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- W2022810014 abstract "Rat 6 cells are not transformed by treatment with the wellknown carcinogens benzo(a)pyrene (BP) or N-methyl-N-nitro-N' nitrosoguanidine (MNNG). Upon retroviral transduction of the mouse c-myc gene, Rat 6 cells showed mildly altered morphology and formed microcolonies in soft agar; furthermore, they could be transformed by BP and MNNG to form large colonies in agar (Hsiao et al. (1992) Mol. Carcinogenesis, 5, 140-154). In the current report, We tested the sensitivity of the c-myc-overexpressing cells (Rat 6/c-myc) to two additional chemicals: 5-azacytidine and MnSO4. These chemicals differ from the direct-acting mutagens tested previously. 5-Azacytidine, a potent DNA methylation inhibitor, induced growth of large colonies in soft agar cultures of Rat 6 or Rat 6/c-myc cells. On the other hand, MnSO4 only induced transformation in Rat 6/c-myc cells, but not the parental Rat 6 cells. Transformants induced by 5-azacytidine lost c-myc-induced apoptotic cell death, whereas degree MnSO4 induced transformants showed a higher degree of apoptosis than the parental Rat 6/c-myc cells.These results suggest that MnSO4 co-operates with over-expressed c-myc in including transformation, while 5-azacytidine transformetion and may involve alterations in the regulation of apoptosis." @default.
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- W2022810014 date "1996-01-01" @default.
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- W2022810014 title "Comparison of transformation by manganese sulfate and 5-azacytidine in Rat 6 cells overexpressing the <i>c-myc</i> oncogene" @default.
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- W2022810014 doi "https://doi.org/10.1093/carcin/17.12.2771" @default.
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