Evidence map›Paper›PMID 29435139›Full record

ArticleOncotarget2018

Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.

Min Shen, Rosita Asawa, Ya-Qin Zhang, Elizabeth Cunningham, Hongmao Sun, Alexander Tropsha, William P Janzen, Eugene N Muratov, Stephen J Capuzzi, Sherif Farag and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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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.

Min ShenNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
Rosita AsawaNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
Ya-Qin ZhangNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
Elizabeth CunninghamNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
Hongmao SunNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
Alexander TropshaLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
William P JanzenEpizyme, Inc., Cambridge, MA, USA.
Eugene N MuratovEshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA.
Stephen J CapuzziEshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA.
Sherif FaragEshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA.
Ajit JadhavNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
Julie BlattDivision of Pediatric Hematology Oncology, University of North Carolina, Chapel Hill, NC, USA.
Anton SimeonovNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
Natalia J MartinezNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
National Center for Advancing Translational Sciences · USNational Institutes of Health · USUniversity of North Carolina at Chapel Hill · USEpizyme (United States) · USUNC Lineberger Comprehensive Cancer Center

Funding

Drug Repurposing for Cancer Therapy: From Man to Molecules to ManU01CA207160 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TROPSHA, ALEXANDER · 2016 to 2018
$1.2M
NCI NIH HHS U01 CA207160
6 · The paper itself

Abstract

Drug repurposing approaches have the potential advantage of facilitating rapid and cost-effective development of new therapies. Particularly, the repurposing of drugs with known safety profiles in children could bypass or streamline toxicity studies. We employed a phenotypic screening paradigm on a panel of well-characterized cell lines derived from pediatric solid tumors against a collection of ∼3,800 compounds spanning approved drugs and investigational agents. Specifically, we employed titration-based screening where compounds were tested at multiple concentrations for their effect on cell viability. Molecular and cellular target enrichment analysis indicated that numerous agents across different therapeutic categories and modes of action had an antiproliferative effect, notably antiparasitic/protozoal drugs with non-classic antineoplastic activity. Focusing on active compounds with dosing and safety information in children according to the Children's Pharmacy Collaborative database, we identified compounds with therapeutic potential through further validation using 3D tumor spheroid models. Moreover, we show that antiparasitic agents induce cell death

Indexed as

3D culturesdrug repurposingpediatric cancerquantitative high-throughput screening

Identifiers

PMID29435139
PMCPMC5797010
OpenAlexW2778947919

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.