Evidence map›Paper›PMID 22038171›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2012

A novel hybrid promoter responsive to pathophysiological and pharmacological regulation.

Maria C Subang, Rewas Fatah, Carly Bright, Patricia Blanco, Mariana Berenstein, Ying Wu, Osvaldo L Podhajcer, Paul G Winyard, Yuti Chernajovsky, David Gould

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Gene doping: gene delivery for olympic victory.British journal of clinical pharmacology · 2013
    Review
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

10 authors at 4 institutions in 2 countries.

Maria C SubangBone and Joint Research Unit, Barts and The London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, Charterhouse Square, London, UK.
Rewas Fatah
Carly Bright
Patricia Blanco
Mariana Berenstein
Ying Wu
Osvaldo L Podhajcer
Paul G Winyard
Yuti Chernajovsky
David Gould
Queen Mary University of London · GBFundación Instituto Leloir · ARWilliam Harvey Research Institute · GBPeninsula College of Medicine and Dentistry · GB

Funding

Arthritis Research UK 17208Arthritis Research UK C0662Wellcome TrustWellcome Trust 071329/Z/03/Z
6 · The paper itself

Abstract

The aim of this study was to construct a promoter containing DNA motifs for an endogenous transcription factor associated with inflammation along with motifs for pharmacological regulation factors. We demonstrate in transfected cells that expression of a gene of interest is induced by hypoxic conditions or through pharmacological induction, and also show pharmacological repression. In vivo studies utilised electroporation of plasmid to mouse paws, a delivery method shown to be effective by bioluminescence imaging. For gene therapy, the promoter was used to drive expression of IL-1Ra in a paw inflammation model with therapeutic effect observed which was further enhanced when the promoter was additionally induced with a pharmacological activator. One of the most important observations from this study was that promoter induction by hypoxia or inflammation could be prevented by the pharmacological repressor in the absence of doxycycline. These studies demonstrate that hybrid promoters enable pharmacological adjustment to the pathophysiological level of gene expression and, importantly, that they allow termination of gene expression even in the presence of pathophysiological stimuli.

Indexed as

Promoter Regions, GeneticAnimalsCell HypoxiaCell LineGene Expression RegulationGenetic TherapyHumansInflammationInterleukin 1 Receptor Antagonist ProteinMaleMiceMice, Inbred BALB CNucleotide MotifsPlasmidsTetracyclinesTranscription FactorsInterleukin 1 Receptor Antagonist ProteinTetracyclinesTranscription Factors

Identifiers

PMID22038171
PMCPMC3308011
OpenAlexW2123203348

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.