PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 8980395-0 1996 Acceleration of MRP-associated efflux of rhodamine 123 by genistein and related compounds. Genistein 58-67 ATP binding cassette subfamily C member 1 Homo sapiens 16-19 27033456-7 2016 ABCC1 induction by GNT in MDA-MB-231 cells modified neither drug efflux nor chemoresistance due to simultaneous acute inhibition of the transporter activity by GNT. Genistein 19-22 ATP binding cassette subfamily C member 1 Homo sapiens 0-5 18634814-3 2008 We showed that 24 h after a single dose treatment with genistein, resveratrol or bisphenol A, the expression of ATP-binding cassette transporters (the multidrug resistance or MDR, and the multidrug resistance associated proteins or MRP) uridine diphosphate-glucuronosyltransferases (UGT) and/or sulfotransferases (ST) involved in 17beta-estradiol elimination process were significantly modulated and that 17beta-estradiol cellular flow was modified. Genistein 55-64 ATP binding cassette subfamily C member 1 Homo sapiens 232-235 12532374-9 2003 These results therefore indicate that the flavonoids morin, chalcone, silymarin, phloretin, genistein, quercetin, biochanin A, and kaempferol can inhibit MRP1-mediated drug transport, effects that may involve binding interactions with MRP1, as well as modulation of GSH concentrations. Genistein 92-101 ATP binding cassette subfamily C member 1 Homo sapiens 154-158 12532374-9 2003 These results therefore indicate that the flavonoids morin, chalcone, silymarin, phloretin, genistein, quercetin, biochanin A, and kaempferol can inhibit MRP1-mediated drug transport, effects that may involve binding interactions with MRP1, as well as modulation of GSH concentrations. Genistein 92-101 ATP binding cassette subfamily C member 1 Homo sapiens 235-239 12373300-7 2002 MRP1 mediated efflux of CFDA was analysed in the presence of DHT, the known substrates genistein, probenecid, and the specific inhibitor MK-571. Genistein 87-96 ATP binding cassette subfamily C member 1 Homo sapiens 0-4 25741749-8 2015 Also, cellular glucuronidation of genistein (38.3% for MRP1, 32.3% for MRP3, and 31.1% for MRP4; p < 0.01) and apigenin (40.6% for MRP1, 32.4% for MRP3, and 34.6% for MRP4; p < 0.001) was markedly suppressed. Genistein 34-43 ATP binding cassette subfamily C member 1 Homo sapiens 55-59 25741749-8 2015 Also, cellular glucuronidation of genistein (38.3% for MRP1, 32.3% for MRP3, and 31.1% for MRP4; p < 0.01) and apigenin (40.6% for MRP1, 32.4% for MRP3, and 34.6% for MRP4; p < 0.001) was markedly suppressed. Genistein 34-43 ATP binding cassette subfamily C member 1 Homo sapiens 134-138 15004974-3 2003 The MDR phenotype of the tumors was determined by a change in doxorubicin intracellular accumulation under the action of the ABC-transporter(s)" inhibitors: verapamil and genistein (specific inhibitors of Pgp and MRP respectively) and sodium azide (an inhibitor of all energy-dependent ABC-transporters). Genistein 171-180 ATP binding cassette subfamily C member 1 Homo sapiens 213-216 11448450-3 2001 We now demonstrate that other inhibitors of MRP1-mediated drug transport (e.g. MK571, indomethacin, genistein, and nifedipine) deplete cellular glutathione in these leukaemia cells (>30% decrease; P < 0.01) while having no effect on the parental CCRF-CEM cells. Genistein 100-109 ATP binding cassette subfamily C member 1 Homo sapiens 44-48 8548874-9 1996 However, genistein, which is a specific inhibitor of multidrug resistance-associated protein (MRP), increased the THP remaining in the resistant cells, and the value was approximately equal to that of the control group in the sensitive cells. Genistein 9-18 ATP binding cassette subfamily C member 1 Homo sapiens 94-97 8909298-11 1996 Genistein, an MRP-specific modulating agent, and arsenate, a compound for which MRP has previously been reported to confer resistance, were also competitive inhibitors, with Ki values of 17 and 29 microM, respectively. Genistein 0-9 ATP binding cassette subfamily C member 1 Homo sapiens 14-17 8909298-11 1996 Genistein, an MRP-specific modulating agent, and arsenate, a compound for which MRP has previously been reported to confer resistance, were also competitive inhibitors, with Ki values of 17 and 29 microM, respectively. Genistein 0-9 ATP binding cassette subfamily C member 1 Homo sapiens 80-83 7945406-0 1994 Competitive inhibition by genistein and ATP dependence of daunorubicin transport in intact MRP overexpressing human small cell lung cancer cells. Genistein 26-35 ATP binding cassette subfamily C member 1 Homo sapiens 91-94