Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2116920 | Cancer Letters | 2006 | 11 Pages |
Abstract
MRPs are membrane proteins transporting organic anions at the expense of ATP hydrolysis. MRP2 is known to be a major transporter of organic anions from the liver into bile. We discuss recent results showing allosteric control of human but not rat MRP2. MRP3 has been considered a major player in bile salt metabolism, but our recent results with Mrp3 KO mice do not support this. Instead, we have found a role for MRP3 in the cellular export of drug–glucuronide conjugates. We discuss problems in extrapolating results obtained for murine MRPs.
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Authors
P. Borst, N. Zelcer, K. van de Wetering,