Multidrug resistance proteins (MRPs): Structure, function and the overcoming of cancer multidrug resistance.
ABC transporter
Cancer chemotherapy
MRP
Multidrug resistance protein
Journal
Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy
ISSN: 1532-2084
Titre abrégé: Drug Resist Updat
Pays: Scotland
ID NLM: 9815369
Informations de publication
Date de publication:
01 2021
01 2021
Historique:
received:
16
10
2020
revised:
21
12
2020
accepted:
25
12
2020
pubmed:
30
1
2021
medline:
25
12
2021
entrez:
29
1
2021
Statut:
ppublish
Résumé
ATP-binding cassette (ABC) transporters mediate the ATP-driven translocation of structurally and mechanistically distinct substrates against steep concentration gradients. Among the seven human ABC subfamilies namely ABCA-ABCG, ABCC is the largest subfamily with 13 members. In this respect, 9 of the ABCC members are termed "multidrug resistance proteins" (MRPs1-9) due to their ability to mediate cancer multidrug resistance (MDR) by extruding various chemotherapeutic agents or their metabolites from tumor cells. Furthermore, MRPs are also responsible for the ATP-driven efflux of physiologically important organic anions such as leukotriene C
Identifiants
pubmed: 33513557
pii: S1368-7646(21)00001-7
doi: 10.1016/j.drup.2021.100743
pii:
doi:
Substances chimiques
ATP Binding Cassette Transporter, Subfamily B
0
Antineoplastic Agents
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
100743Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.