Evidence map›Paper›PMID 37693056›Full record

ArticleBioengineering & translational medicine2023

Gene therapy using genome-edited iPS cells for targeting malignant glioma.

Ryota Tamura, Hiroyuki Miyoshi, Kent Imaizumi, Masahiro Yo, Yoshitaka Kase, Tsukika Sato, Mizuto Sato, Yukina Morimoto, Oltea Sampetrean, Jun Kohyama and 6 more

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

  1. CRISPR-Based Gene Therapy for Brain Disease.Molecular neurobiology · 2026
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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

16 authors at 2 institutions in 1 country.

Ryota TamuraDepartment of Neurosurgery Keio University School of Medicine Shinjuku-ku, Tokyo Japan.ORCID https://orcid.org/0000-0002-8637-901X
Hiroyuki MiyoshiDepartment of Neurosurgery Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Kent ImaizumiDepartment of Physiology Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Masahiro YoLaboratory for Cell Function and Dynamics, RIKEN Center for Brain Science Wako, Saitama Japan.
Yoshitaka KaseDepartment of Physiology Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Tsukika SatoDepartment of Physiology Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Mizuto SatoDepartment of Neurosurgery Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Yukina MorimotoDepartment of Neurosurgery Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Oltea SampetreanDivision of Gene Regulation Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Jun KohyamaDepartment of Physiology Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Munehisa ShinozakiDepartment of Physiology Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Atsushi MiyawakiLaboratory for Cell Function and Dynamics, RIKEN Center for Brain Science Wako, Saitama Japan.
Kazunari YoshidaDepartment of Neurosurgery Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Hideyuki SayaDivision of Gene Regulation Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Hideyuki OkanoDepartment of Physiology Keio University School of Medicine Shinjuku-ku, Tokyo Japan.
Masahiro TodaDepartment of Neurosurgery Keio University School of Medicine Shinjuku-ku, Tokyo Japan.ORCID https://orcid.org/0000-0003-2700-1620
Keio University · JPRIKEN Center for Brain Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is characterized by diffuse infiltration into the normal brain. Invasive glioma stem cells (GSCs) are an underlying cause of treatment failure. Despite the use of multimodal therapies, the prognosis remains dismal. New therapeutic approach targeting invasive GSCs is required. Here, we show that neural stem cells (NSCs) derived from CRISRP/Cas9-edited human-induced pluripotent stem cell (hiPSC) expressing a suicide gene had higher tumor-trophic migratory capacity compared with mesenchymal stem cells (MSCs), leading to marked in vivo antitumor effects. High migratory capacity in iPSC-NSCs was related to self-repulsive action and pathotropism involved in EphB-ephrinB and CXCL12-CXCR4 signaling. The gene insertion to

Indexed as

CRISPR/Cas9ferroptosisgene therapyglioblastomamigration

Identifiers

PMID37693056
PMCPMC10487333
OpenAlexW4296270196

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.