Evidence map›Paper›PMID 26439843›Full record

ArticleSpinal cord2016

Construction of recombinant adenovirus containing picorna-viral 2A-peptide sequence for the co-expression of neuro-protective growth factors in human umbilical cord blood cells.

E E Garanina, Y O Mukhamedshina, I I Salafutdinov, A P Kiyasov, L M Lima, H J Reis, A Palotás, R R Islamov, A A Rizvanov

Open access · bronzeAbstract read
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Article in Spinal cord, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-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

4 citing papers in PubMed, 9 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

9 authors at 5 institutions in 3 countries.

E E GaraninaKazan Federal University, Kazan, Russian Federation.
Y O MukhamedshinaKazan Federal University, Kazan, Russian Federation.
I I SalafutdinovKazan Federal University, Kazan, Russian Federation.
A P KiyasovKazan Federal University, Kazan, Russian Federation.
L M LimaUniversidade Federal de Viçosa, Viçosa, Brazil.
H J ReisUniversidade Federal de Minas Gerais, Belo Horizonte, Brazil.
A PalotásKazan Federal University, Kazan, Russian Federation.
R R IslamovKazan State Medical University, Kazan, Russian Federation.
A A RizvanovKazan Federal University, Kazan, Russian Federation.
Kazan Federal University · RUAsklepios · HUKazan State Medical University · RUUniversidade Federal de Minas Gerais · BRUniversidade Federal de Viçosa · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

STUDY

designExperimental study.

objectiveSeveral neuro-degenerative disorders such as Alzheimer's dementia, Parkinson's disease and amyotrophic lateral sclerosis (ALS) are associated with genetic mutations, and replacing or disrupting defective sequences might offer therapeutic benefits. Single gene delivery has so far failed to achieve significant clinical improvements in humans, leading to the advent of co-expression of multiple therapeutic genes. Co-transfection using two or more individual constructs might inadvertently result in disproportionate delivery of the products into the cells. To prevent this, and in order to rule out interference among the many promoters with varying strength, expressing multiple proteins in equimolar amounts can be achieved by linking open reading frames under the control of only one promoter.

settingKazan, Russian Federation.

methodsHere we describe a strategy for adeno-viral co-expression of vascular endothelial growth factor (VEGF) and fibroblast growth factor 2 (FGF2) interconnected through picorna-viral 2A-amino-acid sequence in transfected human umbilical cord blood mono-nuclear cells (hUCB-MCs).

resultsPresence of both growth factors, as well as absence of immune response to 2A-antigen, was demonstrated after 28-52 days. Following injection of hUCB-MCs into ALS transgenic mice, co-expression of VEGF and FGF2, as well as viable xeno-transplanted cells, were observed in the spinal cord after 1 month.

conclusionThese results suggest that recombinant adeno-virus containing 2A-sequences could serve as a promising alternative in regenerative medicine for the delivery of therapeutic molecules to treat neurodegenerative diseases, such as ALS.

Indexed as

AdenoviridaeAmyotrophic Lateral SclerosisAnimalsBlood CellsCysteine EndopeptidasesDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFetal BloodFibroblast Growth Factor 2Genetic VectorsHEK293 CellsHumansMaleMiceMice, TransgenicMutationCysteine EndopeptidasesFibroblast Growth Factor 2picornain 2A, PicornavirusRecombinant ProteinsSuperoxide Dismutase-1Vascular Endothelial Growth Factor AViral Proteins

Identifiers

PMID26439843
OpenAlexW1856582230

What OpenQuestion holds

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Registered trials

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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.