Evidence map›Paper›PMID 26908439›Full record

ArticleOncotarget2016

The homing and inhibiting effects of hNSCs-BMP4 on human glioma stem cells.

Shuang Liu, Feng Yin, Mingming Zhao, Chunhui Zhou, Junlin Ren, Qiming Huang, Zhongming Zhao, Ramkrishna Mitra, Wenhong Fan, Ming Fan

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Regenerative Glycopeptide Scaffolds Enhance BMP-4 Activity To Treat Pediatric Glioma.Regenerative engineering and translational medicine · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Nanoparticles for Stem Cell Therapy Bioengineering in Glioma.Frontiers in bioengineering and biotechnology · 2020
    Review
  10. Emerging targets in cancer drug resistance.Cancer drug resistance (Alhambra, Calif.) · 2019
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. 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 4 institutions in 2 countries.

Shuang LiuDepartment of Neurosurgery, Navy General Hospital, PLA, Beijing 100048, China.
Feng YinDepartment of Neurosurgery, Navy General Hospital, PLA, Beijing 100048, China.
Mingming ZhaoDepartment of Neurosurgery, Navy General Hospital, PLA, Beijing 100048, China.
Chunhui ZhouDepartment of Neurosurgery, Navy General Hospital, PLA, Beijing 100048, China.
Junlin RenDepartment of Neurosurgery, Navy General Hospital, PLA, Beijing 100048, China.
Qiming HuangDepartment of Brain Protection & Plasticity Research, Beijing Institute of Basic Medical Sciences, Beijing 100850, China.
Zhongming ZhaoDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37203, USA.
Ramkrishna MitraDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37203, USA.
Wenhong FanNational Institutes for Food and Drug Control, Beijing 100050, China.
Ming FanDepartment of Brain Protection & Plasticity Research, Beijing Institute of Basic Medical Sciences, Beijing 100850, China.
PLA Navy General Hospital · CNChinese Institute for Brain Research · CNVanderbilt University Medical Center · USNational Institutes for Food and Drug Control · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant gliomas patients have a poor survival rate, partially due to the inability in delivering therapeutic agents to the tumors, especially to the metastasis of human glioma stem cells (hGSCs). To explore whether the human neural stem cells (hNSCs) with an over-expression of BMP4 (hNSCs-BMP4) can trace and inhibit hGSCs, in this study, we examined the migration of hNSCs to hGSCs using transwell assay in vitro and performed the fluorescent tracer experiment in vivo. We examined the proliferation, differentiation, apoptosis and migration of hGSCs after co-culturing with hNSCs-BMP4 in vitro and tested the tropism and antitumor effects of hNSCs-BMP4 in the established brain xenograft models of hGSCs. We found that hNSCs-BMP4 could secrete BMP4 and trace hGSCs both in vitro and in vivo. When compared to the normal human astrocytes (NHAs) and hNSCs, hNSCs-BMP4 could significantly inhibit the invasive growth of hGSCs, promote their differentiation and apoptosis by activating Smad1/5/8 signaling, and prolong the survival time of the tumor-bearing nude mice. Collectively, this study suggested that hNSCs-BMP4 may help in developing therapeutic approaches for the treatment of human malignant gliomas.

Indexed as

AnimalsBone Morphogenetic Protein 4Brain NeoplasmsFemaleGlioblastomaHeterograftsHumansMiceMice, NudeNeoplastic Stem CellsNeural Stem CellsBMP4 protein, humanBone Morphogenetic Protein 4BMP4homing effectshuman glioma stem cellshuman neural stem cellsinhibiting effects

Identifiers

PMID26908439
PMCPMC4951260
OpenAlexW2325508177

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.