Evidence map›Paper›PMID 28362377›Full record

ArticleJournal of visualized experiments : JoVE2017

A Fluorescence-based Lymphocyte Assay Suitable for High-throughput Screening of Small Molecules.

Ahmed Fouda, Mahasti Tahsini, Fatemeh Khodayarian, Fatimah Al-Nafisah, Moutih Rafei

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 44% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  3. TheiScience · 2022
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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

5 authors at 1 institution in 1 country.

Ahmed FoudaDepartment of Microbiology, Infectiology and Immunology, Université de Montréal.
Mahasti TahsiniDepartment of Pharmacology and Physiology, Université de Montréal.
Fatemeh KhodayarianDepartment of Pharmacology and Physiology, Université de Montréal.
Fatimah Al-NafisahDepartment of Pharmacology and Physiology, Université de Montréal.
Moutih RafeiDepartment of Microbiology, Infectiology and Immunology, Université de Montréal; Department of Pharmacology and Physiology, Université de Montréal; Molecular Biology Program, Université de Montréal; moutih.rafei.1@umontreal.ca.
Université de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput screening (HTS) is currently the mainstay for the identification of chemical entities capable of modulating biochemical reactions or cellular processes. With the advancement of biotechnologies and the high translational potential of small molecules, a number of innovative approaches in drug discovery have evolved, which explains the resurgent interest in the use of HTS. The oncology field is currently the most active research area for drug screening, with no major breakthrough made for the identification of new immunomodulatory compounds targeting transplantation-related complications or autoimmune ailments. Here, we present a novel in vitro murine fluorescent-based lymphocyte assay easily adapted for the identification of new immunomodulatory compounds. This assay uses T or B cells derived from a transgenic mouse, in which the Nur77 promoter drives GFP expression upon T- or B-cell receptor stimulation. As the GFP intensity reflects the activation/transcriptional activity of the target cell, our assay defines a novel tool to study the effect of given compound(s) on cellular/biological responses. For instance, a primary screening was performed using 4,398 compounds in the absence of a "target hypothesis", which led to the identification of 160 potential hits displaying immunomodulatory activities. Thus, the use of this assay is suitable for drug discovery programs exploring large chemical libraries prior to further in vitro/in vivo validation studies.

Indexed as

AnimalsBiological AssayDrug Evaluation, PreclinicalFemaleFlow CytometryFluorescenceGreen Fluorescent ProteinsHigh-Throughput Screening AssaysHumansImmunologic FactorsLymphocytesMice, TransgenicNuclear Receptor Subfamily 4, Group A, Member 1Receptors, Antigen, T-CellSmall Molecule LibrariesGreen Fluorescent ProteinsImmunologic FactorsNr4a1 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 1Receptors, Antigen, T-CellSmall Molecule Libraries

Identifiers

PMID28362377
PMCPMC5409279
OpenAlexW2594876907

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.