Please use this identifier to cite or link to this item:
https://hdl.handle.net/1959.11/61687
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lu, Jamie F | en |
dc.contributor.author | Pokharel, Deep | en |
dc.contributor.author | Bebawy, Mary | en |
dc.date.accessioned | 2024-07-16T23:44:23Z | - |
dc.date.available | 2024-07-16T23:44:23Z | - |
dc.date.issued | 2015-10 | - |
dc.identifier.citation | Drug Metabolism Reviews, 47(4), p. 406-419 | en |
dc.identifier.issn | 1097-9883 | en |
dc.identifier.issn | 0360-2532 | en |
dc.identifier.uri | https://hdl.handle.net/1959.11/61687 | - |
dc.description.abstract | <p>The phenomenon of multidrug resistance (MDR) in cancer is associated with the overexpression of the ATP-binding cassette (ABC) transporter proteins, including multidrug resistance-associated protein 1 (MRP1) and P-glycoprotein. MRP1 plays an active role in protecting cells by its ability to efflux a vast array of drugs to sub-lethal levels. There has been much effort in elucidating the mechanisms of action, structure and substrates and substrate binding sites of MRP1 in the last decade. In this review, we detail our current understanding of MRP1, its clinical relevance and highlight the current environment in the search for MRP1 inhibitors. We also look at the capacity for the rapid intercellular transfer of MRP1 phenotype from spontaneously shed membrane vesicles known as microparticles and discuss the clinical and therapeutic significance of this in the context of cancer MDR.</p> | en |
dc.language | en | en |
dc.publisher | Taylor & Francis Inc | en |
dc.relation.ispartof | Drug Metabolism Reviews | en |
dc.title | MRP1 and its role in anticancer drug resistance | en |
dc.type | Journal Article | en |
dc.identifier.doi | 10.3109/03602532.2015.1105253 | en |
dc.identifier.pmid | 26541366 | en |
local.contributor.firstname | Jamie F | en |
local.contributor.firstname | Deep | en |
local.contributor.firstname | Mary | en |
local.profile.school | School of Psychology | en |
local.profile.email | mbebawy@une.edu.au | en |
local.output.category | C1 | en |
local.record.place | au | en |
local.record.institution | University of New England | en |
local.publisher.place | United States of America | en |
local.format.startpage | 406 | en |
local.format.endpage | 419 | en |
local.peerreviewed | Yes | en |
local.identifier.volume | 47 | en |
local.identifier.issue | 4 | en |
local.contributor.lastname | Lu | en |
local.contributor.lastname | Pokharel | en |
local.contributor.lastname | Bebawy | en |
dc.identifier.staff | une-id:mbebawy | en |
local.profile.orcid | 0000-0003-2606-921X | en |
local.profile.role | author | en |
local.profile.role | author | en |
local.profile.role | author | en |
local.identifier.unepublicationid | une:1959.11/61687 | en |
dc.identifier.academiclevel | Academic | en |
dc.identifier.academiclevel | Academic | en |
dc.identifier.academiclevel | Academic | en |
local.title.maintitle | MRP1 and its role in anticancer drug resistance | en |
local.output.categorydescription | C1 Refereed Article in a Scholarly Journal | en |
local.search.author | Lu, Jamie F | en |
local.search.author | Pokharel, Deep | en |
local.search.author | Bebawy, Mary | en |
local.uneassociation | No | en |
local.atsiresearch | No | en |
local.sensitive.cultural | No | en |
local.year.published | 2015 | en |
local.fileurl.closedpublished | https://rune.une.edu.au/web/retrieve/c507533c-2bce-4f0f-8ccd-b292531ee10a | en |
local.subject.for2020 | 3208 Medical physiology | en |
local.profile.affiliationtype | External Affiliation | en |
local.profile.affiliationtype | External Affiliation | en |
local.profile.affiliationtype | External Affiliation | en |
local.date.moved | 2024-07-30 | en |
Appears in Collections: | Journal Article School of Psychology |
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