Evidence map›Paper›PMID 30089353›Full record

ArticleEuropean journal of histochemistry : EJH2018

Analysis of mineral apposition rates during alveolar bone regeneration over three weeks following transfer of BMP-2/7 gene via in vivo electroporation

Mariko Kawai, Yohei Kataoka, Junya Sonobe, Hiromitsu Yamamoto, Hiroki Maruyama, Toshio Yamamoto, Kazuhisa Bessho, Kiyoshi Ohura

Open access · goldAbstract read
In one paragraph

Article in European journal of histochemistry : EJH, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Potential Role of BMP7 in Regenerative Dentistry.International dental journal · 2024
    Review
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Non-viral Gene Delivery Methods for Bone and Joints.Frontiers in bioengineering and biotechnology · 2020
    Review
  10. Article
  11. Article
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 4 institutions in 2 countries.

Mariko KawaiOsaka Dental University, Department of Pharmacology, Japan.
Yohei KataokaOkayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Department of Oral Morphology, Japan.
Junya SonobeDepartment of Oral and Maxillofacial Surgery, Kyoto University, Japan.
Hiromitsu YamamotoDepartment of Oral and Maxillofacial Surgery, Kyoto University, Japan.
Hiroki MaruyamaNiigata University Graduate School of Medicine and Dental Sciences, Department of Clinical Nephroscience, Japan.
Toshio YamamotoOkayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Department of Oral Morphology, Japan.
Kazuhisa BesshoDepartment of Oral and Maxillofacial Surgery, Kyoto University, Japan.
Kiyoshi OhuraOsaka Dental University, Department of Pharmacology, Japan.
Kyoto University · JPOkayama University · JPOsaka Dental University · JPNiigata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alveolar bone is not spontaneously regenerated following trauma or periodontitis. We previously proposed an animal model for new alveolar bone regeneration therapy based on the non-viral BMP-2/7 gene expression vector and in vivo electroporation, which induced the formation of new alveolar bone over the course of a week. Here, we analysed alveolar bone during a period of three weeks following gene transfer to periodontal tissue. Non-viral plasmid vector pCAGGS-BMP-2/7 or pCAGGS control was injected into palatal periodontal tissue of the first molar of the rat maxilla and immediately electroporated with 32 pulses of 50 V for 50 msec. Over the following three weeks, rats were double bone-stained by calcein and tetracycline every three days and mineral apposition rates (MAR) were measured. Double bone-staining revealed that MAR of alveolar bone was as similar level three days before BMP-2/7 gene transfer as three days after gene transfer. However, from 3 to 6 days, 6 to 9 days, 9 to 12 days, 12 to 15 days, 15 to 18 days, and 18 to 20 days after, MARs were significantly higher than prior to gene transfer. Our proposed gene therapy for alveolar bone regeneration combining non-viral BMP-2/7 gene expression vector and in vivo electroporation could increase alveolar bone regeneration potential in the targeted area for up to three weeks.

Indexed as

Bone RegenerationAnimalsBone Morphogenetic Protein 2Bone Morphogenetic Protein 7ElectroporationGene ExpressionGene Transfer TechniquesMaleRatsRats, Inbred WFStaining and LabelingBMP2 protein, humanBMP7 protein, humanBone Morphogenetic Protein 2Bone Morphogenetic Protein 7

Identifiers

PMID30089353
PMCPMC6119816
OpenAlexW2885416408

What OpenQuestion holds

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LicenceCC BY-NC
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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.