Evidence map›Paper›PMID 32767051›Full record

ArticleBiochemical genetics2021

Polyprenol-Based Lipofecting Agents for In Vivo Delivery of Therapeutic DNA to Treat Hypertensive Rats.

Olga Gawrys, Monika Rak, Iwona Baranowska, Sylwia Bobis-Wozowicz, Karolina Szaro, Zbigniew Madeja, Ewa Swiezewska, Marek Masnyk, Marek Chmielewski, Elzbieta Karnas and 1 more

Abstract read
In one paragraph

Article in Biochemical genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Olga Gawrys *Department of Renal and Body Fluid Physiology, M. Mossakowski Medical Research Centre, PAS, 5 A. Pawinskiego Street, 02-106, Warsaw, Poland. olga.gawrys@gmail.com.ORCID http://orcid.org/0000-0002-4397-3991
Monika Rak *Department of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St., 30-387, Kraków, Poland.
Iwona BaranowskaDepartment of Renal and Body Fluid Physiology, M. Mossakowski Medical Research Centre, PAS, 5 A. Pawinskiego Street, 02-106, Warsaw, Poland.
Sylwia Bobis-WozowiczDepartment of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St., 30-387, Kraków, Poland.
Karolina SzaroDepartment of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St., 30-387, Kraków, Poland.
Zbigniew MadejaDepartment of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St., 30-387, Kraków, Poland.
Ewa SwiezewskaInstitute of Biochemistry and Biophysics, PAS, 5a A. Pawinskiego Street, 02-106, Warsaw, Poland.
Marek MasnykInstitute of Organic Chemistry, Polish Academy of Sciences, 44/52 M. Kasprzaka Street, 01-224, Warsaw, Poland.
Marek ChmielewskiInstitute of Organic Chemistry, Polish Academy of Sciences, 44/52 M. Kasprzaka Street, 01-224, Warsaw, Poland.
Elzbieta KarnasDepartment of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St., 30-387, Kraków, Poland.
Elzbieta Kompanowska-JezierskaDepartment of Renal and Body Fluid Physiology, M. Mossakowski Medical Research Centre, PAS, 5 A. Pawinskiego Street, 02-106, Warsaw, Poland.

Funding

Narodowe Centrum Nauki 2015/17/N/NZ4/02831
6 · The paper itself

Abstract

Development of efficient vectors for transfection is one of the major challenges in genetic engineering. Previous research demonstrated that cationic derivatives of polyisoprenoids (PTAI) may serve as carriers of nucleic acids. In the present study, the effectiveness of two PTAI-based formulations (PTAI-6-8 and 10-14) was investigated and compared to the commercial reagents. The purpose of applied gene therapy was to enhance the expression of vascular endothelial growth factor (VEGF-A) in the renal medulla of spontaneously hypertensive rats (SHR) and to test its potential as a novel antihypertensive intervention. In the first part of the study (in vitro), we confirmed that PTAI-based lipoplexes efficiently transfect XC rat sarcoma cells and are stable in 37 °C for 7 days. In the in vivo experiments, we administered selected lipoplexes directly to the kidneys of conscious SHR (via osmotic pumps). There were no blood pressure changes and VEGF-A level in renal medulla was significantly higher only for PTAI-10-14-based formulation. In conclusion, despite the promising results, we were not able to achieve VEGF-A expression level high enough to verify VEGF-A gene therapy usefulness in SHR. However, results of our study give important indications for the future development of PTAI-based DNA carriers and kidney-targeted gene delivery.

Indexed as

Genetic VectorsAnimalsBlood PressureCell Line, TumorDNAGenetic TherapyGlucoseHypertensionKidney MedullaMaleOsmosisPolyprenolsRatsRats, Inbred SHRTransfectionVascular Endothelial Growth Factor ADNAGlucosePolyprenolsVascular Endothelial Growth Factor ACationic derivatives of polyisoprenoid alcoholsHypertensionLipofectionSHRVEGF-A

Identifiers

PMID32767051
PMCPMC7846535

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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.