Evidence map›Paper›PMID 29180963›Full record

ArticleFrontiers in pharmacology2017

Spinal Cord Molecular and Cellular Changes Induced by Adenoviral Vector- and Cell-Mediated Triple Gene Therapy after Severe Contusion.

Andrei A Izmailov, Tatyana V Povysheva, Farid V Bashirov, Mikhail E Sokolov, Filip O Fadeev, Ravil R Garifulin, Boris S Naroditsky, Denis Y Logunov, Ilnur I Salafutdinov, Yuri A Chelyshev and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

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  14. Combination of epidural electrical stimulation withNeural regeneration research · 2021
    Article
  15. Gene-modified leucoconcentrate for personalizedNeural regeneration research · 2021
    Article
  16. Article
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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

12 authors at 4 institutions in 2 countries.

Andrei A IzmailovDepartment of Biology, Kazan State Medical University, Kazan, Russia.
Tatyana V PovyshevaDepartment of Biology, Kazan State Medical University, Kazan, Russia.
Farid V BashirovDepartment of Biology, Kazan State Medical University, Kazan, Russia.
Mikhail E SokolovDepartment of Biology, Kazan State Medical University, Kazan, Russia.
Filip O FadeevDepartment of Biology, Kazan State Medical University, Kazan, Russia.
Ravil R GarifulinDepartment of Biology, Kazan State Medical University, Kazan, Russia.
Boris S NaroditskyGamaleya Research Institute of Epidemiology and Microbiology, Moscow, Russia.
Denis Y LogunovGamaleya Research Institute of Epidemiology and Microbiology, Moscow, Russia.
Ilnur I SalafutdinovInstitute of Fundamental Medicine and Biology, Kazan Federal (Volga Region) University, Kazan, Russia.
Yuri A ChelyshevDepartment of Biology, Kazan State Medical University, Kazan, Russia.
Rustem R IslamovDepartment of Biology, Kazan State Medical University, Kazan, Russia.
Igor A LavrovInstitute of Fundamental Medicine and Biology, Kazan Federal (Volga Region) University, Kazan, Russia.
Kazan State Medical University · RUGamalei Institute of Epidemiology and Microbiology · RUKazan Federal University · RUMayo Clinic in Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gene therapy has been successful in treatment of spinal cord injury (SCI) in several animal models, although it still remains unavailable for clinical practice. Surprisingly, regardless the fact that multiple reports showed motor recovery with gene therapy, little is known about molecular and cellular changes in the post-traumatic spinal cord following viral vector- or cell-mediated gene therapy. In this study we evaluated the therapeutic efficacy and changes in spinal cord after treatment with the genes encoding vascular endothelial growth factor (VEGF), glial cell-derived neurotrophic factor (GDNF), angiogenin (ANG), and neuronal cell adhesion molecule (NCAM) applied using both approaches. Therapeutic genes were used for viral vector- and cell-mediated gene therapy in two combinations: (1) VEGF+GDNF+NCAM and (2) VEGF+ANG+NCAM. For

Indexed as

angiogeningene therapyglial cell-derived neurotrophic factorglial cellshuman umbilical cord blood mononuclear cellneural cell adhesion moleculespinal cord injuryvascular endothelial growth factor

Identifiers

PMID29180963
PMCPMC5693893
OpenAlexW2768082937

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.