Evidence map›Paper›PMID 31966054›Full record

ArticleOncology letters2020

BMP4 induces asymmetric cell division in human glioma stem-like cells.

Motofumi Koguchi, Yukiko Nakahara, Hiroshi Ito, Tomihiro Wakamiya, Fumitaka Yoshioka, Atsushi Ogata, Kohei Inoue, Jun Masuoka, Hideki Izumi, Tatsuya Abe

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2020. 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
0.9field-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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. A Novel Role of BIRC3 in Stemness Reprogramming of Glioblastoma.International journal of molecular sciences · 2021
    Article
  10. Article
  11. 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

10 authors at 2 institutions in 1 country.

Motofumi KoguchiDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Yukiko NakaharaDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Hiroshi ItoDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Tomihiro WakamiyaDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Fumitaka YoshiokaDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Atsushi OgataDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Kohei InoueDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Jun MasuokaDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Hideki IzumiLaboratory of Molecular Medicine, Life Sciences Institute, Saga Medical Center KOSEIKAN, Saga 840-8571, Japan.
Tatsuya AbeDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
Saga University · JPSaga-Ken Medical Centre Koseikan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is a malignant tumor with a high recurrence rate and has very poor prognosis in humans. The median survival is still <2 years. Therefore, a new treatment strategy should be established. Recently, this cancer has been thought to be heterogeneous, consisting of cancer stem cells (CSCs) that are self-renewable, multipotent, and treatment resistant. So various strategies targeting glioma stem-like cells (GSCs) have been investigated. This study focused on strategies targeting GSCs through the induction of differentiation using bone morphogenetic protein 4 (BMP4). The expression of CD133, a cancer stem cell marker, under BMP4 treatment in GSCs was examined using flow cytometry, western blotting, and quantitative PCR. Immunofluorescent staining of GSCs was also performed to examine the type of cell division: asymmetric cell division (ACD) or symmetric cell division (SCD). We obtained the following results. The BMP4 treatment caused downregulation of CD133 expression. Moreover, it induced ACD in GSCs. While the ACD ratio was 23% without BMP4 treatment, it was 38% with BMP4 treatment (P=0.004). Furthermore, the tumor sphere assay demonstrated that BMP4 suppresses self-renewal ability. In conclusion, these findings may provide a new perspective on how BMP4 treatment reduces the tumorigenicity of GSCs.

Indexed as

AC133asymmetric cell divisioncell differentiationglioblastomaneoplastic stem cell

Identifiers

PMID31966054
PMCPMC6956386
OpenAlexW2996734966

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.