Evidence map›Paper›PMID 25763123›Full record

ArticleKorean journal of urology2015

Optimizing in vivo gene transfer into mouse corpus cavernosum by use of surface electroporation.

Kang-Moon Song, Min Ji Choi, Mi-Hye Kwon, Kalyan Ghatak, Soo-Hwan Park, Dong-Soo Ryu, Ji-Kan Ryu, Jun-Kyu Suh

Open access · diamondAbstract read
In one paragraph

Article in Korean journal of urology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 2 institutions in 1 country.

Kang-Moon SongNational Research Center for Sexual Medicine and Department of Urology, Inha University School of Medicine, Incheon, Korea.
Min Ji ChoiNational Research Center for Sexual Medicine and Department of Urology, Inha University School of Medicine, Incheon, Korea.
Mi-Hye KwonNational Research Center for Sexual Medicine and Department of Urology, Inha University School of Medicine, Incheon, Korea.
Kalyan GhatakNational Research Center for Sexual Medicine and Department of Urology, Inha University School of Medicine, Incheon, Korea.
Soo-Hwan ParkNational Research Center for Sexual Medicine and Department of Urology, Inha University School of Medicine, Incheon, Korea.
Dong-Soo RyuDepartment of Urology, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea.
Ji-Kan RyuNational Research Center for Sexual Medicine and Department of Urology, Inha University School of Medicine, Incheon, Korea.
Jun-Kyu SuhNational Research Center for Sexual Medicine and Department of Urology, Inha University School of Medicine, Incheon, Korea.
Inha University · KRSamsung (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeElectroporation is known to enhance the efficiency of gene transfer through a transient increase in cell membrane permeability. The aim of this study was to determine the optimal conditions for in vivo electroporation-mediated gene delivery into mouse corpus cavernosum. MATERIALS AND

methodsDiabetes was induced in C57BL/6 mice by intraperitoneal injections of streptozotocin. After intracavernous injection of pCMV-Luc (100 µg/40 µL), different electroporation settings (5-50 V, 8-16 pulses with a duration of 40-100 ms) were applied to the penis to establish the optimal conditions for electroporation. Gene expression was evaluated by luciferase assay. We also assessed the undesired consequences of electroporation by visual inspection and hematoxylin-eosin staining of penile tissue.

resultsElectroporation profoundly induced gene expression in the corpus cavernosum tissue of normal mice in a voltage-dependent manner. We observed electrical burn scars in the penis of normal mice who received electroporation with eight 40-ms pulses at a voltage of 50 V and sixteen 40-ms pulses, eight 100-ms pulses, and sixteen 100-ms pulses at a voltage of 30 V. No detectable burn scars were noted in normal mice stimulated with eight 40-ms pulses at a voltage of 30 V. Electroporation also significantly induced gene expression in diabetic mice stimulated with 40-ms pulse at a voltage of 30 V without injury to the penis.

conclusionsWe have established the optimal electroporation conditions for maximizing gene transfer into the corpus cavernosum of mice while avoiding damage to the erectile tissue. The electroporation-mediated gene delivery technique will be a valuable tool for gene therapy in the field of erectile dysfunction.

Indexed as

AnimalsDiabetes Mellitus, ExperimentalElectroporationErectile DysfunctionGene ExpressionGenes, ReporterGenetic TherapyGene Transfer TechniquesLuciferasesMaleMiceMice, Inbred C57BLPenile ErectionPenisTransfectionLuciferasesElectroporationErectile dysfunctionGene therapyPenis

Identifiers

PMID25763123
PMCPMC4355430
OpenAlexW2134044131

What OpenQuestion holds

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LicenceCC BY-NC
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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.