Evidence map›Paper›PMID 27877903›Full record

ArticleScience and technology of advanced materials2016

The novel functional nucleic acid iRed effectively regulates target genes following cytoplasmic delivery by faint electric treatment.

Mahadi Hasan, Noriko Tarashima, Koki Fujikawa, Takashi Ohgita, Susumu Hama, Tamotsu Tanaka, Hiroyuki Saito, Noriaki Minakawa, Kentaro Kogure

Open access · goldAbstract read
In one paragraph

Article in Science and technology of advanced materials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Mahadi HasanDepartment of Biophysical Chemistry, Kyoto Pharmaceutical University , Kyoto , Japan.
Noriko TarashimaTokushima University Graduate School of Biomedical Sciences , Tokushima , Japan.
Koki FujikawaTokushima University Graduate School of Biomedical Sciences , Tokushima , Japan.
Takashi OhgitaDepartment of Biophysical Chemistry, Kyoto Pharmaceutical University , Kyoto , Japan.
Susumu HamaDepartment of Biophysical Chemistry, Kyoto Pharmaceutical University , Kyoto , Japan.
Tamotsu TanakaTokushima University Graduate School of Biomedical Sciences , Tokushima , Japan.
Hiroyuki SaitoDepartment of Biophysical Chemistry, Kyoto Pharmaceutical University , Kyoto , Japan.
Noriaki MinakawaTokushima University Graduate School of Biomedical Sciences , Tokushima , Japan.
Kentaro KogureTokushima University Graduate School of Biomedical Sciences , Tokushima , Japan.
Tokushima University · JPKyoto Pharmaceutical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An intelligent shRNA expression device (iRed) contains the minimum essential components needed for shRNA production in cells, and could be a novel tool to regulate target genes. However, general delivery carriers consisting of cationic polymers/lipids could impede function of a newly generated shRNA via electrostatic interaction in the cytoplasm. Recently, we found that faint electric treatment (fET) of cells enhanced delivery of siRNA and functional nucleic acids into the cytoplasm in the absence of delivery carriers. Here, we examined fET of cells stably expressing luciferase in the presence of iRed encoding anti-luciferase shRNA. Transfection of lipofectamine 2000 (LFN)/iRed lipoplexes showed an RNAi effect, but fET-mediated iRed transfection did not, likely because of the endosomal localization of iRed after delivery. However, fET in the presence of lysosomotropic agent chloroquine significantly improved the RNAi effect of iRed/fET to levels that were higher than those for the LFN/iRed lipoplexes. Furthermore, the amount of lipid droplets in adipocytes significantly decreased following fET with iRed against resistin in the presence of chloroquine. Thus, iRed could be a useful tool to regulate target genes following fET-mediated cytoplasmic delivery with endosomal escape devices.

Indexed as

211 Scaffold / Tissue engineering / Drug delivery30 Bio-inspired and biomedical materials4′-thioDNA600 Others: Nucleic acidscytoplasmic deliveryfaint electric treatmentiRedRNAi effect

Identifiers

PMID27877903
PMCPMC5111564
OpenAlexW2519859983

What OpenQuestion holds

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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.