Evidence map›Paper›PMID 29858061›Full record

ArticleMolecular therapy. Nucleic acids2018

Enhancing Electrotransfection Efficiency through Improvement in Nuclear Entry of Plasmid DNA.

Lisa D Cervia, Chun-Chi Chang, Liangli Wang, Mao Mao, Fan Yuan

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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  6. Internalization of transferrin-taggedExperimental biology and medicine (Maywood, N.J.) · 2024
    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

5 authors at 1 institution in 1 country.

Lisa D CerviaDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Chun-Chi ChangDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Liangli WangDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Mao MaoDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Fan YuanDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA. Electronic address: fyuan@duke.edu.
Duke University · US

Funding

Pharmacological Sciences Training ProgramT32GM007105 · NIGMS · DUKE UNIVERSITY · PI KUHN, CYNTHIA M · 1985 to 2019
$9.0M
Investigation of Endocytosis Involved in ElectrotransfectionR01GM098520 · NIGMS · DUKE UNIVERSITY · PI YUAN, FAN · 2013 to 2016
$1.2M
NIGMS NIH HHS R01 GM098520NIGMS NIH HHS T32 GM007105
6 · The paper itself

Abstract

The nuclear envelope is a physiological barrier to electrogene transfer. To understand different mechanisms of the nuclear entry for electrotransfected plasmid DNA (pDNA), the current study investigated how manipulation of the mechanisms could affect electrotransfection efficiency (eTE), transgene expression level (EL), and cell viability. In the investigation, cells were first synchronized at G2-M phase prior to electrotransfection so that the nuclear envelope breakdown (NEBD) occurred before pDNA entered the cells. The NEBD significantly increased the eTE and the EL while the cell viability was not compromised. In the second experiment, the cells were treated with a nuclear pore dilating agent (i.e., trans-1,2-cyclohexanediol). The treatment could increase the EL, but had only minor effects on eTE. Furthermore, the treatment was more cytotoxic, compared with the cell synchronization. In the third experiment, a nuclear targeting sequence (i.e., SV40) was incorporated into the pDNA prior to electrotransfection. The incorporation was more effective than the cell synchronization for enhancing the EL, but not the eTE, and the effectiveness was cell type dependent. Taken together, the data described above suggested that synchronization of the NEBD could be a practical approach to improving electrogene transfer in all dividing cells.

Indexed as

electroporationelectrotransfectionnuclear entrynuclear import

Identifiers

PMID29858061
PMCPMC5992438
OpenAlexW2794359118

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.