Evidence map›Paper›PMID 29549271›Full record

ArticleScientific reports2018

Imaging of conditional gene silencing in vivo using a bioluminescence-based method with thermo-inducible microRNAs.

Karine Pinel, Coralie Genevois, Christelle Debeissat, Franck Couillaud

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 95% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 1 institution in 3 countries.

Karine PinelMolecular Imaging and Innovative Therapies (IMOTION), EA7435, Bordeaux, 33000, France. pinel.karine.m@gmail.com.
Coralie GenevoisMolecular Imaging and Innovative Therapies (IMOTION), EA7435, Bordeaux, 33000, France.ORCID 0000-0002-3208-1816
Christelle DebeissatMolecular Imaging and Innovative Therapies (IMOTION), EA7435, Bordeaux, 33000, France.
Franck CouillaudMolecular Imaging and Innovative Therapies (IMOTION), EA7435, Bordeaux, 33000, France. franck.couillaud@u-bordeaux.fr.ORCID 0000-0003-1324-2562
Université de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA interference (RNAi)-based gene therapy has great potential in cancer and infectious disease treatment to correct abnormal up-regulation of gene expression. We show a new original method uses synthetic microRNAs combined with a thermo-inducible promoter to reduce specific gene expression. The targeted gene is the luciferase firefly reporter gene overexpressed in a subcutaneous tumor which allows the RNAi monitoring by bioluminescence imaging (BLI). The inducible inhibition was first demonstrated in vitro using genetically modified cells lines and then in vivo using the corresponding xenograft model in mice. Achieving spatio-temporal control, we demonstrate the feasibility to induce, in vivo, a specific gene inhibition on demand. Future applications of this RNAi-based gene therapy, which can be restricted to pathological tissue, would offer wide-ranging potential for disease treatment.

Indexed as

FeverGene SilencingLuminescent MeasurementsAnimalsFemaleGlioblastomaHSP70 Heat-Shock ProteinsHumansLuciferases, FireflyMiceMice, Inbred NODMice, SCIDMicroRNAsOptical ImagingPromoter Regions, GeneticRNA, Small InterferingHSP70 Heat-Shock ProteinsHSPA7 protein, humanLuciferases, FireflyMicroRNAsRNA, Small Interfering

Identifiers

PMID29549271
PMCPMC5856835
OpenAlexW2806312458

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.