Evidence map›Paper›PMID 28134617›Full record

ArticleeLife2017

Modeling susceptibility to drug-induced long QT with a panel of subject-specific induced pluripotent stem cells.

Francesca Stillitano, Jens Hansen, Chi-Wing Kong, Ioannis Karakikes, Christian Funck-Brentano, Lin Geng, Stuart Scott, Stephan Reynier, Ma Wu, Yannick Valogne and 8 more

Abstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

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  20. Spinal cord injury regulates circular RNA expression in axons.Frontiers in molecular neuroscience · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Francesca StillitanoCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Jens HansenDepartment of Pharmacology and Systems Therapeutics, Systems Biology Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Chi-Wing KongCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Ioannis KarakikesCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Christian Funck-BrentanoSorbonne Universités, UPMC Univ Paris 06, AP-HP, INSERM, CIC-1421, Institute of Cardiometabolism and Nutrition, Paris, France.
Lin GengCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Stuart ScottDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, United States.
Stephan ReynierCellectis Stem Cells, Paris, France.
Ma WuCellectis Stem Cells, Paris, France.
Yannick ValogneCellectis Stem Cells, Paris, France.
Carole DesseauxCellectis Stem Cells, Paris, France.
Joe-Elie SalemSorbonne Universités, UPMC Univ Paris 06, AP-HP, INSERM, CIC-1421, Institute of Cardiometabolism and Nutrition, Paris, France.
Dorota JeziorowskaSorbonne Universités, UPMC Univ Paris 06, AP-HP, INSERM, CIC-1421, Institute of Cardiometabolism and Nutrition, Paris, France.
Noël ZahrSorbonne Universités, UPMC Univ Paris 06, AP-HP, INSERM, CIC-1421, Institute of Cardiometabolism and Nutrition, Paris, France.
Ronald LiCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Ravi IyengarDepartment of Pharmacology and Systems Therapeutics, Systems Biology Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Roger J HajjarCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Jean-Sébastien HulotCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, United States.ORCID 0000-0001-5463-6117

Funding

System Biology Center in New YorkP50GM071558 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI IYENGAR, SRINIVAS RAVI V · 2007 to 2017
$22.8M
Drug Combination Signatures for Prediction and Mitigation of ToxicityU54HG008098 · NHGRI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BIRTWISTLE, MARC R., SOBIE, ERIC A · 2014 to 2019
$11.8M
MOLECULAR MECHANISM OF DESENSITIZATIONR01GM054508 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI IYENGAR, SRINIVAS RAVI V · 1995 to 2016
$8.0M
NHGRI NIH HHS U54 HG008098NIGMS NIH HHS P50 GM071558NIGMS NIH HHS R01 GM054508
6 · The paper itself

Abstract

A large number of drugs can induce prolongation of cardiac repolarization and life-threatening cardiac arrhythmias. The prediction of this side effect is however challenging as it usually develops in some genetically predisposed individuals with normal cardiac repolarization at baseline. Here, we describe a platform based on a genetically diverse panel of induced pluripotent stem cells (iPSCs) that reproduces susceptibility to develop a cardiotoxic drug response. We generated iPSC-derived cardiomyocytes from patients presenting in vivo with extremely low or high changes in cardiac repolarization in response to a pharmacological challenge with sotalol. In vitro, the responses to sotalol were highly variable but strongly correlated to the inter-individual differences observed in vivo. Transcriptomic profiling identified dysregulation of genes (

Indexed as

Anti-Arrhythmia AgentsArrhythmias, CardiacCardiotoxinsGene Expression ProfilingHumansInduced Pluripotent Stem CellsMass ScreeningModels, BiologicalResearch SubjectsAnti-Arrhythmia AgentsCardiotoxinsarrhythmiacardiotoxicityhumanhuman biologyinduced pluripotent stem cellsmedicine

Identifiers

PMID28134617
PMCPMC5279943

What OpenQuestion holds

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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.