the body. However, the effect of BaP on cervical tissue remains unclear. The present study detected DNA damage and the expression of the p53 gene in BaP-induced cervical tissue in female mice. Animals were intraperitoneally injected and orally gavaged with BaP at the doses of 2.5, 5, and 10mg/kg twice a week for 14 weeks. The single-cell gel electrophoresis (SCGE) assay was used to detect the DNA damage. Immunohistochemistry (IHC) and in situ hybridization (ISH) were used to detect the expression of p53 protein and p53 mRNA, respectively. The results showed that BaP induced a significant and dose-dependent increase of the number of cells with DNA damaged and the tail length as well as Comet tail moment in cervical tissue. The expression level of p53 protein and mRNA was increased. The results demonstrate that BaP may show toxic effect on the cervix by increasing DNA damage and the expression of the p53 gene.