Evidence map›Paper›PMID 36835111›Full record

ArticleInternational journal of molecular sciences2023

NF-κB Decoy ODN-Loaded Poly(Lactic-co-glycolic Acid) Nanospheres Inhibit Alveolar Ridge Resorption.

Albert Chun-Shuo Huang, Yuji Ishida, Kai Li, Duantawan Rintanalert, Kasumi Hatano-Sato, Shuji Oishi, Jun Hosomichi, Risa Usumi-Fujita, Hiroyuki Yamaguchi, Hiroyuki Tsujimoto and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

14 authors at 3 institutions in 3 countries.

Albert Chun-Shuo HuangDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.ORCID 0000-0002-4710-032X
Yuji IshidaDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.ORCID 0000-0003-4973-8762
Kai LiDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.
Duantawan RintanalertDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.
Kasumi Hatano-SatoDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.
Shuji OishiDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.
Jun HosomichiDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.
Risa Usumi-FujitaDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.
Hiroyuki YamaguchiDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.ORCID 0000-0002-3754-6723
Hiroyuki TsujimotoPharmaceutical/Beauty Science Research Center, Material Business Division, Hosokawa Micron Corporation, Osaka 573-1132, Japan.
Aiko SasaiPharmaceutical/Beauty Science Research Center, Material Business Division, Hosokawa Micron Corporation, Osaka 573-1132, Japan.
Ayaka OchiPharmaceutical/Beauty Science Research Center, Material Business Division, Hosokawa Micron Corporation, Osaka 573-1132, Japan.
Hajime WatanabeAnGes Inc., Tokyo 108-0014, Japan.
Takashi OnoDepartment of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo 113-8549, Japan.ORCID 0000-0002-8043-660X
Tokyo Medical and Dental University · JPHosokawa Micron (Japan) · JPAnges (Japan) · JP

Funding

Grants-in-Aid for Scientific Research (20K18750) (KAKENHI), from the Japanese Ministry of Education, Culture, Sports, Science, and Technology, Japan (Kasumigaseki, Chiyoda-ku, Tokyo) 20K18750Joint research agreement with AnGes, Inc. and HOSOKAWA MICRON CORPORATION 21BA100275
6 · The paper itself

Abstract

Residual ridge resorption combined with dimensional loss resulting from tooth extraction has a prolonged correlation with early excessive inflammation. Nuclear factor-kappa B (NF-κB) decoy oligodeoxynucleotides (ODNs) are double-stranded DNA sequences capable of downregulating the expression of downstream genes of the NF-κB pathway, which is recognized for regulating prototypical proinflammatory signals, physiological bone metabolism, pathologic bone destruction, and bone regeneration. The aim of this study was to investigate the therapeutic effect of NF-κB decoy ODNs on the extraction sockets of Wistar/ST rats when delivered by poly(lactic-co-glycolic acid) (PLGA) nanospheres. Microcomputed tomography and trabecular bone analysis following treatment with NF-κB decoy ODN-loaded PLGA nanospheres (PLGA-NfDs) demonstrated inhibition of vertical alveolar bone loss with increased bone volume, smoother trabecular bone surface, thicker trabecular bone, larger trabecular number and separation, and fewer bone porosities. Histomorphometric and reverse transcription-quantitative polymerase chain reaction analysis revealed reduced tartrate-resistant acid phosphatase-expressing osteoclasts, interleukin-1β, tumor necrosis factor-α, receptor activator of NF-κB ligand, turnover rate, and increased transforming growth factor-β1 immunopositive reactions and relative gene expression. These data demonstrate that local NF-κB decoy ODN transfection via PLGA-NfD can be used to effectively suppress inflammation in a tooth-extraction socket during the healing process, with the potential to accelerate new bone formation.

Indexed as

Alveolar Bone LossNanospheresNF-kappa BPolylactic Acid-Polyglycolic Acid CopolymerAlveolar ProcessAnimalsGlycolsInflammationOligodeoxyribonucleotidesRatsRats, WistarX-Ray MicrotomographyGlycolsNF-kappa BNF-kappaB decoyOligodeoxyribonucleotidesPolylactic Acid-Polyglycolic Acid Copolymeralveolar bone lossbone remodelinginflammationnanosphereNF-κB transcription factor decoynuclear factor-kappa Boligodeoxynucleotidepoly(lactic-co-glycolic acid) copolymertooth extractionwound healing

Identifiers

PMID36835111
PMCPMC9962103
OpenAlexW4320492895

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.