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• W2918409259 abstract "The ATP-binding cassette transporter G2 (ABCG2; also known as breast cancer resistance protein, BCRP) has been suggested to be involved in clinical multidrug resistance (MDR) in cancer like other ABC transporters such as ABCB1 (P-glycoprotein). As an efflux pump exhibiting a broad substrate specificity localized on cellular plasma membrane, ABCG2 excretes a variety of endogenous and exogenous substrates including chemotherapeutic agents, such as mitoxantrone and several tyrosine kinase inhibitors. Moreover, in the normal tissues, ABCG2 is expressed on the apical membranes and plays a pivotal role in tissue protection against various xenobiotics. For this reason, ABCG2 is recognized to be an important determinant of the pharmacokinetic characteristics of its substrate drugs. Although the clinical relevance of reversing the ABCG2-mediated MDR has been inconclusive, an appropriate modulation of ABCG2 function during chemotherapy should logically enhance the efficacy of anti-cancer agents by overcoming the MDR phenotype and/or improving their pharmacokinetics. To confirm this possibility, considerable efforts have been devoted to developing ABCG2 inhibitors, although there is no clinically available substance for this purpose. As a clue for addressing this issue, this mini-review provides integrated information covering the technical backgrounds necessary to evaluate the ABCG2 inhibitory effects on the target compounds and a current update on the ABCG2 inhibitors. This essentially includes our recent findings, as we serendipitously identified febuxostat, a well-used agent for hyperuricemia as a strong ABCG2 inhibitor, that possesses some promising potentials. We hope that an overview described here will add value to further studies involving in the multidrug transporters." @default.
• W2918409259 created "2019-03-11" @default.
• W2918409259 creator A5010418421 @default.
• W2918409259 creator A5021909900 @default.
• W2918409259 creator A5068200348 @default.
• W2918409259 date "2019-03-05" @default.
• W2918409259 modified "2023-10-18" @default.
• W2918409259 title "Inhibitors of Human ABCG2: From Technical Background to Recent Updates With Clinical Implications" @default.
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• W2918409259 doi "https://doi.org/10.3389/fphar.2019.00208" @default.
• W2918409259 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6411714" @default.
• W2918409259 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30890942" @default.
• W2918409259 hasPublicationYear "2019" @default.
• W2918409259 type Work @default.
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