Evidence map›Paper›PMID 22160381›Full record

ArticleBlood2012

Effects of tetrahydrouridine on pharmacokinetics and pharmacodynamics of oral decitabine.

Donald Lavelle, Kestis Vaitkus, Yonghua Ling, Maria A Ruiz, Reda Mahfouz, Kwok Peng Ng, Soledad Negrotto, Nicola Smith, Pramod Terse, Kory J Engelke and 4 more

Open access · bronzeAbstract readComparative StudyEvaluation Study
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Clinical Trials Assessing Hypomethylating Agents Combined with Other Therapies: Causes for Failure and Potential Solutions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
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  18. Exploring epigenetic and microRNA approaches for γ-globin gene regulation.Experimental biology and medicine (Maywood, N.J.) · 2021
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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

14 authors at 5 institutions in 1 country.

Donald LavelleDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Kestis Vaitkus
Yonghua Ling
Maria A Ruiz
Reda Mahfouz
Kwok Peng Ng
Soledad Negrotto
Nicola Smith
Pramod Terse
Kory J Engelke
Joseph Covey
Kenneth K Chan
Joseph Desimone
Yogen Saunthararajah
Cleveland Clinic · USNational Cancer Institute · USUniversity of Illinois Chicago · USJesse Brown VA Medical Center · USThe Ohio State University · US

Funding

Tailored education for informed preproductive decisions in sickle cell diseaseU54HL090513 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SAUNTHARARAJAH, YOGEN · 2008 to 2011
$4.5M
Optimizing decitabine regimen + formulation for nonDNA damaging DNMT1 depletionR01CA138858 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI SAUNTHARARAJAH, YOGEN · 2009 to 2013
$1.6M
NCI NIH HHS N01 CM042204NCI NIH HHS N01 CM052205NCI NIH HHS N01-CM-42204NCI NIH HHS N01-CM-52205NCI NIH HHS R01 CA138858NHLBI NIH HHS U54 HL090513NHLBI NIH HHS U54HL090513OCPHP CDC HHS PR081404
6 · The paper itself

Abstract

The deoxycytidine analog decitabine (DAC) can deplete DNA methyl-transferase 1 (DNMT1) and thereby modify cellular epigenetics, gene expression, and differentiation. However, a barrier to efficacious and accessible DNMT1-targeted therapy is cytidine deaminase, an enzyme highly expressed in the intestine and liver that rapidly metabolizes DAC into inactive uridine counterparts, severely limiting exposure time and oral bioavailability. In the present study, the effects of tetrahydrouridine (THU), a competitive inhibitor of cytidine deaminase, on the pharmacokinetics and pharmacodynamics of oral DAC were evaluated in mice and nonhuman primates. Oral administration of THU before oral DAC extended DAC absorption time and widened the concentration-time profile, increasing the exposure time for S-phase-specific depletion of DNMT1 without the high peak DAC levels that can cause DNA damage and cytotoxicity. THU also decreased interindividual variability in pharmacokinetics seen with DAC alone. One potential clinical application of DNMT1-targeted therapy is to increase fetal hemoglobin and treat hemoglobinopathy. Oral THU-DAC at a dose that would produce peak DAC concentrations of less than 0.2μM administered 2×/wk for 8 weeks to nonhuman primates was not myelotoxic, hypomethylated DNA in the γ-globin gene promoter, and produced large cumulative increases in fetal hemoglobin. Combining oral THU with oral DAC changes DAC pharmacology in a manner that may facilitate accessible noncytotoxic DNMT1-targeted therapy.

Indexed as

Administration, OralAnimalsAntimetabolitesAntimetabolites, AntineoplasticArea Under CurveAzacitidineBiological AvailabilityDecitabineDNA DamageDNA MethylationDrug InteractionsFemaleHematopoietic Stem CellsInactivation, MetabolicInjections, IntravenousInjections, SubcutaneousAntimetabolitesAntimetabolites, AntineoplasticAzacitidineDecitabineTetrahydrouridine

Identifiers

PMID22160381
PMCPMC3277356
OpenAlexW2113099773

What OpenQuestion holds

Textmetadata
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.