Evidence map›Paper›PMID 33353116›Full record

ArticlePharmaceutics2020

Therapeutic Angiogenesis by a "Dynamic Duo": Simultaneous Expression of HGF and VEGF165 by Novel Bicistronic Plasmid Restores Blood Flow in Ischemic Skeletal Muscle.

Ekaterina Slobodkina, Maria Boldyreva, Maxim Karagyaur, Roman Eremichev, Natalia Alexandrushkina, Vadim Balabanyan, Zhanna Akopyan, Yelena Parfyonova, Vsevolod Tkachuk, Pavel Makarevich

Abstract read
In one paragraph

Article in Pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

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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

10 authors.

Ekaterina SlobodkinaFaculty of Medicine, Lomonosov Moscow State University, 117192 Moscow, Russia.
Maria BoldyrevaNational Medical Research Center of Cardiology Russian Ministry of Health, 121552 Moscow, Russia.ORCID 0000-0002-8309-0018
Maxim KaragyaurFaculty of Medicine, Lomonosov Moscow State University, 117192 Moscow, Russia.
Roman EremichevInstitute for Regenerative Medicine, Medical Research and Education Centre, Lomonosov Moscow State University, 119192 Moscow, Russia.
Natalia AlexandrushkinaFaculty of Medicine, Lomonosov Moscow State University, 117192 Moscow, Russia.
Vadim BalabanyanFaculty of Medicine, Lomonosov Moscow State University, 117192 Moscow, Russia.
Zhanna AkopyanFaculty of Medicine, Lomonosov Moscow State University, 117192 Moscow, Russia.
Yelena ParfyonovaFaculty of Medicine, Lomonosov Moscow State University, 117192 Moscow, Russia.ORCID 0000-0001-8869-5190
Vsevolod TkachukFaculty of Medicine, Lomonosov Moscow State University, 117192 Moscow, Russia.
Pavel MakarevichFaculty of Medicine, Lomonosov Moscow State University, 117192 Moscow, Russia.ORCID 0000-0003-4946-7843

Funding

Presidential grant MK-1068.2019.7Russian Foundation for Basic Research 20-015-00181
6 · The paper itself

Abstract

Therapeutic angiogenesis is a promising strategy for relief of ischemic conditions, and gene delivery was used to stimulate blood vessels' formation and growth. We have previously shown that intramuscular injection of a mixture containing plasmids encoding vascular endothelial growth factor (VEGF)165 and hepatocyte growth factor (HGF) leads to restoration of blood flow in mouse ischemic limb, and efficacy of combined delivery was superior to each plasmid administered alone. In this work, we evaluated different approaches for co-expression of HGF and VEGF165 genes in a panel of candidate plasmid DNAs (pDNAs) with internal ribosome entry sites (IRESs), a bidirectional promoter or two independent promoters for each gene of interest. Studies in HEK293T culture showed that all plasmids provided synthesis of HGF and VEGF165 proteins and stimulated capillary formation by human umbilical vein endothelial cells (HUVEC), indicating the biological potency of expressed factors. Tests in skeletal muscle explants showed a dramatic difference and most plasmids failed to express HGF and VEGF165 in a significant quantity. However, a bicistronic plasmid with two independent promoters (cytomegalovirus (CMV) for HGF and chicken b-actin (CAG) for VEGF165) provided expression of both grow factors in skeletal muscle at an equimolar ratio. Efficacy tests of bicistronic plasmid were performed in a mouse model of hind limb ischemia. Intramuscular administration of plasmid induced significant restoration of perfusion compared to an empty vector and saline. These findings were supported by increased CD31+ capillary density in animals that received pHGF/VEGF. Overall, our study reports a first-in-class candidate gene therapy drug to deliver two pivotal angiogenic growth factors (HGF and VEGF165) with properties that provide basis for future development of treatment for an unmet medical need-peripheral artery disease and associated limb ischemia.

Indexed as

angiogenic growth factorsbicistronic vectorgene therapyHGFlimb ischemiaplasmidstherapeutic angiogenesisVEGF

Identifiers

PMID33353116
PMCPMC7766676

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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.