Evidence map›Paper›PMID 27748891›Full record

ArticleMolecular medicine reports2016

Hematopoietic stem cells as a tool for the treatment of glioblastoma multiforme.

Igor S Bryukhovetskiy, Inessa V Dyuizen, Valeriy E Shevchenko, Andrey S Bryukhovetskiy, Polina V Mischenko, Elena V Milkina, Yuri S Khotimchenko

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Stem cell therapies in the clinic.Bioengineering & translational medicine · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Cell therapies in the clinic.Bioengineering & translational medicine · 2021
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Vaccination in the immunotherapy of glioblastoma.Human vaccines & immunotherapeutics · 2018
    Review
  18. Review
  19. 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

7 authors at 1 institution in 1 country.

Igor S BryukhovetskiyFar Eastern Federal University, School of Biomedicine, Vladivostok 690091, Russia.
Inessa V DyuizenFar Eastern Federal University, School of Biomedicine, Vladivostok 690091, Russia.
Valeriy E ShevchenkoFar Eastern Federal University, School of Biomedicine, Vladivostok 690091, Russia.
Andrey S BryukhovetskiyFar Eastern Federal University, School of Biomedicine, Vladivostok 690091, Russia.
Polina V MischenkoFar Eastern Federal University, School of Biomedicine, Vladivostok 690091, Russia.
Elena V MilkinaFar Eastern Federal University, School of Biomedicine, Vladivostok 690091, Russia.
Yuri S KhotimchenkoFar Eastern Federal University, School of Biomedicine, Vladivostok 690091, Russia.
Far Eastern Federal University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme is an aggressive malignant brain tumor with terminal consequences. A primary reason for its resistance to treatment is associated with cancer stem cells (CSCs), of which there are currently no effective ways to destroy. It remains unclear what cancer cells become a target of stem cell migration, what the role of this process is in oncogenesis and what stem cell lines should be used in developing antitumor technologies. Using modern post‑genome technologies, the present study investigated the migration of human stem cells to cancer cells in vitro, the comparative study of cell proteomes of certain stem cells (including CSCs) was conducted and stem cell migration in vivo was examined. Of all glioblastoma cells, CSCs have the stability to attract normal stem cells. Critical differences in cell proteomes allow the consideration of hematopoietic stem cells (HSCs) as an instrument for interaction with glioblastoma CSCs. Following injection into the bloodstream of animals with glioblastoma, the majority of HSCs migrated to the tumor‑containing brain hemisphere and penetrated the tumor tissue. HSCs therefore are of potential use in the development of methods to target CSCs.

Indexed as

AnimalsCell Line, TumorCell MovementCell Transformation, NeoplasticDrug Resistance, NeoplasmGlioblastomaHematopoietic Stem CellsHumansNeoplasms, ExperimentalNeural Stem CellsProteomeRatsSignal TransductionProteome

Identifiers

PMID27748891
PMCPMC5101999
OpenAlexW2529992772

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.