ABCC10, ABCC11, and ABCC12
- PMID: 16868766
- DOI: 10.1007/s00424-006-0114-1
ABCC10, ABCC11, and ABCC12
Abstract
Multidrug resistance protein (MRP)7, MRP8, and MRP9 (gene symbols ABCC10, ABCC11, and ABCC12) are recently identified members of the MRP family that are at relatively early stages of investigation. Of these proteins, a physiological function has only been established for MRP8, for which a single nucleotide polymorphism determines wet vs dry earwax type. MRP7 and MRP8 are lipophilic anion pumps that are able to confer resistance to chemotherapeutic agents. MRP7 is competent in the transport of the glucuronide E(2)17betaG, and its resistance profile, which includes several natural product anticancer agents, is distinguished by the taxane docetaxel. MRP8 is able to transport a diverse range of lipophilic anions, including cyclic nucleotides, E(2)17betaG, steroid sulfates such as dehydroepiandrosterone (DHEAS) and E(1)S, glutathione conjugates such as leukotriene C4 and dinitrophenyl-S-glutathione, and monoanionic bile acids. However, the constituent of earwax that is susceptible to transport by MRP8 has not been identified. MRP8 has complex interactions with its substrates, as indicated by the nonreciprocal ability of DHEAS to stimulate E(2)17betaG transport. Similar to the case for other MRPs that possess only two membrane spanning domains (MRP4 and MRP5), MRP8 is a cyclic nucleotide efflux pump that is able to confer resistance to nucleoside-based agents, such as PMEA and 5FU. The functional characteristics of MRP9 are currently unknown.
Similar articles
-
Transport of bile acids, sulfated steroids, estradiol 17-beta-D-glucuronide, and leukotriene C4 by human multidrug resistance protein 8 (ABCC11).Mol Pharmacol. 2005 Feb;67(2):545-57. doi: 10.1124/mol.104.007138. Epub 2004 Nov 10. Mol Pharmacol. 2005. PMID: 15537867
-
Substrates and inhibitors of human multidrug resistance associated proteins and the implications in drug development.Curr Med Chem. 2008;15(20):1981-2039. doi: 10.2174/092986708785132870. Curr Med Chem. 2008. PMID: 18691054 Review.
-
Steroid and bile acid conjugates are substrates of human multidrug-resistance protein (MRP) 4 (ATP-binding cassette C4).Biochem J. 2003 Apr 15;371(Pt 2):361-7. doi: 10.1042/BJ20021886. Biochem J. 2003. PMID: 12523936 Free PMC article.
-
MRP8, ATP-binding cassette C11 (ABCC11), is a cyclic nucleotide efflux pump and a resistance factor for fluoropyrimidines 2',3'-dideoxycytidine and 9'-(2'-phosphonylmethoxyethyl)adenine.J Biol Chem. 2003 Aug 8;278(32):29509-14. doi: 10.1074/jbc.M304059200. Epub 2003 May 22. J Biol Chem. 2003. PMID: 12764137
-
Multidrug resistance proteins (MRPs, ABCCs): importance for pathophysiology and drug therapy.Handb Exp Pharmacol. 2011;(201):299-323. doi: 10.1007/978-3-642-14541-4_8. Handb Exp Pharmacol. 2011. PMID: 21103974 Review.
Cited by
-
Regulation of hepatic ABCC transporters by xenobiotics and in disease states.Drug Metab Rev. 2010 Aug;42(3):482-538. doi: 10.3109/03602531003654915. Drug Metab Rev. 2010. PMID: 20233023 Free PMC article. Review.
-
Identification of candidate ATP-binding cassette transporter gene family members in Diaphorina citri (Hemiptera: Psyllidae) via adult tissues transcriptome analysis.Sci Rep. 2019 Nov 1;9(1):15842. doi: 10.1038/s41598-019-52402-3. Sci Rep. 2019. PMID: 31676883 Free PMC article.
-
Recent advances regarding the role of ABC subfamily C member 10 (ABCC10) in the efflux of antitumor drugs.Chin J Cancer. 2014 May;33(5):223-30. doi: 10.5732/cjc.013.10122. Epub 2013 Oct 9. Chin J Cancer. 2014. PMID: 24103790 Free PMC article. Review.
-
Recent perspectives in ocular drug delivery.Pharm Res. 2009 May;26(5):1197-216. doi: 10.1007/s11095-008-9694-0. Epub 2008 Aug 29. Pharm Res. 2009. PMID: 18758924 Free PMC article. Review.
-
The small molecule tyrosine kinase inhibitor NVP-BHG712 antagonizes ABCC10-mediated paclitaxel resistance: a preclinical and pharmacokinetic study.Oncotarget. 2015 Jan 1;6(1):510-21. doi: 10.18632/oncotarget.2638. Oncotarget. 2015. PMID: 25402202 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous