Evidence map›Paper›PMID 35514421›Full record

ArticleRSC advances2020

Synthesis of siRNAs incorporated with cationic peptides R8G7 and R8A7 and the effect of the modifications on siRNA properties.

Miho Matsubara, Kenji Honda, Koki Ozaki, Ryohei Kajino, Yuri Kakisawa, Yusuke Maeda, Yoshihito Ueno

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2020. 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
0.1field-weighted citation impact, top 55% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

7 authors at 2 institutions in 3 countries.

Miho MatsubaraCourse of Applied Life Science, Faculty of Applied Biological Sciences, Gifu University 1-1 Yanagido Gifu 501-1193 Japan uenoy@gifu-u.ac.jp +81-58-293-2919 +81-58-293-2919.
Kenji HondaCourse of Applied Life Science, Faculty of Applied Biological Sciences, Gifu University 1-1 Yanagido Gifu 501-1193 Japan uenoy@gifu-u.ac.jp +81-58-293-2919 +81-58-293-2919.
Koki OzakiCourse of Applied Life Science, Faculty of Applied Biological Sciences, Gifu University 1-1 Yanagido Gifu 501-1193 Japan uenoy@gifu-u.ac.jp +81-58-293-2919 +81-58-293-2919.
Ryohei KajinoUnited Graduate School of Agricultural Science, Gifu University 1-1 Yanagido Gifu 501-1193 Japan.
Yuri KakisawaCourse of Applied Life Science, Faculty of Applied Biological Sciences, Gifu University 1-1 Yanagido Gifu 501-1193 Japan uenoy@gifu-u.ac.jp +81-58-293-2919 +81-58-293-2919.
Yusuke MaedaCourse of Applied Life Science, Faculty of Applied Biological Sciences, Gifu University 1-1 Yanagido Gifu 501-1193 Japan uenoy@gifu-u.ac.jp +81-58-293-2919 +81-58-293-2919.
Yoshihito UenoCourse of Applied Life Science, Faculty of Applied Biological Sciences, Gifu University 1-1 Yanagido Gifu 501-1193 Japan uenoy@gifu-u.ac.jp +81-58-293-2919 +81-58-293-2919.ORCID https://orcid.org/0000-0003-3492-4677
Faculty (United Kingdom) · GBGifu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small interfering RNA (siRNA) can be used as an innovative next-generation drug. However, there are several challenges in the therapeutic application of siRNAs, including their low cell membrane permeability. In this study, we designed and synthesized siRNAs, incorporating the cationic peptides R8G7 and R8A7 to improve cell membrane permeability of siRNAs. Thermal denaturation studies revealed that R8G7 and R8A7 modifications increased the thermal stability of the siRNA duplexes. Incorporating these peptides at the 3'-ends of the siRNA passenger strands increased the stability of the siRNAs in a buffer containing bovine serum. Further, we found that the peptide-siRNA conjugates did not show sufficient RNA interference (RNAi) activity in the absence of the transfection reagent; however, when the transfection reagent was used, the peptide-siRNA conjugates preserved their RNAi activity.

Identifiers

PMID35514421
PMCPMC9056854
OpenAlexW3087199183

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.