New and Emerging Research on Solute Carrier and ATP Binding Cassette Transporters in Drug Discovery and Development: Outlook from the International Transporter Consortium

被引:29
作者
Giacomini, Kathleen M. [1 ]
Yee, Sook W. [1 ]
Koleske, Megan L. [1 ]
Zou, Ling [2 ]
Matsson, Par [3 ]
Chen, Eugene C. [4 ]
Kroetz, Deanna L. [1 ]
Miller, Miles A. [5 ]
Gozalpour, Elnaz [6 ]
Chu, Xiaoyan [7 ]
机构
[1] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[2] Amgen Inc, Pharmacokinet & Drug Metab, San Francisco, CA USA
[3] Univ Gothenburg, Sahlgrenska Acad, Dept Pharmacol, Gothenburg, Sweden
[4] Genentech Inc, Dept Drug Metab & Pharmacokinet, San Francisco, CA 94080 USA
[5] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[6] AstraZeneca R&D, Drug Safety & Metab, IMED Biotech Unit, Safety & ADME Translat Sci Dept, Cambridge, England
[7] Merck & Co Inc, Dept ADME & Discovery Toxicol, Kenilworth, NJ 07033 USA
基金
美国国家卫生研究院;
关键词
IN-VITRO; GLYCEMIC RESPONSE; SLC TRANSPORTERS; PROXIMAL TUBULE; P-GLYCOPROTEIN; LIVER; METABOLISM; INHIBITION; KIDNEY; RESISTANCE;
D O I
10.1002/cpt.2627
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Enabled by a plethora of new technologies, research in membrane transporters has exploded in the past decade. The goal of this state-of-the-art article is to describe recent advances in research on membrane transporters that are particularly relevant to drug discovery and development. This review covers advances in basic, translational, and clinical research that has led to an increased understanding of membrane transporters at all levels. At the basic level, we describe the available crystal structures of membrane transporters in both the solute carrier (SLC) and ATP binding cassette superfamilies, which has been enabled by the development of cryogenic electron microscopy methods. Next, we describe new research on lysosomal and mitochondrial transporters as well as recently deorphaned transporters in the SLC superfamily. The translational section includes a summary of proteomic research, which has led to a quantitative understanding of transporter levels in various cell types and tissues and new methods to modulate transporter function, such as allosteric modulators and targeted protein degraders of transporters. The section ends with a review of the effect of the gut microbiome on modulation of transporter function followed by a presentation of 3D cell cultures, which may enable in vivo predictions of transporter function. In the clinical section, we describe new genomic and pharmacogenomic research, highlighting important polymorphisms in transporters that are clinically relevant to many drugs. Finally, we describe new clinical tools, which are becoming increasingly available to enable precision medicine, with the application of tissue-derived small extracellular vesicles and real-world biomarkers.
引用
收藏
页码:540 / 561
页数:22
相关论文
共 149 条
[1]   Liquid Biopsy Enables Quantification of the Abundance and Interindividual Variability of Hepatic Enzymes and Transporters [J].
Achour, Brahim ;
Al-Majdoub, Zubida M. ;
Grybos-Gajniak, Agnieszka ;
Lea, Kristi ;
Kilford, Peter ;
Zhang, Mian ;
Knight, David ;
Barber, Jill ;
Schageman, Jeoffrey ;
Rostami-Hodjegan, Amin .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2021, 109 (01) :222-232
[2]   Structural insight into substrate and inhibitor discrimination by human P-glycoprotein [J].
Alam, Amer ;
Kowal, Julia ;
Broude, Eugenia ;
Roninson, Igor ;
Locher, Kaspar P. .
SCIENCE, 2019, 363 (6428) :753-+
[3]   Transporter-Mediated Alterations in Patients With NASH Increase Systemic and Hepatic Exposure to an OATP and MRP2 Substrate [J].
Ali, Izna ;
Slizgi, Jason R. ;
Kaullen, Josh D. ;
Ivanovic, Marija ;
Niemi, Mikko ;
Stewart, Paul W. ;
Barritt, Alfred S. ;
Brouwer, Kim L. R. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2018, 104 (04) :749-756
[4]   Eltrombopag increases plasma rosuvastatin exposure in healthy volunteers [J].
Allred, Alicia J. ;
Bowen, Carolyn J. ;
Park, Jung Wook ;
Peng, Bin ;
Williams, Daphne D. ;
Wire, Mary Beth ;
Lee, Edmund .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2011, 72 (02) :321-329
[5]  
[Anonymous], 2014, NATURE, V506, P97, DOI [DOI 10.1038/nature12828, 10.1038/nature12828]
[6]  
Bai XY, 2017, MOL MEMBR BIOL, V34, P1, DOI 10.1080/09687688.2018.1448123
[7]   Bioluminescent imaging of drug efflux at the blood-brain barrier mediated by the transporter ABCG2 [J].
Bakhsheshian, Joshua ;
Wei, Bih-Rong ;
Chang, Ki-Eun ;
Shukla, Suneet ;
Ambudkar, Suresh V. ;
Simpson, R. Mark ;
Gottesman, Michael M. ;
Hall, Matthew D. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (51) :20801-20806
[8]   Characterization of drug-induced human mitochondrial ADP/ATP carrier inhibition [J].
Baron, Stephany Jaiquel ;
King, Martin S. ;
Kunji, Edmund R. S. ;
Schirris, Tom J. J. .
THERANOSTICS, 2021, 11 (11) :5077-5091
[9]   Development of a human primary gut-on-a-chip to model inflammatory processes [J].
Beaurivage, Claudia ;
Kanapeckaite, Auste ;
Loomans, Cindy ;
Erdmann, Kai S. ;
Stallen, Jan ;
Janssen, Richard A. J. .
SCIENTIFIC REPORTS, 2020, 10 (01)
[10]  
Bendayan R., CLIN PHARMACOL THER