Evidence map›Paper›PMID 28027448›Full record

ArticleSLAS discovery : advancing life sciences R & D2017

Induced Pluripotent HD Monkey Stem Cells Derived Neural Cells for Drug Discovery.

Tanut Kunkanjanawan, Richard Carter, Kwan-Sung Ahn, Jinjing Yang, Rangsun Parnpai, Anthony W S Chan

Open access · hybridAbstract read
In one paragraph

Article in SLAS discovery : advancing life sciences R & D, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
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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

6 authors at 3 institutions in 2 countries.

Tanut Kunkanjanawan1 Yerkes National Primate Research Center, Atlanta, GA, USA.
Richard Carter1 Yerkes National Primate Research Center, Atlanta, GA, USA.
Kwan-Sung Ahn1 Yerkes National Primate Research Center, Atlanta, GA, USA.
Jinjing Yang1 Yerkes National Primate Research Center, Atlanta, GA, USA.
Rangsun Parnpai3 Embryo Technology and Stem Cell Research Center, School of Biotechnology, Suranaree University of Technology, Nakhon Ratchasima, Thailand.
Anthony W S Chan1 Yerkes National Primate Research Center, Atlanta, GA, USA.
Emory National Primate Research CenterEmory University · USSuranaree University of Technology · TH

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 1985 to 2011
$114.0M
Establishment of a transgenic monkey of Huntingtons's dieseaseR24RR018827 · NCRR · EMORY UNIVERSITY · PI CHAN, ANTHONY WING SANG · 2004 to 2011
$6.2M
Transgenic Huntington's disease monkey resourceR24OD010930 · OD · EMORY UNIVERSITY · PI CHAN, ANTHONY WING SANG · 2012 to 2018
$6.1M
A gene and prgenitor cell therapy in Huntington disease miceR21NS084163 · NINDS · EMORY UNIVERSITY · PI CHAN, ANTHONY WING SANG · 2013 to 2014
$427k
NCRR NIH HHS P51 RR000165NCRR NIH HHS R24 RR018827NIH HHS P51 OD011132NIH HHS R24 OD010930NINDS NIH HHS R21 NS084163
6 · The paper itself

Abstract

Huntington's disease (HD) is a neurodegenerative disease caused by an expansion of CAG trinucleotide repeat (polyglutamine [polyQ]) in the huntingtin ( HTT) gene, which leads to the formation of mutant HTT (mHTT) protein aggregates. In the nervous system, an accumulation of mHTT protein results in glutamate-mediated excitotoxicity, proteosome instability, and apoptosis. Although HD pathogenesis has been extensively studied, effective treatment of HD has yet to be developed. Therapeutic discovery research in HD has been reported using yeast, cells derived from transgenic animal models and HD patients, and induced pluripotent stem cells from patients. A transgenic nonhuman primate model of HD (HD monkey) shows neuropathological, behavioral, and molecular changes similar to an HD patient. In addition, neural progenitor cells (NPCs) derived from HD monkeys can be maintained in culture and differentiated to neural cells with distinct HD cellular phenotypes including the formation of mHTT aggregates, intranuclear inclusions, and increased susceptibility to oxidative stress. Here, we evaluated the potential application of HD monkey NPCs and neural cells as an in vitro model for HD drug discovery research.

Indexed as

Drug DiscoveryAnimalsApoptosisCell DifferentiationCells, CulturedCell SurvivalDisease Models, AnimalGlucosephosphate DehydrogenaseHuntingtin ProteinHuntington DiseaseInduced Pluripotent Stem CellsMacaca mulattaNeural Stem CellsProtein AggregatesProtein Aggregation, PathologicalGlucosephosphate DehydrogenaseHuntingtin ProteinProtein Aggregatesdrug screeningHuntington’s diseasemonkey modelneural cellspluripotent stem cells

Identifiers

PMID28027448
PMCPMC5699456
OpenAlexW2582789119

What OpenQuestion holds

Textmetadata
LicenceTDM
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.