Influence of cell cycle on responses of MCF-7 cells to benzo[a]pyrene

<p>Abstract</p> <p>Background</p> <p>Benzo[a]pyrene (BaP) is a widespread environmental genotoxic carcinogen that damages DNA by forming adducts. This damage along with activation of the aryl hydrocarbon receptor (AHR) induces complex transcriptional responses in cells. To investigate whether human cells are more susceptible to BaP in a particular phase of the cell cycle, synchronised breast carcinoma MCF-7 cells were exposed to BaP. Cell cycle progression was analysed by flow cytometry, DNA adduct formation was assessed by ³²P-postlabeling analysis, microarrays of 44K human genome-wide oligos and RT-PCR were used to detect gene expression (mRNA) changes and Western blotting was performed to determine the expression of some proteins, including cytochrome P450 (CYP) 1A1 and CYP1B1, which are involved in BaP metabolism.</p> <p>Results</p> <p>Following BaP exposure, cells evaded <it>G1 </it>arrest and accumulated in <it>S</it>-phase. Higher levels of DNA damage occurred in <it>S</it>- and <it>G2/M</it>- compared with <it>G0/G1-</it>enriched cultures. Genes that were found to have altered expression included those involved in xenobiotic metabolism, apoptosis, cell cycle regulation and DNA repair. Gene ontology and pathway analysis showed the involvement of various signalling pathways in response to BaP exposure, such as the Catenin/Wnt pathway in <it>G1</it>, the ERK pathway in <it>G1 </it>and <it>S</it>, the Nrf2 pathway in <it>S </it>and <it>G2/M </it>and the Akt pathway in <it>G2/M</it>. An important finding was that higher levels of DNA damage in <it>S- </it>and <it>G2/M</it>-enriched cultures correlated with higher levels of <it>CYP1A1 </it>and <it>CYP1B1 </it>mRNA and proteins. Moreover, exposure of synchronised MCF-7 cells to BaP-7,8-diol-9,10-epoxide (BPDE), the ultimate carcinogenic metabolite of BaP, did not result in significant changes in DNA adduct levels at different phases of the cell cycle.</p> <p>Conclusions</p> <p>This study characterised the complex gene response to BaP in MCF-7 cells and revealed a strong correlation between the varying efficiency of BaP metabolism and DNA damage in different phases of the cell cycle. Our results suggest that growth kinetics within a target-cell population may be important determinants of susceptibility and response to a genotoxic agent.</p

Influence of cell-cycle kinetics on responses of human cells to a genotoxic carcinogen, benzo[a]pyrene

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