Evidence mapPaperPMID 41722177Full record

ReviewPharmacological reviews2026

Role of solute carrier transporters in the biodistribution and toxicity of chemotherapeutic drugs.

Mike Boeckman, Thomas Drabison, Arthur Germakovski, Allison Warmuth, Bagdad Ahmed, Anika T Chowdhury, Shuiying Hu, Jason A Sprowl, Alex Sparreboom, Kevin M Huang

Abstract readReview
In one paragraph

Review in Pharmacological reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
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

1 citing paper in PubMed.

  1. Review
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

10 authors.

Mike BoeckmanDivision of Pharmaceutics and Pharmacology, College of Pharmacy & Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Thomas DrabisonDivision of Pharmaceutics and Pharmacology, College of Pharmacy & Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Arthur GermakovskiDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Division of Molecular Biosciences, University at Buffalo, Buffalo, New York.
Allison WarmuthDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Division of Molecular Biosciences, University at Buffalo, Buffalo, New York.
Bagdad AhmedDivision of Pharmaceutics and Pharmacology, College of Pharmacy & Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Anika T ChowdhuryDivision of Pharmaceutics and Pharmacology, College of Pharmacy & Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Shuiying HuDivision of Pharmaceutics and Pharmacology, College of Pharmacy & Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Jason A SprowlDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Division of Molecular Biosciences, University at Buffalo, Buffalo, New York.
Alex SparreboomDivision of Pharmaceutics and Pharmacology, College of Pharmacy & Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio. Electronic address: sparreboom.1@osu.edu.
Kevin M HuangDivision of Pharmaceutics and Pharmacology, College of Pharmacy & Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.

Funding

The Chesapeake-Ohio Pharmacokinetics Core for The ETCTNU24CA247648 · NCI · JOHNS HOPKINS UNIVERSITY · 2023 to 2025
$1.0M
Therapeutic Strategies to Mitigate Toxicities of Anthracycline-Based TherapeuticsR01HL168045 · OHIO STATE UNIVERSITY · 2025 to 2025
$746k
Targeting neuronal transport to ameliorate vincristine neurotoxicityR01CA272254 · OHIO STATE UNIVERSITY · 2025 to 2025
$652k
Regulation of hepatic uptake transporters by tyrosine kinasesR01GM139936 · STATE UNIVERSITY OF NEW YORK AT BUFFALO · 2025 to 2025
$464k
NCI NIH HHS R01 CA272254NIDCD NIH HHS R21 DC021031NIGMS NIH HHS R01 GM139936NIH HHS R01HL168045NIH National Institutes of Health R21DC021031NIH National Institutes of Health U24CA247648
6 · The paper itself

Abstract

Our understanding of the solute carrier (SLC) family of transporters has greatly increased in recent years, especially in oncology, and a wealth of information is now available, indicating that certain SLC family members contribute to the cellular accumulation of small-molecule cancer drugs at sites of injury and to unwanted toxicity in normal tissues. The present review aimed to provide an overview of the toxic effects of commonly used chemotherapy drugs that are associated with SLC-mediated transport, how these associations have been derived, what ensuing intervention strategies have been explored, and how the investigation of these phenomena might change in the near future with the availability of increasingly sophisticated and innovative models and techniques. It is expected that this rapidly emerging field continues to contribute to filling our gaps in knowledge and will aid in the development of interventions aimed at preventing debilitating side effects of cancer drugs and improving the quality of life. SIGNIFICANCE STATEMENT: Toxicities associated with small-molecule chemotherapeutics can be debilitating or even life-threatening and pose a burden on the healthcare system. Improving our understanding of the initiating transporter-mediated mechanisms of these side effects is crucial to the development of preventative or treatment strategies.

Indexed as

Antineoplastic AgentsMembrane Transport ProteinsAnimalsBiological TransportHumansNeoplasmsTissue DistributionAntineoplastic AgentsMembrane Transport Proteins

Identifiers

PMID41722177
PMCPMC13084601

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.