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Multidrug resistance associated proteins in multidrug resistance
Multidrug resistance proteins (MRPs) are members of the C family of a group of proteins named ATP-binding cassette (ABC) transporters. These ABC transporters together form the largest branch of proteins within the human body. The MRP family comprises of 13 members, of which MRP1 to MRP9 are the majo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Sun Yat-sen University Cancer Center
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777468/ https://www.ncbi.nlm.nih.gov/pubmed/22098952 http://dx.doi.org/10.5732/cjc.011.10329 |
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author | Sodani, Kamlesh Patel, Atish Kathawala, Rishil J. Chen, Zhe-Sheng |
author_facet | Sodani, Kamlesh Patel, Atish Kathawala, Rishil J. Chen, Zhe-Sheng |
author_sort | Sodani, Kamlesh |
collection | PubMed |
description | Multidrug resistance proteins (MRPs) are members of the C family of a group of proteins named ATP-binding cassette (ABC) transporters. These ABC transporters together form the largest branch of proteins within the human body. The MRP family comprises of 13 members, of which MRP1 to MRP9 are the major transporters indicated to cause multidrug resistance in tumor cells by extruding anticancer drugs out of the cell. They are mainly lipophilic anionic transporters and are reported to transport free or conjugates of glutathione (GSH), glucuronate, or sulphate. In addition, MRP1 to MRP3 can transport neutral organic drugs in free form in the presence of free GSH. Collectively, MRPs can transport drugs that differ structurally and mechanistically, including natural anticancer drugs, nucleoside analogs, antimetabolites, and tyrosine kinase inhibitors. Many of these MRPs transport physiologically important anions such as leukotriene C4, bilirubin glucuronide, and cyclic nucleotides. This review focuses mainly on the physiological functions, cellular resistance characteristics, and probable in vivo role of MRP1 to MRP9. |
format | Online Article Text |
id | pubmed-3777468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Sun Yat-sen University Cancer Center |
record_format | MEDLINE/PubMed |
spelling | pubmed-37774682013-12-11 Multidrug resistance associated proteins in multidrug resistance Sodani, Kamlesh Patel, Atish Kathawala, Rishil J. Chen, Zhe-Sheng Chin J Cancer Review Multidrug resistance proteins (MRPs) are members of the C family of a group of proteins named ATP-binding cassette (ABC) transporters. These ABC transporters together form the largest branch of proteins within the human body. The MRP family comprises of 13 members, of which MRP1 to MRP9 are the major transporters indicated to cause multidrug resistance in tumor cells by extruding anticancer drugs out of the cell. They are mainly lipophilic anionic transporters and are reported to transport free or conjugates of glutathione (GSH), glucuronate, or sulphate. In addition, MRP1 to MRP3 can transport neutral organic drugs in free form in the presence of free GSH. Collectively, MRPs can transport drugs that differ structurally and mechanistically, including natural anticancer drugs, nucleoside analogs, antimetabolites, and tyrosine kinase inhibitors. Many of these MRPs transport physiologically important anions such as leukotriene C4, bilirubin glucuronide, and cyclic nucleotides. This review focuses mainly on the physiological functions, cellular resistance characteristics, and probable in vivo role of MRP1 to MRP9. Sun Yat-sen University Cancer Center 2012-02 /pmc/articles/PMC3777468/ /pubmed/22098952 http://dx.doi.org/10.5732/cjc.011.10329 Text en Chinese Journal of Cancer http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission. |
spellingShingle | Review Sodani, Kamlesh Patel, Atish Kathawala, Rishil J. Chen, Zhe-Sheng Multidrug resistance associated proteins in multidrug resistance |
title | Multidrug resistance associated proteins in multidrug resistance |
title_full | Multidrug resistance associated proteins in multidrug resistance |
title_fullStr | Multidrug resistance associated proteins in multidrug resistance |
title_full_unstemmed | Multidrug resistance associated proteins in multidrug resistance |
title_short | Multidrug resistance associated proteins in multidrug resistance |
title_sort | multidrug resistance associated proteins in multidrug resistance |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777468/ https://www.ncbi.nlm.nih.gov/pubmed/22098952 http://dx.doi.org/10.5732/cjc.011.10329 |
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