Evidence map›Paper›PMID 33494794›Full record

ArticleStem cell research & therapy2021

Dental pulp stem cells can improve muscle dysfunction in animal models of Duchenne muscular dystrophy.

Yuko Nitahara-Kasahara, Mutsuki Kuraoka, Posadas Herrera Guillermo, Hiromi Hayashita-Kinoh, Yasunobu Maruoka, Aki Nakamura-Takahasi, Koichi Kimura, Shin'ichi Takeda, Takashi Okada

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2021. 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
1.4field-weighted citation impact, top 19% 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, 18 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Article
  7. Stem Cell-Based Therapeutic Approaches in Genetic Diseases.Advances in experimental medicine and biology · 2023
    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

9 authors at 5 institutions in 1 country.

Yuko Nitahara-KasaharaDepartment of Biochemistry and Molecular Biology, Nippon Medical School, Tokyo, Japan. y-kasahara@nms.ac.jp.
Mutsuki KuraokaDepartment of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.
Posadas Herrera GuillermoDepartment of Biochemistry and Molecular Biology, Nippon Medical School, Tokyo, Japan.
Hiromi Hayashita-KinohDivision of Cell and Gene Therapy, Nippon Medical School, Bunkyo-city, Tokyo, Japan.
Yasunobu MaruokaDepartment of Biochemistry and Molecular Biology, Nippon Medical School, Tokyo, Japan.
Aki Nakamura-TakahasiDepartment of Pharmacology, Tokyo Dental College, Tokyo, Japan.
Koichi KimuraDepartment of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.
Shin'ichi TakedaDepartment of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.
Takashi OkadaDivision of Cell and Gene Therapy, Nippon Medical School, Bunkyo-city, Tokyo, Japan. t-okada@ims.u-tokyo.ac.jp.ORCID 0000-0002-2910-3797
National Center of Neurology and Psychiatry · JPNippon Medical School · JPNippon Veterinary and Life Science University · JPThe University of Tokyo · JPTokyo Dental College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDuchenne muscular dystrophy (DMD) is an inherited progressive disorder that causes skeletal and cardiac muscle deterioration with chronic inflammation. Dental pulp stem cells (DPSCs) are attractive candidates for cell-based strategies for DMD because of their immunosuppressive properties. Therefore, we hypothesized that systemic treatment with DPSCs might show therapeutic benefits as an anti-inflammatory therapy.

methodsTo investigate the potential benefits of DPSC transplantation for DMD, we examined disease progression in a DMD animal model, mdx mice, by comparing them with different systemic treatment conditions. The DPSC-treated model, a canine X-linked muscular dystrophy model in Japan (CXMD

resultsWe demonstrated a therapeutic strategy for long-term functional recovery in DMD using repeated DPSC administration. DPSC-treated mdx mice and CXMD

conclusionsWe developed a novel strategy for the safe and effective transplantation of DPSCs for DMD recovery, which included repeated systemic injection to regulate inflammation at a young age. This is the first report on the efficacy of a systemic DPSC treatment, from which we can propose that DPSCs may play an important role in delaying the DMD disease phenotype.

Indexed as

Muscular Dystrophy, DuchenneAnimalsDental PulpDisease Models, AnimalHumansMiceMice, Inbred mdxMuscle, SkeletalStem CellsAnti-inflammatory therapyDental pulp stem cellsDuchenne muscular dystrophy

Identifiers

PMID33494794
PMCPMC7831244
OpenAlexW3122765886

What Socratic 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 Socratic graph.