Evidence map›Paper›PMID 27709005›Full record

ReviewActa pharmaceutica Sinica. B2016

Renal drug transporters and their significance in drug-drug interactions.

Jia Yin, Joanne Wang

Abstract readReview
In one paragraph

Review in Acta pharmaceutica Sinica. B, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

87 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Advances in the Targeted Drug Delivery System for Renal Fibrosis.International journal of nanomedicine · 2026
    Review
  7. Article
  8. Review
  9. Review
  10. Novel emerging cell and organoid systems for the study of drug metabolism and toxicity in humans.Drug metabolism and disposition: the biological fate of chemicals · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

27 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Jia YinDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195-7610, USA.
Joanne WangDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195-7610, USA.

Funding

NRSA Training CoreTL1TR002318 · NCATS · UNIVERSITY OF WASHINGTON · PI Megan Moore · 2017 to 2026
$8.4M
The plasma membrane monoamine transporter (PMAT): expression and role in mIBG disposition in neuroblastomaR01GM066233 · NIGMS · UNIVERSITY OF WASHINGTON · PI WANG, JOANNE · 2002 to 2020
$5.1M
Institute of Translational Health SciencesTL1TR000422 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$2.1M
NCATS NIH HHS TL1 TR000422NCATS NIH HHS TL1 TR002318NIGMS NIH HHS R01 GM066233
6 · The paper itself

Abstract

The kidney is a vital organ for the elimination of therapeutic drugs and their metabolites. Renal drug transporters, which are primarily located in the renal proximal tubules, play an important role in tubular secretion and reabsorption of drug molecules in the kidney. Tubular secretion is characterized by high clearance capacities, broad substrate specificities, and distinct charge selectivity for organic cations and anions. In the past two decades, substantial progress has been made in understanding the roles of transporters in drug disposition, efficacy, toxicity and drug-drug interactions (DDIs). In the kidney, several transporters are involved in renal handling of organic cation (OC) and organic anion (OA) drugs. These transporters are increasingly recognized as the target for clinically significant DDIs. This review focuses on the functional characteristics of major human renal drug transporters and their involvement in clinically significant DDIs.

Indexed as

ABC, ATP-binding cassetteATP, adenosine triphosphateAUC, area under the plasma concentration curveBBB, blood–brain barrierCHO, Chinese hamster ovaryCL, plasma clearanceCLR, renal clearanceCmax, maximum plasma concentrationDDIs, drug–drug interactionsDrug–drug interactionsFDA, U.S. Food and Drug Administrationfe, fraction of the absorbed dose excreted unchanged in urineGSH, glutathioneHEK, human embryonic kidneyIC50, half maximal inhibitory concentrationITC, International Transporter ConsortiumKi, inhibitory constantMATE, multidrug and toxin extrusion proteinMPP+, 1-methyl-4-phenylpyridimiumMRP, multidrug resistance-associated proteinMSD, membrane-spanning domainMW, molecular weightNBD, nucleotide-binding domainNephrotoxicityNME, new molecular entityNSAID, non-steroidal anti-inflammatory drugsOA, organic anionOAT or Oat, organic anion transportersOATP or Oatp, organic anion-transporting peptideOC, organic cationOCTN, Organic zwitterions/cation transportersOCT or Oct, organic cation transporterOrganic anionsOrganic cationsPAH, p-aminohippurateP-gp, P-glycoproteinRenal drug transportersSLC, solute carrierSNP, single-nucleotide polymorphismTEA, tetraethylammoniumTMD, transmembrane domainURAT, urate transporter

Identifiers

PMID27709005
PMCPMC5045553

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.