Evidence map›Paper›PMID 31832201›Full record

ArticlePharmacology research & perspectives2019

Role of equilibrative nucleoside transporter 1 (ENT1) in the disposition of cytarabine in mice.

Jason T Anderson, Shuiying Hu, Qiang Fu, Sharyn D Baker, Alex Sparreboom

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 22% of its field
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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Solute Carrier Transportome in Chemotherapy-Induced Adverse Drug Reactions.Reviews of physiology, biochemistry and pharmacology · 2022
    Article
  7. Article
  8. Article
  9. Article
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

5 authors at 1 institution in 1 country.

Jason T AndersonDivision of Pharmaceutics and Pharmacology College of Pharmacy and Comprehensive Cancer Center The Ohio State University Columbus OH USA.
Shuiying HuDivision of Pharmaceutics and Pharmacology College of Pharmacy and Comprehensive Cancer Center The Ohio State University Columbus OH USA.
Qiang FuDivision of Pharmaceutics and Pharmacology College of Pharmacy and Comprehensive Cancer Center The Ohio State University Columbus OH USA.
Sharyn D BakerDivision of Pharmaceutics and Pharmacology College of Pharmacy and Comprehensive Cancer Center The Ohio State University Columbus OH USA.ORCID 0000-0003-3062-3252
Alex SparreboomDivision of Pharmaceutics and Pharmacology College of Pharmacy and Comprehensive Cancer Center The Ohio State University Columbus OH USA.ORCID 0000-0003-2660-6644
The Ohio State University · US

Funding

Tyrosine kinase inhibitors for the treatment of childhood AMLR01CA138744 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI BAKER, SHARYN D · 2010 to 2019
$3.3M
Prevention of paclitaxel-induced peripheral neuropathy with nilotinibR01CA238946 · NCI · OHIO STATE UNIVERSITY · PI HU, SHUIYING, LUSTBERG, MARYAM B. · 2019 to 2023
$2.9M
(9) Therapeutic strategies to mitigate toxicities of platinum-based therapeuticsR01CA215802 · NCI · OHIO STATE UNIVERSITY · PI PABLA, NAVJOT, SPARREBOOM, ALEXANDER · 2017 to 2021
$2.5M
Solute Carriers and Oxaliplatin NeurotoxicityR01CA187176 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SPARREBOOM, ALEXANDER · 2015 to 2019
$1.8M
NCI NIH HHS R01 CA138744NCI NIH HHS R01 CA187176NCI NIH HHS R01 CA215802NCI NIH HHS R01 CA238946
6 · The paper itself

Abstract

Cytarabine (Ara-C) is a nucleoside analog used in the treatment of acute myeloid leukemia (AML). Despite the many years of clinical use, the identity of the transporter(s) involved in the disposition of Ara-C remains poorly studied. Previous work demonstrated that concurrent administration of Ara-C with nitrobenzylmercaptopurine ribonucleoside (NBMPR) causes an increase in Ara-C plasma levels, suggesting involvement of one or more nucleoside transporters. Here, we confirmed the presence of an NMBPR-mediated interaction with Ara-C resulting in a 2.5-fold increased exposure. The interaction was unrelated to altered blood cell distribution, and subsequent studies indicated that the disposition of Ara-C was unaffected in mice with a deficiency of postulated candidate transporters, including ENT1, OCTN1, OATP1B2, and MATE1. These studies indicate the involvement of an unknown NBMPR-sensitive Ara-C transporter that impacts the pharmacokinetic properties of this clinically important agent.

Indexed as

AnimalsAntimetabolites, AntineoplasticCytarabineDrug InteractionsEquilibrative Nucleoside Transporter 1FemaleHumansLeukemia, Myeloid, AcuteLiver-Specific Organic Anion Transporter 1MiceMice, KnockoutOrganic Cation Transport ProteinsSymportersThioinosine4-nitrobenzylthioinosineAntimetabolites, AntineoplasticCytarabineEquilibrative Nucleoside Transporter 1Liver-Specific Organic Anion Transporter 1MATE1 protein, mouseOrganic Cation Transport ProteinsSlc22a4 protein, mouseSLC29A1 protein, mouseSlco1b2 protein, mouseSymportersThioinosineacute myeloid leukemiacytarabineENT1NBMPROCTN1transporters

Identifiers

PMID31832201
PMCPMC6887677
OpenAlexW2992248754

What OpenQuestion 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 OpenQuestion graph.