Title : Induction of multidrug resistance gene expression in rat liver cells in response to acute treatment by the DNA-damaging agent methyl methanesulfonate.

Pub. Date : 1998 Apr 7

PMID : 9535788






7 Functional Relationships(s)
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1 Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS). Methyl Methanesulfonate ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
2 Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS). Methyl Methanesulfonate ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
3 Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS). Methyl Methanesulfonate ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
4 Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS). Methyl Methanesulfonate ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
5 In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells. Methyl Methanesulfonate ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
6 In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells. Methyl Methanesulfonate ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
7 In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells. Methyl Methanesulfonate ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus